Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 221154 |
| ensemblid | ENSG00000165487.14 |
| hgncid | 31830 |
| symbol | MICU2 |
| name | mitochondrial calcium uptake 2 |
| refseq_nuc | NM_152726.3 |
| refseq_prot | NP_689939.1 |
| ensembl_nuc | ENST00000382374.9 |
| ensembl_prot | ENSP00000371811.4 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 21492691 |
| end | 21604170 |
| strand | - |
| ver | v1.2 |
| region | chr13:21492691-21604170 |
| region5000 | chr13:21487691-21609170 |
| regionname0 | MICU2_chr13_21492691_21604170 |
| regionname5000 | MICU2_chr13_21487691_21609170 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 434 | 312 | 91 | 63 | 106 | 16 | 34 | 82 | MICU2_chr13_21487691_21609170 | MICU2 | MAAAA others(429): Show |
chr13 | 21487691 | 21609170 |
| a0002 | 0/0 | 434 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | MAAAA others(429): Show |
chr13 | 21487691 | 21609170 |
| a0003 | 0/0 | 434 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | MAAAA others(429): Show |
chr13 | 21487691 | 21609170 |
| a0004 | 0/0 | 434 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | MAAAA others(429): Show |
chr13 | 21487691 | 21609170 |
| a0005 | 0/0 | 434 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | MAAAA others(429): Show |
chr13 | 21487691 | 21609170 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1302 | 265 | 67 | 53 | 106 | 10 | 27 | MICU2_chr13_21487691_21609170 | MICU2 | ATGGC others(1297): Show |
chr13 | 21487691 | 21609170 | ||
| a0001c0002 | 0/0 | 1302 | 23 | 21 | 2 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | ATGGC others(1297): Show |
chr13 | 21487691 | 21609170 | ||
| a0001c0003 | 0/0 | 1302 | 22 | 2 | 8 | 0 | 6 | 6 | MICU2_chr13_21487691_21609170 | MICU2 | ATGGC others(1297): Show |
chr13 | 21487691 | 21609170 | ||
| a0001c0006 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | ATGGC others(1297): Show |
chr13 | 21487691 | 21609170 | ||
| a0001c0008 | 0/0 | 1302 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | ATGGC others(1297): Show |
chr13 | 21487691 | 21609170 | ||
| a0002c0004 | 0/0 | 1302 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | ATGGC others(1297): Show |
chr13 | 21487691 | 21609170 | ||
| a0003c0007 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | ATGGC others(1297): Show |
chr13 | 21487691 | 21609170 | ||
| a0004c0009 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | ATGGC others(1297): Show |
chr13 | 21487691 | 21609170 | ||
| a0005c0005 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | ATGGC others(1297): Show |
chr13 | 21487691 | 21609170 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1885 | 122 | 24 | 24 | 51 | 6 | 17 | MICU2_chr13_21487691_21609170 | MICU2 | GCCTA others(1880): Show |
chr13 | 21487691 | 21609170 |
| a0001c0001t0002 | 0/0 | 1885 | 90 | 3 | 21 | 55 | 4 | 7 | MICU2_chr13_21487691_21609170 | MICU2 | GCGTA others(1880): Show |
chr13 | 21487691 | 21609170 |
| a0001c0001t0003 | 1/0 | 1885 | 33 | 26 | 6 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | GCCTA others(1880): Show |
chr13 | 21487691 | 21609170 |
| a0001c0001t0004 | 0/0 | 1885 | 14 | 11 | 2 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | GCCTA others(1880): Show |
chr13 | 21487691 | 21609170 |
| a0001c0001t0007 | 0/0 | 1885 | 4 | 2 | 0 | 0 | 0 | 2 | MICU2_chr13_21487691_21609170 | MICU2 | GCGTA others(1880): Show |
chr13 | 21487691 | 21609170 |
| a0001c0001t0008 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | GCCTA others(1880): Show |
chr13 | 21487691 | 21609170 |
| a0001c0001t0009 | 0/1 | 1885 | 1 | 0 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | GTGTA others(1880): Show |
chr13 | 21487691 | 21609170 |
| a0001c0002t0001 | 0/0 | 1885 | 10 | 10 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | GCCTA others(1880): Show |
chr13 | 21487691 | 21609170 |
| a0001c0002t0005 | 0/0 | 1885 | 8 | 7 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | GCCTA others(1880): Show |
chr13 | 21487691 | 21609170 |
| a0001c0002t0006 | 0/0 | 1885 | 5 | 4 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | GCCTA others(1880): Show |
chr13 | 21487691 | 21609170 |
| a0001c0003t0003 | 0/0 | 1885 | 22 | 2 | 8 | 0 | 6 | 6 | MICU2_chr13_21487691_21609170 | MICU2 | GCCTA others(1880): Show |
chr13 | 21487691 | 21609170 |
| a0001c0006t0005 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | GCCTA others(1880): Show |
chr13 | 21487691 | 21609170 |
| a0001c0008t0001 | 0/0 | 1885 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | GCCTA others(1880): Show |
chr13 | 21487691 | 21609170 |
| a0002c0004t0003 | 0/0 | 1885 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | GCCTA others(1880): Show |
chr13 | 21487691 | 21609170 |
| a0003c0007t0001 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | GCCTA others(1880): Show |
chr13 | 21487691 | 21609170 |
| a0004c0009t0001 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | GCCTA others(1880): Show |
chr13 | 21487691 | 21609170 |
| a0005c0005t0001 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | GCCTA others(1880): Show |
chr13 | 21487691 | 21609170 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0040 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0007g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0007g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0007g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0007g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0008g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0001t0009g0314 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0005g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0006g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0002t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0003t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0006t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0001c0008t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0002c0004t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0003c0007t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0004c0009t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| a0005c0005t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0238 | EUR | GBR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | GBR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | FIN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0256 | EUR | FIN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00323 | hp2 | a0001 | c0003 | t0003 | g0008 | EUR | FIN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | CHS | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | CHS | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0182 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | CHS | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | CHS | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0198 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00735 | hp2 | a0001 | c0002 | t0006 | g0028 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00738 | hp1 | a0001 | c0003 | t0003 | g0013 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01069 | hp2 | a0001 | c0003 | t0003 | g0016 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01070 | hp1 | a0002 | c0004 | t0003 | g0006 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01071 | hp1 | a0001 | c0003 | t0003 | g0015 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0194 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0212 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01106 | hp2 | a0001 | c0003 | t0003 | g0022 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0136 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01192 | hp2 | a0001 | c0002 | t0005 | g0217 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | CLM | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | CLM | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | CLM | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01358 | hp1 | a0001 | c0003 | t0003 | g0012 | AMR | CLM | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0138 | AMR | CLM | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | CLM | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01433 | hp1 | a0001 | c0003 | t0003 | g0004 | AMR | CLM | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | IBS | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0258 | EUR | IBS | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01516 | hp1 | a0001 | c0003 | t0003 | g0020 | EUR | IBS | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01517 | hp1 | a0001 | c0003 | t0003 | g0019 | EUR | IBS | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0257 | EUR | IBS | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01884 | hp2 | a0001 | c0003 | t0003 | g0014 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PEL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PEL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | PEL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01981 | hp2 | a0001 | c0003 | t0003 | g0017 | AMR | PEL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | KHV | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | KHV | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0184 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | KHV | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | KHV | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | KHV | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | KHV | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CDX | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | CDX | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | CDX | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02258 | hp1 | a0003 | c0007 | t0001 | g0219 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0313 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02602 | hp1 | a0001 | c0003 | t0003 | g0010 | SAS | PJL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02622 | hp1 | a0001 | c0002 | t0006 | g0128 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0199 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0144 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02723 | hp1 | a0001 | c0002 | t0005 | g0209 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0309 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0310 | SAS | PJL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02738 | hp2 | a0001 | c0003 | t0003 | g0018 | SAS | PJL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02886 | hp1 | a0001 | c0002 | t0005 | g0211 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02886 | hp2 | a0004 | c0009 | t0001 | g0173 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | ESN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | ESN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0188 | AFR | ESN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | ESN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02976 | hp2 | a0001 | c0002 | t0006 | g0127 | AFR | ESN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03017 | hp2 | a0001 | c0008 | t0001 | g0057 | SAS | PJL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03098 | hp2 | a0001 | c0002 | t0005 | g0213 | AFR | MSL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | ESN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03130 | hp2 | a0005 | c0005 | t0001 | g0026 | AFR | ESN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | ESN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0185 | AFR | ESN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | ESN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | MSL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | MSL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03225 | hp2 | a0001 | c0002 | t0006 | g0181 | AFR | MSL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | MSL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | PJL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0189 | AFR | ESN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | ESN | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0308 | AFR | GWD | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03579 | hp1 | a0001 | c0002 | t0005 | g0215 | AFR | MSL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | MSL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03704 | hp1 | a0001 | c0003 | t0003 | g0024 | SAS | PJL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | BEB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | BEB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03927 | hp2 | a0001 | c0003 | t0003 | g0023 | SAS | BEB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0299 | SAS | BEB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG04115 | hp1 | a0001 | c0001 | t0007 | g0306 | SAS | STU | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0220 | SAS | STU | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0200 | SAS | STU | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG04204 | hp1 | a0001 | c0003 | t0003 | g0025 | SAS | STU | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | STU | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | YRI | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | YRI | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | CHB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | YRI | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18906 | hp2 | a0001 | c0002 | t0005 | g0216 | AFR | YRI | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | LWK | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | LWK | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | LWK | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | YRI | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | YRI | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ASW | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | ASW | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA20752 | hp1 | a0001 | c0003 | t0003 | g0009 | EUR | TSI | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | TSI | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA20805 | hp1 | a0001 | c0003 | t0003 | g0011 | EUR | TSI | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA20805 | hp2 | a0001 | c0003 | t0003 | g0003 | EUR | TSI | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA20905 | hp1 | a0001 | c0003 | t0003 | g0021 | SAS | GIH | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0307 | SAS | GIH | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | CLM | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG01123 | hp2 | a0001 | c0003 | t0003 | g0005 | AMR | CLM | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02486 | hp1 | a0001 | c0003 | t0003 | g0007 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0179 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02559 | hp1 | a0001 | c0002 | t0005 | g0218 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03471 | hp1 | a0001 | c0006 | t0005 | g0214 | AFR | MSL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0130 | AFR | MSL | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | USA | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| HG06807 | hp2 | a0001 | c0002 | t0006 | g0190 | AFR | USA | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | USA | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0180 | AFR | USA | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| NA21309 | hp2 | a0001 | c0002 | t0005 | g0210 | AFR | LWK | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0009 | g0314 | REF | REF | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0040 | REF | REF | MICU2_chr13_21487691_21609170 | MICU2 | chr13 | 21487691 | 21609170 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:21496097 | T | C | 1 | a0004 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.997A>G | p.Ile333Val | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 10/12 | 1019/1885 | 997/1305 | 333/434 | chr13 | 21496097 | |||
| chr13:21502942 | T | A | 1 | a0002 | 1 | HG01070.hp1 | missense_variant | MODERATE | c.917A>T | p.Lys306Met | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/12 | 939/1885 | 917/1305 | 306/434 | chr13 | 21502942 | |||
| chr13:21502943 | T | A | 1 | a0002 | 1 | HG01070.hp1 | stop_gained | HIGH | c.916A>T | p.Lys306* | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/12 | 938/1885 | 916/1305 | 306/434 | chr13 | 21502943 | |||
| chr13:21503087 | T | C | 1 | a0003 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.772A>G | p.Asn258Asp | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/12 | 794/1885 | 772/1305 | 258/434 | chr13 | 21503087 | |||
| chr13:21604010 | C | G | 1 | a0005 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.139G>C | p.Ala47Pro | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/12 | 161/1885 | 139/1305 | 47/434 | chr13 | 21604010 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:21493300 | G | A | 1 | a0001c0006 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.1254C>T | p.Ser418Ser | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 12/12 | 1276/1885 | 1254/1305 | 418/434 | chr13 | 21493300 | |||
| chr13:21495317 | C | T | 1 | a0001c0008 | 1 | HG03017.hp2 | splice_region_variant&synonymous_variant | LOW | c.1044G>A | p.Ala348Ala | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/12 | 1066/1885 | 1044/1305 | 348/434 | chr13 | 21495317 | |||
| chr13:21514388 | A | G | 3 | a0001c0002 a0001c0006 a0003c0007 |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
synonymous_variant | LOW | c.628T>C | p.Leu210Leu | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/12 | 650/1885 | 628/1305 | 210/434 | chr13 | 21514388 | |||
| chr13:21604119 | C | T | 2 | a0001c0003 a0002c0004 |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
synonymous_variant | LOW | c.30G>A | p.Arg10Arg | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/12 | 52/1885 | 30/1305 | 10/434 | chr13 | 21604119 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:21492737 | T | C | 1 | a0001c0002t0006 | 5 | HG00735.hp2 HG02622.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*512A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 12/12 | 512 | chr13 | 21492737 | ||||||
| chr13:21492795 | G | A | 4 | a0001c0001t0002 a0001c0001t0004 a0001c0002t0005 others(1): Show |
113 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*454C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 12/12 | 454 | chr13 | 21492795 | ||||||
| chr13:21492921 | C | T | 1 | a0001c0001t0008 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*328G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 12/12 | 328 | chr13 | 21492921 | ||||||
| chr13:21492933 | T | C | 2 | a0001c0001t0002 a0001c0001t0004 |
104 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*316A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 12/12 | 316 | chr13 | 21492933 | ||||||
| chr13:21493097 | A | C | 11 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(8): Show |
155 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*152T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 12/12 | 152 | chr13 | 21493097 | ||||||
| chr13:21493172 | T | C | 1 | a0001c0002t0006 | 5 | HG00735.hp2 HG02622.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*77A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 12/12 | 77 | chr13 | 21493172 | ||||||
| chr13:21604168 | G | C | 2 | a0001c0001t0002 a0001c0001t0007 |
94 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(91): Show |
5_prime_UTR_variant | MODIFIER | c.-20C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/12 | 20 | chr13 | 21604168 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:21493358 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG03710.hp1 | splice_region_variant&intron_variant | LOW | c.1201-5A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21493358 | |||||||
| chr13:21493363 | G | A | 1 | a0001c0003t0003g0005 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1201-10C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21493363 | |||||||
| chr13:21493500 | G | C | 1 | a0001c0001t0004g0212 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1201-147C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21493500 | |||||||
| chr13:21493512 | G | A | 25 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1201-159C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21493512 | |||||||
| chr13:21493542 | T | C | 129 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(126): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1201-189A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21493542 | |||||||
| chr13:21493670 | A | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(216): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1201-317T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21493670 | |||||||
| chr13:21493686 | A | C | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1201-333T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21493686 | |||||||
| chr13:21493702 | TC | T | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1201-350delG | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21493702 | |||||||
| chr13:21493739 | A | C | 5 | a0001c0002t0006g0028 a0001c0002t0006g0127 a0001c0002t0006g0128 others(2): Show |
5 | HG00735.hp2 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201-386T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21493739 | |||||||
| chr13:21493784 | TAA | T | 13 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0032 others(10): Show |
13 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1201-433_1201-432d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21493784 | |||||||
| chr13:21493806 | G | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(308): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.1201-453C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21493806 | |||||||
| chr13:21493906 | T | G | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1201-553A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21493906 | |||||||
| chr13:21493996 | T | G | 25 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1201-643A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21493996 | |||||||
| chr13:21494086 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(134): Show |
139 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1201-733A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21494086 | |||||||
| chr13:21494137 | G | A | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1201-784C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21494137 | |||||||
| chr13:21494150 | T | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(294): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1201-797A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21494150 | |||||||
| chr13:21494157 | A | G | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1201-804T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21494157 | |||||||
| chr13:21494287 | T | C | 9 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+874A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21494287 | |||||||
| chr13:21494557 | T | G | 3 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 |
3 | HG01167.hp1 HG01169.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1200+604A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21494557 | |||||||
| chr13:21494774 | C | T | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1200+387G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21494774 | |||||||
| chr13:21494868 | T | A | 1 | a0001c0008t0001g0057 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1200+293A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21494868 | |||||||
| chr13:21494973 | C | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(285): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1200+188G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21494973 | |||||||
| chr13:21495012 | T | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG01516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1200+149A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21495012 | |||||||
| chr13:21495072 | CATTT | C | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1200+85_1200+88del others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21495072 | |||||||
| chr13:21495113 | T | A | 11 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(8): Show |
11 | HG00639.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1200+48A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21495113 | |||||||
| chr13:21495144 | TA | T | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1200+16delT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 11/11 | chr13 | 21495144 | |||||||
| chr13:21495575 | G | A | 1 | a0004c0009t0001g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1043-257C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 10/11 | chr13 | 21495575 | |||||||
| chr13:21495593 | T | C | 1 | a0001c0001t0003g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1043-275A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 10/11 | chr13 | 21495593 | |||||||
| chr13:21495599 | G | A | 1 | a0001c0001t0003g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1043-281C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 10/11 | chr13 | 21495599 | |||||||
| chr13:21495681 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(133): Show |
138 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.1043-363C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 10/11 | chr13 | 21495681 | |||||||
| chr13:21495830 | G | A | 3 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 |
3 | HG01167.hp1 HG01169.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1042+222C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 10/11 | chr13 | 21495830 | |||||||
| chr13:21495992 | A | G | 25 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1042+60T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 10/11 | chr13 | 21495992 | |||||||
| chr13:21496341 | G | A | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.934-181C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21496341 | |||||||
| chr13:21496483 | C | T | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(293): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.934-323G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21496483 | |||||||
| chr13:21496654 | T | G | 1 | a0001c0001t0007g0306 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.934-494A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21496654 | |||||||
| chr13:21496666 | G | A | 1 | a0001c0001t0002g0296 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.934-506C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21496666 | |||||||
| chr13:21496772 | T | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(294): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.934-612A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21496772 | |||||||
| chr13:21496790 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.934-630A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21496790 | |||||||
| chr13:21496796 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.934-636G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21496796 | |||||||
| chr13:21496830 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.934-670G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21496830 | |||||||
| chr13:21496838 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.934-678C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21496838 | |||||||
| chr13:21496844 | G | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(285): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.934-684C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21496844 | |||||||
| chr13:21496846 | A | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(285): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.934-686T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21496846 | |||||||
| chr13:21496918 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.934-758G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21496918 | |||||||
| chr13:21496919 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.934-759C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21496919 | |||||||
| chr13:21497048 | C | T | 1 | a0001c0002t0001g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.934-888G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21497048 | |||||||
| chr13:21497162 | C | G | 1 | a0001c0001t0003g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.934-1002G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21497162 | |||||||
| chr13:21497200 | G | GA | 12 | a0001c0001t0002g0300 a0001c0002t0001g0029 a0001c0002t0001g0030 others(9): Show |
12 | HG00673.hp2 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.934-1041dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21497200 | |||||||
| chr13:21497203 | A | G | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | HG02071.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.934-1043T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21497203 | |||||||
| chr13:21497319 | C | T | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.934-1159G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21497319 | |||||||
| chr13:21497362 | G | C | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.934-1202C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21497362 | |||||||
| chr13:21497559 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(84): Show |
89 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.934-1399T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21497559 | |||||||
| chr13:21497574 | G | A | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.934-1414C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21497574 | |||||||
| chr13:21497598 | G | A | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.934-1438C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21497598 | |||||||
| chr13:21497732 | T | C | 9 | a0001c0002t0005g0209 a0001c0002t0005g0210 a0001c0002t0005g0211 others(6): Show |
9 | HG01192.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.934-1572A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21497732 | |||||||
| chr13:21497740 | G | A | 1 | a0001c0002t0001g0029 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.934-1580C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21497740 | |||||||
| chr13:21497744 | G | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0064 others(4): Show |
8 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.934-1584C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21497744 | |||||||
| chr13:21497944 | G | A | 1 | a0001c0001t0002g0296 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.934-1784C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21497944 | |||||||
| chr13:21497952 | G | A | 1 | a0001c0006t0005g0214 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.934-1792C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21497952 | |||||||
| chr13:21498116 | G | C | 1 | a0001c0001t0002g0255 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.934-1956C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498116 | |||||||
| chr13:21498283 | G | A | 1 | a0001c0003t0003g0013 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.934-2123C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498283 | |||||||
| chr13:21498369 | C | CT | 76 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0002g0221 others(73): Show |
76 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.934-2210dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498369 | |||||||
| chr13:21498369 | C | CTT | 17 | a0001c0001t0002g0223 a0001c0001t0002g0231 a0001c0001t0002g0240 others(14): Show |
17 | HG00423.hp1 HG00735.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.934-2211_934-2210d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498369 | |||||||
| chr13:21498369 | CT | C | 53 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0064 others(50): Show |
53 | HG00639.hp2 HG01169.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.934-2210delA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498369 | |||||||
| chr13:21498369 | CTT | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(87): Show |
92 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.934-2211_934-2210d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498369 | |||||||
| chr13:21498369 | CTTTTTTT others(3): Show |
C | 1 | a0001c0003t0003g0025 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.934-2219_934-2210d others(12): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498369 | |||||||
| chr13:21498369 | CTTTTTTT others(4): Show |
C | 21 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(18): Show |
21 | HG00323.hp2 HG00738.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.934-2220_934-2210d others(13): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498369 | |||||||
| chr13:21498369 | CTTTTTTT others(5): Show |
C | 1 | a0001c0003t0003g0016 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.934-2221_934-2210d others(14): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498369 | |||||||
| chr13:21498369 | CTTTTTTT others(10): Show |
C | 7 | a0001c0001t0002g0312 a0001c0001t0003g0039 a0001c0001t0003g0129 others(4): Show |
7 | HG01069.hp1 HG01243.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.934-2226_934-2210d others(19): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498369 | |||||||
| chr13:21498431 | C | T | 9 | a0001c0002t0005g0209 a0001c0002t0005g0210 a0001c0002t0005g0211 others(6): Show |
9 | HG01192.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.934-2271G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498431 | |||||||
| chr13:21498626 | A | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(285): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.934-2466T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498626 | |||||||
| chr13:21498821 | G | GA | 111 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(108): Show |
111 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.934-2662dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498821 | |||||||
| chr13:21498821 | GA | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(86): Show |
91 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.934-2662delT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498821 | |||||||
| chr13:21498828 | A | G | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.934-2668T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498828 | |||||||
| chr13:21498855 | T | TAA | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.934-2697_934-2696d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498855 | |||||||
| chr13:21498864 | C | T | 1 | a0001c0002t0005g0218 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.934-2704G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498864 | |||||||
| chr13:21498872 | A | G | 9 | a0001c0002t0005g0209 a0001c0002t0005g0210 a0001c0002t0005g0211 others(6): Show |
9 | HG01192.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.934-2712T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498872 | |||||||
| chr13:21498897 | A | G | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(293): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.934-2737T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498897 | |||||||
| chr13:21498973 | C | T | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.934-2813G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21498973 | |||||||
| chr13:21499036 | C | T | 5 | a0001c0002t0006g0028 a0001c0002t0006g0127 a0001c0002t0006g0128 others(2): Show |
5 | HG00735.hp2 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.934-2876G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21499036 | |||||||
| chr13:21499049 | C | G | 1 | a0001c0001t0002g0294 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.934-2889G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21499049 | |||||||
| chr13:21499099 | C | T | 9 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0015 others(6): Show |
9 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.934-2939G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21499099 | |||||||
| chr13:21499192 | C | G | 46 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(43): Show |
46 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.934-3032G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21499192 | |||||||
| chr13:21499440 | C | T | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.934-3280G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21499440 | |||||||
| chr13:21499635 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.933+3291G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21499635 | |||||||
| chr13:21499656 | C | T | 1 | a0001c0002t0001g0034 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.933+3270G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21499656 | |||||||
| chr13:21499777 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.933+3149C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21499777 | |||||||
| chr13:21499835 | CCAA | C | 143 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(140): Show |
143 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.933+3088_933+3090d others(5): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21499835 | |||||||
| chr13:21499975 | C | G | 1 | a0001c0002t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.933+2951G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21499975 | |||||||
| chr13:21499987 | G | A | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.933+2939C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21499987 | |||||||
| chr13:21500046 | CTTGT | C | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.933+2876_933+2879d others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500046 | |||||||
| chr13:21500146 | AGCATCAT | A | 127 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(124): Show |
127 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.933+2773_933+2779d others(9): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500146 | |||||||
| chr13:21500225 | A | G | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.933+2701T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500225 | |||||||
| chr13:21500372 | G | A | 3 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 |
3 | HG01167.hp1 HG01169.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.933+2554C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500372 | |||||||
| chr13:21500417 | AT | A | 6 | a0001c0001t0002g0240 a0001c0001t0002g0243 a0001c0001t0002g0295 others(3): Show |
6 | HG02027.hp2 HG02486.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.933+2508delA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500417 | |||||||
| chr13:21500417 | ATT | A | 97 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(94): Show |
97 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.933+2507_933+2508d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500417 | |||||||
| chr13:21500417 | ATTT | A | 10 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0175 others(7): Show |
10 | HG01069.hp1 HG02258.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.933+2506_933+2508d others(5): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500417 | |||||||
| chr13:21500417 | ATTTT | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(115): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.933+2505_933+2508d others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500417 | |||||||
| chr13:21500417 | ATTTTT | A | 43 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0150 others(40): Show |
43 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.933+2504_933+2508d others(7): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500417 | |||||||
| chr13:21500417 | ATTTTTTT | A | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.933+2502_933+2508d others(9): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500417 | |||||||
| chr13:21500426 | T | G | 1 | a0001c0001t0002g0234 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.933+2500A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500426 | |||||||
| chr13:21500427 | T | G | 4 | a0001c0001t0002g0240 a0001c0001t0002g0243 a0001c0001t0002g0295 others(1): Show |
4 | HG02027.hp2 HG02738.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.933+2499A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500427 | |||||||
| chr13:21500428 | T | G | 81 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(78): Show |
81 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.933+2498A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500428 | |||||||
| chr13:21500429 | T | G | 2 | a0001c0001t0002g0227 a0001c0001t0003g0140 |
2 | HG02717.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.933+2497A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500429 | |||||||
| chr13:21500431 | T | G | 1 | a0001c0001t0002g0234 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.933+2495A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500431 | |||||||
| chr13:21500432 | T | G | 7 | a0001c0001t0002g0240 a0001c0001t0002g0243 a0001c0001t0002g0295 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.933+2494A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500432 | |||||||
| chr13:21500433 | T | C | 1 | a0001c0001t0002g0243 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.933+2493A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500433 | |||||||
| chr13:21500433 | T | G | 96 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0175 others(93): Show |
96 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.933+2493A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500433 | |||||||
| chr13:21500434 | T | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(158): Show |
163 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.933+2492A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500434 | |||||||
| chr13:21500435 | T | G | 6 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(3): Show |
6 | HG02735.hp2 HG03831.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.933+2491A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500435 | |||||||
| chr13:21500436 | T | G | 19 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(16): Show |
19 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.933+2490A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500436 | |||||||
| chr13:21500437 | T | G | 5 | a0001c0001t0001g0175 a0001c0001t0003g0135 a0001c0001t0003g0139 others(2): Show |
5 | HG02717.hp1 NA19030.hp2 NA20129.hp2 others(2): Show |
intron_variant | MODIFIER | c.933+2489A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500437 | |||||||
| chr13:21500592 | AT | A | 4 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0037 others(1): Show |
4 | HG02572.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.933+2333delA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500592 | |||||||
| chr13:21500740 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.933+2186T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500740 | |||||||
| chr13:21500941 | T | C | 22 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(19): Show |
22 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.933+1985A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21500941 | |||||||
| chr13:21501004 | C | G | 86 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(83): Show |
86 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.933+1922G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501004 | |||||||
| chr13:21501192 | T | G | 1 | a0001c0001t0002g0251 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.933+1734A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501192 | |||||||
| chr13:21501222 | G | T | 1 | a0001c0001t0002g0284 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.933+1704C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501222 | |||||||
| chr13:21501268 | C | CT | 25 | a0001c0001t0002g0310 a0001c0002t0001g0029 a0001c0002t0001g0030 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.933+1657dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501268 | |||||||
| chr13:21501325 | C | T | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.933+1601G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501325 | |||||||
| chr13:21501341 | A | C | 1 | a0001c0001t0002g0238 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.933+1585T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501341 | |||||||
| chr13:21501387 | C | T | 5 | a0001c0002t0006g0028 a0001c0002t0006g0127 a0001c0002t0006g0128 others(2): Show |
5 | HG00735.hp2 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.933+1539G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501387 | |||||||
| chr13:21501408 | A | G | 125 | a0001c0001t0001g0090 a0001c0001t0001g0121 a0001c0001t0001g0156 others(122): Show |
125 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.933+1518T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501408 | |||||||
| chr13:21501453 | G | A | 16 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(13): Show |
16 | HG00738.hp2 HG01106.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.933+1473C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501453 | |||||||
| chr13:21501454 | T | G | 20 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0151 others(17): Show |
20 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.933+1472A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501454 | |||||||
| chr13:21501470 | A | G | 23 | a0001c0001t0002g0236 a0001c0001t0002g0238 a0001c0001t0002g0252 others(20): Show |
23 | HG00140.hp1 HG01081.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.933+1456T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501470 | |||||||
| chr13:21501480 | T | C | 1 | a0001c0001t0002g0274 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.933+1446A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501480 | |||||||
| chr13:21501483 | T | C | 2 | a0001c0001t0002g0285 a0001c0001t0002g0291 |
2 | HG00423.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.933+1443A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501483 | |||||||
| chr13:21501496 | T | G | 1 | a0001c0001t0004g0185 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.933+1430A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501496 | |||||||
| chr13:21501498 | A | G | 18 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(15): Show |
18 | HG01891.hp1 HG02055.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.933+1428T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501498 | |||||||
| chr13:21501504 | T | C | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.933+1422A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501504 | |||||||
| chr13:21501513 | T | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0064 others(15): Show |
19 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.933+1413A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501513 | |||||||
| chr13:21501657 | C | T | 1 | a0001c0003t0003g0017 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.933+1269G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501657 | |||||||
| chr13:21501868 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(287): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.933+1058A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501868 | |||||||
| chr13:21501952 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(134): Show |
139 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.933+974A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501952 | |||||||
| chr13:21501990 | A | T | 1 | a0001c0001t0002g0294 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.933+936T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21501990 | |||||||
| chr13:21502120 | T | C | 25 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.933+806A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21502120 | |||||||
| chr13:21502144 | TTTC | T | 104 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(101): Show |
104 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.933+779_933+781del others(3): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21502144 | |||||||
| chr13:21502228 | T | TTATC | 25 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.933+697_933+698ins others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21502228 | |||||||
| chr13:21502352 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(84): Show |
89 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.933+574G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21502352 | |||||||
| chr13:21502361 | A | C | 25 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.933+565T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21502361 | |||||||
| chr13:21502502 | G | C | 2 | a0001c0001t0003g0136 a0001c0001t0003g0137 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.933+424C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21502502 | |||||||
| chr13:21502502 | G | T | 25 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.933+424C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21502502 | |||||||
| chr13:21502600 | A | G | 25 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.933+326T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21502600 | |||||||
| chr13:21502690 | T | C | 22 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(19): Show |
22 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.933+236A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21502690 | |||||||
| chr13:21502761 | C | CAGT | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(294): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.933+162_933+164dup others(3): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21502761 | |||||||
| chr13:21502791 | G | C | 104 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(101): Show |
104 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.933+135C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 9/11 | chr13 | 21502791 | |||||||
| chr13:21503134 | T | C | 1 | a0001c0001t0002g0284 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.762-37A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21503134 | |||||||
| chr13:21503305 | A | C | 1 | a0001c0001t0002g0299 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.762-208T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21503305 | |||||||
| chr13:21503424 | T | G | 1 | a0001c0001t0002g0292 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.762-327A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21503424 | |||||||
| chr13:21503468 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.762-371C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21503468 | |||||||
| chr13:21503529 | T | C | 1 | a0001c0001t0004g0141 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.762-432A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21503529 | |||||||
| chr13:21503585 | C | T | 1 | a0001c0001t0008g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.762-488G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21503585 | |||||||
| chr13:21503800 | G | A | 1 | a0001c0001t0003g0192 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.762-703C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21503800 | |||||||
| chr13:21503975 | G | T | 1 | a0005c0005t0001g0026 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.762-878C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21503975 | |||||||
| chr13:21504035 | T | C | 22 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(19): Show |
22 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.762-938A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21504035 | |||||||
| chr13:21504274 | C | T | 104 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(101): Show |
104 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.762-1177G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21504274 | |||||||
| chr13:21504347 | C | T | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(285): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.762-1250G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21504347 | |||||||
| chr13:21504383 | T | C | 1 | a0001c0001t0004g0141 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.762-1286A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21504383 | |||||||
| chr13:21504398 | C | T | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.762-1301G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21504398 | |||||||
| chr13:21504423 | T | G | 9 | a0001c0002t0005g0209 a0001c0002t0005g0210 a0001c0002t0005g0211 others(6): Show |
9 | HG01192.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.762-1326A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21504423 | |||||||
| chr13:21504513 | A | C | 5 | a0001c0002t0006g0028 a0001c0002t0006g0127 a0001c0002t0006g0128 others(2): Show |
5 | HG00735.hp2 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.762-1416T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21504513 | |||||||
| chr13:21504576 | C | G | 5 | a0001c0002t0006g0028 a0001c0002t0006g0127 a0001c0002t0006g0128 others(2): Show |
5 | HG00735.hp2 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.762-1479G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21504576 | |||||||
| chr13:21504717 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.762-1620A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21504717 | |||||||
| chr13:21504752 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.762-1655C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21504752 | |||||||
| chr13:21504957 | C | T | 9 | a0001c0002t0005g0209 a0001c0002t0005g0210 a0001c0002t0005g0211 others(6): Show |
9 | HG01192.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.762-1860G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21504957 | |||||||
| chr13:21505015 | A | T | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(293): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.762-1918T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21505015 | |||||||
| chr13:21505197 | G | C | 1 | a0001c0001t0002g0251 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.762-2100C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21505197 | |||||||
| chr13:21505240 | A | T | 3 | a0001c0002t0006g0028 a0001c0002t0006g0181 a0001c0002t0006g0190 |
3 | HG00735.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.762-2143T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21505240 | |||||||
| chr13:21505308 | A | C | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.762-2211T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21505308 | |||||||
| chr13:21505451 | A | C | 5 | a0001c0002t0006g0028 a0001c0002t0006g0127 a0001c0002t0006g0128 others(2): Show |
5 | HG00735.hp2 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.762-2354T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21505451 | |||||||
| chr13:21505468 | A | G | 9 | a0001c0002t0005g0209 a0001c0002t0005g0210 a0001c0002t0005g0211 others(6): Show |
9 | HG01192.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.762-2371T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21505468 | |||||||
| chr13:21505519 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.762-2422A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21505519 | |||||||
| chr13:21505529 | T | C | 3 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0142 |
3 | HG02717.hp1 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.762-2432A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21505529 | |||||||
| chr13:21505621 | T | C | 1 | a0001c0001t0002g0297 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.762-2524A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21505621 | |||||||
| chr13:21505644 | C | T | 5 | a0001c0002t0006g0028 a0001c0002t0006g0127 a0001c0002t0006g0128 others(2): Show |
5 | HG00735.hp2 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.762-2547G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21505644 | |||||||
| chr13:21505796 | G | A | 1 | a0001c0001t0002g0294 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.762-2699C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21505796 | |||||||
| chr13:21505856 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.762-2759T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21505856 | |||||||
| chr13:21505866 | A | G | 2 | a0001c0001t0003g0174 a0001c0001t0003g0177 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.762-2769T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21505866 | |||||||
| chr13:21505960 | T | C | 25 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.762-2863A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21505960 | |||||||
| chr13:21506018 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.762-2921G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21506018 | |||||||
| chr13:21506074 | G | C | 3 | a0001c0001t0003g0174 a0001c0001t0003g0177 a0001c0001t0008g0144 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.762-2977C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21506074 | |||||||
| chr13:21506143 | C | T | 2 | a0001c0001t0004g0182 a0001c0001t0004g0183 |
2 | HG00639.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.762-3046G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21506143 | |||||||
| chr13:21506168 | A | G | 25 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.762-3071T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21506168 | |||||||
| chr13:21506246 | A | G | 25 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.762-3149T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21506246 | |||||||
| chr13:21506307 | C | T | 1 | a0001c0001t0008g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.762-3210G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21506307 | |||||||
| chr13:21506386 | T | C | 1 | a0001c0003t0003g0003 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.762-3289A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21506386 | |||||||
| chr13:21506597 | T | C | 25 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.761+3407A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21506597 | |||||||
| chr13:21506797 | C | T | 5 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
5 | HG01175.hp2 HG02735.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.761+3207G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21506797 | |||||||
| chr13:21506933 | T | C | 1 | a0001c0002t0006g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.761+3071A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21506933 | |||||||
| chr13:21507167 | A | G | 25 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.761+2837T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21507167 | |||||||
| chr13:21507238 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(86): Show |
91 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.761+2766T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21507238 | |||||||
| chr13:21507332 | A | G | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(300): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.761+2672T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21507332 | |||||||
| chr13:21507359 | T | A | 1 | a0001c0001t0001g0159 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.761+2645A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21507359 | |||||||
| chr13:21507606 | A | AT | 31 | a0001c0001t0001g0116 a0001c0001t0001g0148 a0001c0001t0002g0234 others(28): Show |
31 | HG00735.hp2 HG01192.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.761+2397dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21507606 | |||||||
| chr13:21507607 | T | A | 21 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(18): Show |
21 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.761+2397A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21507607 | |||||||
| chr13:21507697 | G | A | 104 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(101): Show |
104 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.761+2307C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21507697 | |||||||
| chr13:21507760 | C | T | 9 | a0001c0002t0005g0209 a0001c0002t0005g0210 a0001c0002t0005g0211 others(6): Show |
9 | HG01192.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.761+2244G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21507760 | |||||||
| chr13:21507764 | C | T | 2 | a0001c0001t0002g0239 a0001c0001t0003g0027 |
2 | HG02818.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.761+2240G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21507764 | |||||||
| chr13:21507765 | G | A | 9 | a0001c0002t0005g0209 a0001c0002t0005g0210 a0001c0002t0005g0211 others(6): Show |
9 | HG01192.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.761+2239C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21507765 | |||||||
| chr13:21507894 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0064 a0001c0001t0001g0074 others(1): Show |
4 | HG02735.hp1 HG03017.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.761+2110C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21507894 | |||||||
| chr13:21507952 | A | G | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.761+2052T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21507952 | |||||||
| chr13:21508017 | G | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0064 a0001c0001t0001g0074 others(1): Show |
4 | HG02735.hp1 HG03017.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.761+1987C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21508017 | |||||||
| chr13:21508107 | A | C | 5 | a0001c0002t0006g0028 a0001c0002t0006g0127 a0001c0002t0006g0128 others(2): Show |
5 | HG00735.hp2 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.761+1897T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21508107 | |||||||
| chr13:21508128 | C | CT | 37 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0111 others(34): Show |
37 | HG00735.hp2 HG01192.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.761+1875dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21508128 | |||||||
| chr13:21508212 | G | A | 1 | a0001c0003t0003g0025 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.761+1792C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21508212 | |||||||
| chr13:21508238 | G | A | 5 | a0001c0002t0006g0028 a0001c0002t0006g0127 a0001c0002t0006g0128 others(2): Show |
5 | HG00735.hp2 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.761+1766C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21508238 | |||||||
| chr13:21508274 | T | C | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.761+1730A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21508274 | |||||||
| chr13:21508389 | G | A | 1 | a0001c0001t0004g0141 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.761+1615C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21508389 | |||||||
| chr13:21508435 | T | C | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.761+1569A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21508435 | |||||||
| chr13:21508622 | T | A | 2 | a0001c0002t0001g0029 a0001c0002t0001g0035 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.761+1382A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21508622 | |||||||
| chr13:21508791 | A | G | 33 | a0001c0001t0003g0044 a0001c0001t0004g0178 a0001c0001t0004g0179 others(30): Show |
33 | HG01099.hp2 HG01192.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.761+1213T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21508791 | |||||||
| chr13:21508821 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.761+1183A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21508821 | |||||||
| chr13:21508925 | T | G | 46 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(43): Show |
46 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.761+1079A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21508925 | |||||||
| chr13:21509056 | C | G | 1 | a0004c0009t0001g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.761+948G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21509056 | |||||||
| chr13:21509194 | T | C | 6 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(3): Show |
6 | HG00323.hp2 HG01358.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.761+810A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21509194 | |||||||
| chr13:21509207 | G | A | 103 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(100): Show |
103 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.761+797C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21509207 | |||||||
| chr13:21509562 | A | AC | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.761+441dupG | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21509562 | |||||||
| chr13:21509698 | C | T | 5 | a0001c0002t0006g0028 a0001c0002t0006g0127 a0001c0002t0006g0128 others(2): Show |
5 | HG00735.hp2 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.761+306G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21509698 | |||||||
| chr13:21509723 | C | T | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.761+281G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21509723 | |||||||
| chr13:21509727 | T | G | 1 | a0001c0002t0001g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.761+277A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21509727 | |||||||
| chr13:21509788 | C | T | 9 | a0001c0002t0005g0209 a0001c0002t0005g0210 a0001c0002t0005g0211 others(6): Show |
9 | HG01192.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.761+216G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21509788 | |||||||
| chr13:21509859 | A | C | 128 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(125): Show |
128 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.761+145T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21509859 | |||||||
| chr13:21509927 | G | C | 1 | a0001c0001t0001g0153 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.761+77C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21509927 | |||||||
| chr13:21509940 | TTC | T | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.761+62_761+63delGA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 8/11 | chr13 | 21509940 | |||||||
| chr13:21510360 | G | C | 129 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(126): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.664-259C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21510360 | |||||||
| chr13:21510793 | GCCTTAGG others(54): Show |
G | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.664-753_664-693del others(61): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21510793 | |||||||
| chr13:21510813 | A | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(257): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.664-712T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21510813 | |||||||
| chr13:21510856 | CTTAGGAG others(7): Show |
C | 16 | a0001c0001t0001g0175 a0001c0001t0003g0136 a0001c0001t0003g0137 others(13): Show |
16 | HG01070.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.664-769_664-756del others(14): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21510856 | |||||||
| chr13:21510870 | A | C | 2 | a0001c0001t0003g0135 a0001c0001t0003g0138 |
2 | HG01361.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.664-769T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21510870 | |||||||
| chr13:21511120 | G | C | 1 | a0001c0003t0003g0013 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.664-1019C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21511120 | |||||||
| chr13:21511501 | C | A | 9 | a0001c0002t0005g0209 a0001c0002t0005g0210 a0001c0002t0005g0211 others(6): Show |
9 | HG01192.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.664-1400G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21511501 | |||||||
| chr13:21511520 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(86): Show |
91 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.664-1419T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21511520 | |||||||
| chr13:21511718 | GACA | G | 46 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(43): Show |
46 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.664-1620_664-1618d others(5): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21511718 | |||||||
| chr13:21511795 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.664-1694A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21511795 | |||||||
| chr13:21511813 | AT | A | 10 | a0001c0001t0001g0090 a0001c0002t0006g0028 a0001c0002t0006g0127 others(7): Show |
10 | HG00735.hp2 HG01106.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.664-1713delA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21511813 | |||||||
| chr13:21511826 | T | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(87): Show |
92 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.664-1725A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21511826 | |||||||
| chr13:21511875 | A | G | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.664-1774T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21511875 | |||||||
| chr13:21511941 | A | G | 25 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.664-1840T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21511941 | |||||||
| chr13:21511988 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(148): Show |
153 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.664-1887T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21511988 | |||||||
| chr13:21512120 | C | T | 9 | a0001c0002t0005g0209 a0001c0002t0005g0210 a0001c0002t0005g0211 others(6): Show |
9 | HG01192.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.664-2019G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21512120 | |||||||
| chr13:21512169 | C | G | 1 | a0001c0001t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.664-2068G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21512169 | |||||||
| chr13:21512287 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.663+2066T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21512287 | |||||||
| chr13:21512443 | T | A | 1 | a0001c0001t0002g0224 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.663+1910A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21512443 | |||||||
| chr13:21512445 | A | AT | 110 | a0001c0001t0001g0164 a0001c0001t0001g0203 a0001c0001t0001g0207 others(107): Show |
110 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.663+1907dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21512445 | |||||||
| chr13:21512445 | A | T | 1 | a0001c0001t0002g0224 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.663+1908T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21512445 | |||||||
| chr13:21512445 | ATTTTTTT others(4): Show |
A | 9 | a0001c0002t0005g0209 a0001c0002t0005g0210 a0001c0002t0005g0211 others(6): Show |
9 | HG01192.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.663+1897_663+1907d others(13): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21512445 | |||||||
| chr13:21512479 | G | A | 45 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(42): Show |
45 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.663+1874C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21512479 | |||||||
| chr13:21512571 | C | T | 1 | a0001c0003t0003g0013 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.663+1782G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21512571 | |||||||
| chr13:21512716 | C | T | 5 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
5 | HG01175.hp2 HG02735.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.663+1637G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21512716 | |||||||
| chr13:21512740 | C | T | 1 | a0001c0001t0002g0236 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.663+1613G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21512740 | |||||||
| chr13:21512930 | A | G | 1 | a0001c0001t0002g0283 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.663+1423T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21512930 | |||||||
| chr13:21513047 | CAT | C | 9 | a0001c0002t0005g0209 a0001c0002t0005g0210 a0001c0002t0005g0211 others(6): Show |
9 | HG01192.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.663+1304_663+1305d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21513047 | |||||||
| chr13:21513056 | T | G | 5 | a0001c0002t0006g0028 a0001c0002t0006g0127 a0001c0002t0006g0128 others(2): Show |
5 | HG00735.hp2 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.663+1297A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21513056 | |||||||
| chr13:21513221 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.663+1132A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21513221 | |||||||
| chr13:21513279 | T | C | 1 | a0001c0001t0002g0273 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.663+1074A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21513279 | |||||||
| chr13:21513290 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.663+1063A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21513290 | |||||||
| chr13:21513424 | T | G | 1 | a0001c0001t0004g0183 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.663+929A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21513424 | |||||||
| chr13:21513454 | C | T | 1 | a0001c0003t0003g0025 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.663+899G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21513454 | |||||||
| chr13:21513467 | G | C | 46 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(43): Show |
46 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.663+886C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21513467 | |||||||
| chr13:21513595 | GGT | G | 9 | a0001c0002t0005g0209 a0001c0002t0005g0210 a0001c0002t0005g0211 others(6): Show |
9 | HG01192.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.663+756_663+757del others(2): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21513595 | |||||||
| chr13:21513696 | C | T | 9 | a0001c0002t0005g0209 a0001c0002t0005g0210 a0001c0002t0005g0211 others(6): Show |
9 | HG01192.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.663+657G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21513696 | |||||||
| chr13:21513739 | C | CA | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(117): Show |
122 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.663+613dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21513739 | |||||||
| chr13:21513739 | C | CAA | 50 | a0001c0001t0001g0049 a0001c0001t0001g0068 a0001c0001t0001g0078 others(47): Show |
50 | HG00639.hp2 HG01069.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.663+612_663+613dup others(2): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21513739 | |||||||
| chr13:21513739 | C | CAAA | 12 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0167 others(9): Show |
12 | HG01099.hp2 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.663+611_663+613dup others(3): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21513739 | |||||||
| chr13:21513739 | C | CAAAA | 62 | a0001c0001t0001g0166 a0001c0001t0002g0222 a0001c0001t0002g0224 others(59): Show |
62 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.663+610_663+613dup others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21513739 | |||||||
| chr13:21513739 | C | CAAAAA | 29 | a0001c0001t0002g0221 a0001c0001t0002g0223 a0001c0001t0002g0225 others(26): Show |
29 | HG00423.hp1 HG00673.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.663+609_663+613dup others(5): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21513739 | |||||||
| chr13:21513739 | CA | C | 8 | a0001c0002t0005g0209 a0001c0002t0005g0210 a0001c0002t0005g0211 others(5): Show |
8 | HG01192.hp2 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.663+613delT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21513739 | |||||||
| chr13:21514062 | T | C | 94 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(91): Show |
94 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.663+291A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21514062 | |||||||
| chr13:21514067 | G | T | 5 | a0001c0002t0006g0028 a0001c0002t0006g0127 a0001c0002t0006g0128 others(2): Show |
5 | HG00735.hp2 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.663+286C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21514067 | |||||||
| chr13:21514079 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.663+274C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21514079 | |||||||
| chr13:21514222 | G | A | 94 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(91): Show |
94 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.663+131C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 7/11 | chr13 | 21514222 | |||||||
| chr13:21514446 | A | G | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.598-28T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21514446 | |||||||
| chr13:21514449 | T | A | 2 | a0001c0001t0003g0174 a0001c0001t0003g0177 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.598-31A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21514449 | |||||||
| chr13:21514538 | T | A | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.598-120A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21514538 | |||||||
| chr13:21514540 | CT | C | 25 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.598-123delA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21514540 | |||||||
| chr13:21514551 | T | G | 25 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.598-133A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21514551 | |||||||
| chr13:21514594 | C | T | 94 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(91): Show |
94 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.598-176G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21514594 | |||||||
| chr13:21514683 | C | T | 46 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(43): Show |
46 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.598-265G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21514683 | |||||||
| chr13:21514698 | A | AT | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-281dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21514698 | |||||||
| chr13:21514698 | AT | A | 92 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0169 others(89): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.598-281delA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21514698 | |||||||
| chr13:21514741 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.598-323G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21514741 | |||||||
| chr13:21515064 | G | A | 1 | a0001c0001t0002g0285 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.598-646C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21515064 | |||||||
| chr13:21515085 | G | GTTTTT | 58 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(55): Show |
58 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.598-672_598-668dup others(5): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21515085 | |||||||
| chr13:21515085 | GT | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(217): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.598-668delA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21515085 | |||||||
| chr13:21515105 | G | A | 63 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(60): Show |
63 | HG00639.hp1 HG00673.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.598-687C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21515105 | |||||||
| chr13:21515175 | G | A | 4 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(1): Show |
4 | HG01106.hp2 HG03704.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.598-757C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21515175 | |||||||
| chr13:21515183 | G | A | 1 | a0001c0001t0002g0296 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.598-765C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21515183 | |||||||
| chr13:21515227 | A | G | 1 | a0001c0003t0003g0025 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.598-809T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21515227 | |||||||
| chr13:21515377 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0114 |
2 | HG02602.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.598-959G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21515377 | |||||||
| chr13:21515600 | A | T | 1 | a0001c0001t0002g0224 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.598-1182T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21515600 | |||||||
| chr13:21515750 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.598-1332G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21515750 | |||||||
| chr13:21515810 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(268): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.598-1392C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21515810 | |||||||
| chr13:21515822 | C | A | 9 | a0001c0002t0005g0209 a0001c0002t0005g0210 a0001c0002t0005g0211 others(6): Show |
9 | HG01192.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-1404G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21515822 | |||||||
| chr13:21515830 | A | G | 33 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(30): Show |
33 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.598-1412T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21515830 | |||||||
| chr13:21515861 | A | G | 7 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.598-1443T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21515861 | |||||||
| chr13:21515927 | A | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(96): Show |
101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.598-1509T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21515927 | |||||||
| chr13:21515937 | C | T | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.598-1519G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21515937 | |||||||
| chr13:21515960 | T | G | 1 | a0001c0001t0004g0187 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.598-1542A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21515960 | |||||||
| chr13:21516168 | T | C | 105 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(102): Show |
105 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.598-1750A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21516168 | |||||||
| chr13:21516227 | T | C | 1 | a0001c0001t0002g0286 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.598-1809A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21516227 | |||||||
| chr13:21516353 | C | T | 1 | a0001c0001t0002g0302 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.598-1935G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21516353 | |||||||
| chr13:21516486 | C | T | 1 | a0001c0001t0003g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.598-2068G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21516486 | |||||||
| chr13:21516591 | C | T | 2 | a0001c0001t0002g0247 a0001c0001t0002g0288 |
2 | HG02080.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.598-2173G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21516591 | |||||||
| chr13:21516608 | A | G | 1 | a0001c0001t0002g0243 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.598-2190T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21516608 | |||||||
| chr13:21516621 | A | G | 11 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(8): Show |
11 | HG00639.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.598-2203T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21516621 | |||||||
| chr13:21516687 | C | T | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.598-2269G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21516687 | |||||||
| chr13:21516692 | T | G | 7 | a0001c0001t0002g0237 a0001c0001t0002g0262 a0001c0001t0002g0275 others(4): Show |
7 | HG01255.hp2 HG01433.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.598-2274A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21516692 | |||||||
| chr13:21516905 | G | C | 1 | a0001c0001t0003g0192 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.598-2487C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21516905 | |||||||
| chr13:21516905 | G | T | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.598-2487C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21516905 | |||||||
| chr13:21516961 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.598-2543G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21516961 | |||||||
| chr13:21517014 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(142): Show |
147 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.598-2596T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517014 | |||||||
| chr13:21517085 | C | A | 1 | a0001c0003t0003g0011 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.598-2667G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517085 | |||||||
| chr13:21517175 | T | C | 1 | a0001c0001t0003g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.598-2757A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517175 | |||||||
| chr13:21517238 | A | G | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.598-2820T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517238 | |||||||
| chr13:21517257 | T | C | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.598-2839A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517257 | |||||||
| chr13:21517313 | T | C | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-2895A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517313 | |||||||
| chr13:21517329 | A | T | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(13): Show |
16 | HG00735.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.598-2911T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517329 | |||||||
| chr13:21517766 | C | T | 2 | a0001c0001t0002g0259 a0001c0001t0002g0294 |
2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.598-3348G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517766 | |||||||
| chr13:21517770 | G | GACACACA others(7): Show |
1 | a0001c0002t0006g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.598-3366_598-3353d others(16): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517770 | |||||||
| chr13:21517770 | GAC | G | 15 | a0001c0001t0003g0041 a0001c0001t0003g0043 a0001c0001t0003g0046 others(12): Show |
15 | HG00735.hp1 HG01074.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.598-3354_598-3353d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517770 | |||||||
| chr13:21517791 | A | G | 1 | a0001c0001t0004g0180 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.598-3373T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517791 | |||||||
| chr13:21517793 | A | ACG | 3 | a0001c0001t0004g0185 a0001c0001t0004g0187 a0001c0001t0004g0188 |
3 | HG02922.hp1 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.598-3376_598-3375i others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517793 | |||||||
| chr13:21517793 | A | G | 3 | a0001c0001t0004g0179 a0001c0001t0004g0180 a0001c0001t0004g0184 |
3 | HG02055.hp1 HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.598-3375T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517793 | |||||||
| chr13:21517793 | ACACACAC others(3): Show |
A | 1 | a0004c0009t0001g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.598-3385_598-3376d others(12): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517793 | |||||||
| chr13:21517795 | A | ACG | 5 | a0001c0001t0002g0250 a0001c0001t0004g0212 a0001c0003t0003g0010 others(2): Show |
5 | HG00738.hp1 HG01099.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-3378_598-3377i others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517795 | |||||||
| chr13:21517795 | A | G | 9 | a0001c0001t0003g0133 a0001c0001t0004g0179 a0001c0001t0004g0180 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.598-3377T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517795 | |||||||
| chr13:21517795 | ACACACGC others(1): Show |
A | 37 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(34): Show |
37 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.598-3385_598-3378d others(10): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517795 | |||||||
| chr13:21517795 | ACACACGC others(3): Show |
A | 1 | a0001c0001t0002g0283 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.598-3387_598-3378d others(12): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517795 | |||||||
| chr13:21517797 | A | ACG | 32 | a0001c0001t0002g0223 a0001c0001t0002g0226 a0001c0001t0002g0228 others(29): Show |
32 | HG00323.hp2 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.598-3380_598-3379i others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517797 | |||||||
| chr13:21517797 | A | G | 25 | a0001c0001t0002g0236 a0001c0001t0002g0250 a0001c0001t0002g0270 others(22): Show |
25 | HG00639.hp2 HG00738.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.598-3379T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517797 | |||||||
| chr13:21517797 | ACACGCG | A | 7 | a0001c0001t0001g0103 a0001c0001t0001g0109 a0001c0001t0001g0151 others(4): Show |
7 | HG00408.hp1 HG01243.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.598-3385_598-3380d others(8): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517797 | |||||||
| chr13:21517799 | A | ACACACAC others(5): Show |
2 | a0001c0002t0006g0028 a0001c0002t0006g0181 |
2 | HG00735.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.598-3382_598-3381i others(14): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517799 | |||||||
| chr13:21517799 | A | ACACACAC others(7): Show |
1 | a0001c0002t0006g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.598-3382_598-3381i others(16): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517799 | |||||||
| chr13:21517799 | A | ACG | 4 | a0001c0001t0002g0242 a0001c0001t0002g0269 a0001c0001t0002g0300 others(1): Show |
4 | HG00673.hp2 HG01123.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.598-3383_598-3382d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517799 | |||||||
| chr13:21517799 | A | G | 124 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(121): Show |
124 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.598-3381T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517799 | |||||||
| chr13:21517799 | ACG | A | 16 | a0001c0001t0001g0049 a0001c0001t0001g0056 a0001c0001t0001g0082 others(13): Show |
16 | HG02258.hp1 HG02572.hp2 HG02818.hp2 others(13): Show |
intron_variant | MODIFIER | c.598-3383_598-3382d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517799 | |||||||
| chr13:21517799 | ACGCG | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(72): Show |
77 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.598-3385_598-3382d others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517799 | |||||||
| chr13:21517801 | G | A | 14 | a0001c0001t0001g0081 a0001c0001t0001g0120 a0001c0001t0001g0166 others(11): Show |
14 | HG01192.hp2 HG01891.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.598-3383C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517801 | |||||||
| chr13:21517803 | G | A | 20 | a0001c0001t0001g0049 a0001c0001t0001g0081 a0001c0001t0001g0082 others(17): Show |
20 | HG01192.hp2 HG01891.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.598-3385C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517803 | |||||||
| chr13:21517804 | C | CGCGCGCG others(14): Show |
1 | a0001c0003t0003g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.598-3387_598-3386i others(23): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517804 | |||||||
| chr13:21517805 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0089 |
2 | NA18964.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.598-3387C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517805 | |||||||
| chr13:21517806 | C | CGCGCGCG others(4): Show |
1 | a0001c0001t0003g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.598-3389_598-3388i others(13): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517806 | |||||||
| chr13:21517813 | G | A | 1 | a0001c0001t0004g0182 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.598-3395C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517813 | |||||||
| chr13:21517815 | A | G | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.598-3397T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21517815 | |||||||
| chr13:21518121 | A | G | 105 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(102): Show |
105 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.597+3124T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21518121 | |||||||
| chr13:21518345 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.597+2900G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21518345 | |||||||
| chr13:21518435 | G | A | 6 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0036 others(3): Show |
6 | HG02258.hp1 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.597+2810C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21518435 | |||||||
| chr13:21518524 | A | G | 1 | a0001c0002t0005g0218 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.597+2721T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21518524 | |||||||
| chr13:21518616 | T | C | 1 | a0001c0002t0006g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.597+2629A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21518616 | |||||||
| chr13:21518623 | T | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(96): Show |
101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.597+2622A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21518623 | |||||||
| chr13:21518822 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(96): Show |
101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.597+2423A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21518822 | |||||||
| chr13:21518872 | A | C | 1 | a0001c0001t0002g0269 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.597+2373T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21518872 | |||||||
| chr13:21518890 | T | C | 1 | a0001c0002t0001g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.597+2355A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21518890 | |||||||
| chr13:21518912 | T | C | 7 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.597+2333A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21518912 | |||||||
| chr13:21519060 | G | A | 18 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(15): Show |
18 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.597+2185C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21519060 | |||||||
| chr13:21519091 | T | A | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.597+2154A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21519091 | |||||||
| chr13:21519105 | C | T | 2 | a0001c0001t0002g0272 a0001c0001t0002g0293 |
2 | NA18946.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.597+2140G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21519105 | |||||||
| chr13:21519168 | T | C | 1 | a0001c0001t0004g0182 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.597+2077A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21519168 | |||||||
| chr13:21519196 | A | T | 11 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(8): Show |
11 | HG00639.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.597+2049T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21519196 | |||||||
| chr13:21519218 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.597+2027C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21519218 | |||||||
| chr13:21519364 | G | A | 1 | a0001c0003t0003g0025 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.597+1881C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21519364 | |||||||
| chr13:21519502 | T | A | 1 | a0001c0001t0002g0254 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.597+1743A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21519502 | |||||||
| chr13:21519556 | G | A | 9 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.597+1689C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21519556 | |||||||
| chr13:21519685 | T | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(91): Show |
96 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.597+1560A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21519685 | |||||||
| chr13:21519696 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.597+1549G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21519696 | |||||||
| chr13:21519789 | T | C | 1 | a0001c0001t0002g0246 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.597+1456A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21519789 | |||||||
| chr13:21519827 | G | A | 1 | a0001c0001t0004g0180 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.597+1418C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21519827 | |||||||
| chr13:21519835 | T | C | 1 | a0001c0001t0002g0251 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.597+1410A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21519835 | |||||||
| chr13:21519969 | A | C | 1 | a0003c0007t0001g0219 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.597+1276T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21519969 | |||||||
| chr13:21520390 | C | T | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.597+855G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21520390 | |||||||
| chr13:21520478 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.597+767G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21520478 | |||||||
| chr13:21520660 | G | GT | 123 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(120): Show |
123 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.597+584dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21520660 | |||||||
| chr13:21520759 | C | T | 5 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
5 | HG01175.hp2 HG02735.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+486G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21520759 | |||||||
| chr13:21520872 | T | G | 1 | a0001c0001t0001g0202 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.597+373A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21520872 | |||||||
| chr13:21521230 | T | G | 1 | a0001c0001t0002g0274 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.597+15A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 6/11 | chr13 | 21521230 | |||||||
| chr13:21521428 | T | C | 8 | a0001c0001t0001g0175 a0001c0001t0003g0135 a0001c0001t0003g0136 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.515-101A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 5/11 | chr13 | 21521428 | |||||||
| chr13:21521523 | C | A | 3 | a0001c0001t0003g0041 a0001c0001t0003g0043 a0001c0001t0003g0046 |
3 | HG02109.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.515-196G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 5/11 | chr13 | 21521523 | |||||||
| chr13:21521836 | C | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(295): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.515-509G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 5/11 | chr13 | 21521836 | |||||||
| chr13:21522212 | T | G | 1 | a0001c0001t0001g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.514+391A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 5/11 | chr13 | 21522212 | |||||||
| chr13:21522472 | T | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(96): Show |
101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.514+131A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 5/11 | chr13 | 21522472 | |||||||
| chr13:21522526 | T | G | 4 | a0001c0002t0006g0028 a0001c0002t0006g0128 a0001c0002t0006g0181 others(1): Show |
4 | HG00735.hp2 HG02622.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.514+77A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 5/11 | chr13 | 21522526 | |||||||
| chr13:21522668 | A | G | 1 | a0001c0001t0002g0286 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.467-18T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21522668 | |||||||
| chr13:21522704 | T | C | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(295): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.467-54A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21522704 | |||||||
| chr13:21522916 | T | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0064 a0001c0001t0001g0074 others(1): Show |
4 | HG02735.hp1 HG03017.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-266A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21522916 | |||||||
| chr13:21523002 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.467-352C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21523002 | |||||||
| chr13:21523238 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.467-588A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21523238 | |||||||
| chr13:21523269 | T | C | 10 | a0001c0001t0002g0237 a0001c0001t0002g0262 a0001c0001t0002g0275 others(7): Show |
10 | HG01255.hp2 HG01433.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.467-619A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21523269 | |||||||
| chr13:21523314 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(92): Show |
97 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.467-664T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21523314 | |||||||
| chr13:21523361 | A | C | 9 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.467-711T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21523361 | |||||||
| chr13:21523415 | AACATCTC others(5): Show |
A | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.467-777_467-766del others(12): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21523415 | |||||||
| chr13:21523491 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(91): Show |
96 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.467-841G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21523491 | |||||||
| chr13:21523502 | G | A | 40 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(37): Show |
40 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.467-852C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21523502 | |||||||
| chr13:21523550 | T | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0176 |
2 | HG03490.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.467-900A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21523550 | |||||||
| chr13:21524074 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(91): Show |
96 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.467-1424G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21524074 | |||||||
| chr13:21524081 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.467-1431C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21524081 | |||||||
| chr13:21524134 | G | A | 1 | a0001c0001t0004g0185 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.467-1484C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21524134 | |||||||
| chr13:21524250 | T | C | 19 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(16): Show |
19 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.467-1600A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21524250 | |||||||
| chr13:21524800 | C | A | 1 | a0001c0001t0001g0165 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.467-2150G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21524800 | |||||||
| chr13:21524849 | G | A | 1 | a0001c0001t0002g0299 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.467-2199C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21524849 | |||||||
| chr13:21524973 | T | C | 11 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.467-2323A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21524973 | |||||||
| chr13:21524988 | C | G | 4 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(1): Show |
4 | HG01106.hp2 HG03704.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-2338G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21524988 | |||||||
| chr13:21525181 | A | AT | 80 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0059 others(77): Show |
80 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.467-2532dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525181 | |||||||
| chr13:21525181 | A | ATT | 33 | a0001c0001t0001g0002 a0001c0001t0001g0049 a0001c0001t0001g0074 others(30): Show |
34 | HG00673.hp1 HG00673.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.467-2533_467-2532d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525181 | |||||||
| chr13:21525181 | A | ATTT | 11 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0103 others(8): Show |
11 | HG00323.hp1 HG01175.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.467-2534_467-2532d others(5): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525181 | |||||||
| chr13:21525181 | AT | A | 23 | a0001c0001t0001g0052 a0001c0001t0001g0090 a0001c0001t0001g0099 others(20): Show |
23 | HG00323.hp2 HG01070.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.467-2532delA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525181 | |||||||
| chr13:21525181 | ATTTT | A | 30 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(27): Show |
30 | HG01175.hp2 HG01243.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.467-2535_467-2532d others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525181 | |||||||
| chr13:21525181 | ATTTTTTT others(4): Show |
A | 4 | a0001c0002t0006g0028 a0001c0002t0006g0128 a0001c0002t0006g0181 others(1): Show |
4 | HG00735.hp2 HG02622.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-2542_467-2532d others(13): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525181 | |||||||
| chr13:21525181 | ATTTTTTT others(5): Show |
A | 10 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.467-2543_467-2532d others(14): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525181 | |||||||
| chr13:21525229 | G | C | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.467-2579C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525229 | |||||||
| chr13:21525231 | C | T | 34 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(31): Show |
34 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.467-2581G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525231 | |||||||
| chr13:21525286 | A | G | 1 | a0001c0001t0003g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.467-2636T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525286 | |||||||
| chr13:21525316 | C | T | 2 | a0001c0001t0003g0174 a0001c0001t0003g0177 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.467-2666G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525316 | |||||||
| chr13:21525349 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.467-2699G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525349 | |||||||
| chr13:21525780 | T | C | 3 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0142 |
3 | HG02717.hp1 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.467-3130A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525780 | |||||||
| chr13:21525820 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.467-3170G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525820 | |||||||
| chr13:21525878 | C | T | 1 | a0001c0002t0005g0218 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.467-3228G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525878 | |||||||
| chr13:21525913 | C | CTTAT | 16 | a0001c0001t0002g0301 a0001c0001t0003g0135 a0001c0001t0003g0136 others(13): Show |
16 | HG00735.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.467-3267_467-3264d others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525913 | |||||||
| chr13:21525913 | C | CTTATTTA others(1): Show |
8 | a0001c0001t0003g0192 a0001c0002t0005g0210 a0001c0002t0005g0211 others(5): Show |
8 | HG02559.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.467-3271_467-3264d others(10): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525913 | |||||||
| chr13:21525913 | C | CTTATTTA others(5): Show |
2 | a0001c0002t0005g0209 a0001c0002t0005g0217 |
2 | HG01192.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.467-3275_467-3264d others(14): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525913 | |||||||
| chr13:21525913 | CTTAT | C | 114 | a0001c0001t0001g0067 a0001c0001t0001g0158 a0001c0001t0002g0221 others(111): Show |
114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.467-3267_467-3264d others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525913 | |||||||
| chr13:21525913 | CTTATTTA others(1): Show |
C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(133): Show |
138 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.467-3271_467-3264d others(10): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525913 | |||||||
| chr13:21525978 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.467-3328C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21525978 | |||||||
| chr13:21526004 | G | A | 1 | a0001c0003t0003g0010 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.467-3354C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21526004 | |||||||
| chr13:21526086 | T | A | 1 | a0001c0001t0004g0185 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.467-3436A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21526086 | |||||||
| chr13:21526113 | C | CT | 50 | a0001c0001t0001g0061 a0001c0001t0001g0089 a0001c0001t0001g0091 others(47): Show |
50 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.467-3464dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21526113 | |||||||
| chr13:21526113 | C | T | 1 | a0001c0001t0002g0279 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.467-3463G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21526113 | |||||||
| chr13:21526285 | C | G | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(293): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.467-3635G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21526285 | |||||||
| chr13:21526313 | A | G | 2 | a0001c0001t0003g0041 a0001c0001t0003g0043 |
2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.467-3663T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21526313 | |||||||
| chr13:21526751 | T | C | 94 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(91): Show |
94 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.467-4101A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21526751 | |||||||
| chr13:21526810 | GA | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(165): Show |
170 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.467-4161delT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21526810 | |||||||
| chr13:21526837 | G | A | 3 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 |
3 | HG02071.hp1 NA18974.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.467-4187C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21526837 | |||||||
| chr13:21526938 | A | G | 1 | a0001c0001t0002g0297 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.467-4288T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21526938 | |||||||
| chr13:21526951 | C | G | 1 | a0001c0001t0002g0264 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.467-4301G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21526951 | |||||||
| chr13:21527552 | A | G | 88 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.467-4902T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21527552 | |||||||
| chr13:21527800 | C | T | 1 | a0001c0001t0003g0039 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.467-5150G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21527800 | |||||||
| chr13:21527847 | C | T | 1 | a0001c0001t0004g0185 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.467-5197G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21527847 | |||||||
| chr13:21528156 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0114 |
2 | HG02602.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.467-5506C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21528156 | |||||||
| chr13:21528209 | G | A | 5 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
5 | HG01175.hp2 HG02735.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-5559C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21528209 | |||||||
| chr13:21528237 | T | C | 1 | a0001c0001t0002g0247 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.467-5587A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21528237 | |||||||
| chr13:21528339 | A | G | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.467-5689T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21528339 | |||||||
| chr13:21528516 | C | G | 88 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.467-5866G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21528516 | |||||||
| chr13:21528520 | A | G | 22 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(19): Show |
22 | HG00735.hp2 HG01243.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.467-5870T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21528520 | |||||||
| chr13:21528794 | T | A | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.467-6144A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21528794 | |||||||
| chr13:21528837 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(91): Show |
96 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.467-6187T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21528837 | |||||||
| chr13:21528874 | A | G | 1 | a0001c0002t0001g0034 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.467-6224T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21528874 | |||||||
| chr13:21528912 | T | C | 1 | a0001c0001t0002g0246 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.467-6262A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21528912 | |||||||
| chr13:21528970 | C | T | 3 | a0001c0002t0006g0028 a0001c0002t0006g0181 a0001c0002t0006g0190 |
3 | HG00735.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.467-6320G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21528970 | |||||||
| chr13:21529047 | G | A | 7 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(4): Show |
7 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.467-6397C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21529047 | |||||||
| chr13:21529155 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(91): Show |
96 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.467-6505T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21529155 | |||||||
| chr13:21529568 | T | G | 2 | a0001c0001t0002g0225 a0001c0001t0002g0228 |
2 | HG00733.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.467-6918A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21529568 | |||||||
| chr13:21529666 | C | T | 3 | a0001c0001t0002g0221 a0001c0001t0002g0246 a0001c0001t0002g0289 |
3 | NA18955.hp2 NA18956.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.467-7016G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21529666 | |||||||
| chr13:21529704 | G | C | 4 | a0001c0002t0006g0028 a0001c0002t0006g0128 a0001c0002t0006g0181 others(1): Show |
4 | HG00735.hp2 HG02622.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-7054C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21529704 | |||||||
| chr13:21529801 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.467-7151C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21529801 | |||||||
| chr13:21529886 | T | C | 6 | a0001c0001t0002g0274 a0001c0001t0002g0301 a0001c0001t0002g0302 others(3): Show |
6 | HG01069.hp1 HG01081.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-7236A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21529886 | |||||||
| chr13:21530207 | T | C | 44 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(41): Show |
44 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.467-7557A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21530207 | |||||||
| chr13:21530239 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(178): Show |
183 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.467-7589G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21530239 | |||||||
| chr13:21530250 | G | A | 1 | a0001c0002t0001g0034 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.467-7600C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21530250 | |||||||
| chr13:21530397 | C | T | 3 | a0001c0001t0003g0174 a0001c0001t0003g0177 a0001c0001t0004g0141 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.467-7747G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21530397 | |||||||
| chr13:21530468 | C | CA | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(299): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.467-7819dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21530468 | |||||||
| chr13:21530627 | T | C | 5 | a0001c0001t0001g0150 a0001c0003t0003g0015 a0001c0003t0003g0016 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-7977A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21530627 | |||||||
| chr13:21530702 | G | T | 27 | a0001c0001t0001g0119 a0001c0001t0001g0156 a0001c0001t0001g0157 others(24): Show |
27 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.467-8052C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21530702 | |||||||
| chr13:21530724 | G | A | 35 | a0001c0001t0002g0225 a0001c0001t0002g0226 a0001c0001t0002g0227 others(32): Show |
35 | HG00280.hp2 HG00423.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.467-8074C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21530724 | |||||||
| chr13:21530731 | C | T | 1 | a0001c0002t0006g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.467-8081G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21530731 | |||||||
| chr13:21530750 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.467-8100G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21530750 | |||||||
| chr13:21530775 | C | T | 1 | a0001c0002t0006g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.467-8125G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21530775 | |||||||
| chr13:21530789 | C | G | 28 | a0001c0001t0001g0048 a0001c0001t0001g0166 a0001c0001t0001g0201 others(25): Show |
28 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.467-8139G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21530789 | |||||||
| chr13:21530806 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.467-8156G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21530806 | |||||||
| chr13:21530830 | C | T | 1 | a0004c0009t0001g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.467-8180G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21530830 | |||||||
| chr13:21530930 | G | T | 1 | a0001c0002t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.467-8280C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21530930 | |||||||
| chr13:21531234 | A | G | 1 | a0001c0001t0002g0251 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.466+8068T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21531234 | |||||||
| chr13:21531354 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.466+7948G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21531354 | |||||||
| chr13:21531367 | T | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(82): Show |
87 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.466+7935A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21531367 | |||||||
| chr13:21531394 | G | A | 21 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0148 others(18): Show |
21 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.466+7908C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21531394 | |||||||
| chr13:21531489 | CAGACTAG others(5): Show |
C | 1 | a0001c0002t0006g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.466+7801_466+7812d others(14): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21531489 | |||||||
| chr13:21531527 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.466+7775C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21531527 | |||||||
| chr13:21531548 | G | A | 3 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0142 |
3 | HG02717.hp1 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.466+7754C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21531548 | |||||||
| chr13:21531617 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.466+7685G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21531617 | |||||||
| chr13:21531691 | G | C | 1 | a0001c0003t0003g0017 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.466+7611C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21531691 | |||||||
| chr13:21531819 | T | C | 13 | a0001c0001t0003g0174 a0001c0001t0003g0177 a0001c0001t0004g0141 others(10): Show |
13 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.466+7483A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21531819 | |||||||
| chr13:21531995 | A | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.466+7307T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21531995 | |||||||
| chr13:21532015 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.466+7287A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21532015 | |||||||
| chr13:21532104 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.466+7198A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21532104 | |||||||
| chr13:21532299 | C | T | 1 | a0001c0001t0002g0290 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.466+7003G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21532299 | |||||||
| chr13:21532333 | A | C | 1 | a0001c0001t0001g0159 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.466+6969T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21532333 | |||||||
| chr13:21532421 | T | C | 88 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.466+6881A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21532421 | |||||||
| chr13:21532706 | A | C | 1 | a0001c0001t0002g0240 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.466+6596T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21532706 | |||||||
| chr13:21532756 | T | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(286): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.466+6546A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21532756 | |||||||
| chr13:21532829 | G | A | 3 | a0001c0001t0002g0247 a0001c0001t0002g0270 a0001c0001t0002g0288 |
3 | HG02080.hp1 HG02165.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.466+6473C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21532829 | |||||||
| chr13:21532960 | G | C | 1 | a0001c0001t0002g0284 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.466+6342C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21532960 | |||||||
| chr13:21533075 | T | C | 2 | a0001c0001t0002g0225 a0001c0001t0002g0228 |
2 | HG00733.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.466+6227A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21533075 | |||||||
| chr13:21533098 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.466+6204G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21533098 | |||||||
| chr13:21533109 | G | C | 4 | a0001c0002t0006g0028 a0001c0002t0006g0128 a0001c0002t0006g0181 others(1): Show |
4 | HG00735.hp2 HG02622.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+6193C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21533109 | |||||||
| chr13:21533162 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.466+6140A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21533162 | |||||||
| chr13:21533216 | A | G | 2 | a0001c0001t0002g0225 a0001c0001t0002g0228 |
2 | HG00733.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.466+6086T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21533216 | |||||||
| chr13:21533324 | A | AT | 122 | a0001c0001t0001g0100 a0001c0001t0001g0125 a0001c0001t0002g0221 others(119): Show |
122 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.466+5977dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21533324 | |||||||
| chr13:21533342 | G | T | 9 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.466+5960C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21533342 | |||||||
| chr13:21533395 | C | T | 1 | a0001c0001t0003g0044 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.466+5907G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21533395 | |||||||
| chr13:21533514 | G | A | 8 | a0001c0001t0001g0175 a0001c0001t0003g0135 a0001c0001t0003g0136 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.466+5788C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21533514 | |||||||
| chr13:21533588 | G | T | 18 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(15): Show |
18 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.466+5714C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21533588 | |||||||
| chr13:21533664 | T | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0064 others(4): Show |
8 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.466+5638A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21533664 | |||||||
| chr13:21533733 | G | A | 1 | a0001c0002t0006g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.466+5569C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21533733 | |||||||
| chr13:21533733 | G | GTA | 3 | a0001c0002t0006g0028 a0001c0002t0006g0181 a0001c0002t0006g0190 |
3 | HG00735.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.466+5567_466+5568d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21533733 | |||||||
| chr13:21533995 | C | T | 126 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(123): Show |
126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.466+5307G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21533995 | |||||||
| chr13:21534044 | C | T | 11 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(8): Show |
11 | HG00639.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.466+5258G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21534044 | |||||||
| chr13:21534077 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.466+5225G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21534077 | |||||||
| chr13:21534096 | G | C | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02055.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.466+5206C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21534096 | |||||||
| chr13:21534212 | C | CT | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.466+5089dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21534212 | |||||||
| chr13:21534212 | CT | C | 7 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.466+5089delA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21534212 | |||||||
| chr13:21534212 | CTT | C | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.466+5088_466+5089d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21534212 | |||||||
| chr13:21534232 | G | C | 33 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(30): Show |
33 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.466+5070C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21534232 | |||||||
| chr13:21534272 | C | T | 1 | a0001c0001t0002g0251 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.466+5030G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21534272 | |||||||
| chr13:21534281 | C | A | 1 | a0001c0001t0008g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.466+5021G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21534281 | |||||||
| chr13:21534507 | C | T | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.466+4795G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21534507 | |||||||
| chr13:21534611 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.466+4691C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21534611 | |||||||
| chr13:21535045 | C | T | 7 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.466+4257G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21535045 | |||||||
| chr13:21535188 | T | C | 1 | a0001c0002t0006g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466+4114A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21535188 | |||||||
| chr13:21535413 | G | A | 34 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(31): Show |
34 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.466+3889C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21535413 | |||||||
| chr13:21535529 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0062 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.466+3773C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21535529 | |||||||
| chr13:21535648 | CA | C | 9 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0015 others(6): Show |
9 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.466+3653delT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21535648 | |||||||
| chr13:21535933 | C | T | 4 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0169 others(1): Show |
4 | HG01891.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+3369G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21535933 | |||||||
| chr13:21535965 | A | T | 1 | a0001c0001t0002g0284 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.466+3337T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21535965 | |||||||
| chr13:21536010 | C | T | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.466+3292G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21536010 | |||||||
| chr13:21536321 | T | C | 1 | a0001c0001t0002g0279 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.466+2981A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21536321 | |||||||
| chr13:21536326 | A | AT | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(83): Show |
88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.466+2975dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21536326 | |||||||
| chr13:21536337 | A | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(100): Show |
105 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.466+2965T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21536337 | |||||||
| chr13:21536356 | C | T | 18 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(15): Show |
18 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.466+2946G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21536356 | |||||||
| chr13:21536430 | C | T | 5 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0017 others(2): Show |
5 | HG01070.hp1 HG01433.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+2872G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21536430 | |||||||
| chr13:21536826 | T | G | 1 | a0001c0001t0004g0200 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.466+2476A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21536826 | |||||||
| chr13:21537133 | T | A | 1 | a0001c0001t0003g0194 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.466+2169A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21537133 | |||||||
| chr13:21537382 | C | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(82): Show |
87 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.466+1920G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21537382 | |||||||
| chr13:21537469 | CT | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(273): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.466+1832delA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21537469 | |||||||
| chr13:21537474 | T | C | 92 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(89): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.466+1828A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21537474 | |||||||
| chr13:21537556 | G | A | 126 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(123): Show |
126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.466+1746C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21537556 | |||||||
| chr13:21537660 | A | G | 126 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(123): Show |
126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.466+1642T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21537660 | |||||||
| chr13:21537661 | G | A | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG01175.hp2 HG02735.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+1641C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21537661 | |||||||
| chr13:21537900 | G | C | 1 | a0001c0001t0003g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.466+1402C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21537900 | |||||||
| chr13:21537930 | G | T | 1 | a0001c0001t0003g0196 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.466+1372C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21537930 | |||||||
| chr13:21538354 | G | A | 1 | a0001c0003t0003g0011 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.466+948C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538354 | |||||||
| chr13:21538354 | G | T | 1 | a0001c0001t0003g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.466+948C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538354 | |||||||
| chr13:21538394 | A | G | 11 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.466+908T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538394 | |||||||
| chr13:21538400 | G | A | 28 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(25): Show |
28 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.466+902C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538400 | |||||||
| chr13:21538421 | A | C | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.466+881T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538421 | |||||||
| chr13:21538439 | GTGCACAC others(17): Show |
G | 1 | a0001c0002t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.466+839_466+862del others(24): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538439 | |||||||
| chr13:21538562 | C | CA | 7 | a0001c0001t0002g0297 a0001c0001t0002g0305 a0001c0001t0003g0043 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.466+739dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538562 | |||||||
| chr13:21538562 | C | CAA | 124 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0224 others(121): Show |
124 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.466+738_466+739dup others(2): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538562 | |||||||
| chr13:21538562 | C | CAAA | 41 | a0001c0001t0001g0077 a0001c0001t0001g0201 a0001c0001t0001g0202 others(38): Show |
41 | HG00423.hp1 HG00673.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.466+737_466+739dup others(3): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538562 | |||||||
| chr13:21538562 | C | CAAAA | 43 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0050 others(40): Show |
44 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.466+736_466+739dup others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538562 | |||||||
| chr13:21538562 | C | CAAAAA | 39 | a0001c0001t0001g0001 a0001c0001t0001g0047 a0001c0001t0001g0049 others(36): Show |
40 | HG00408.hp1 HG01169.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.466+735_466+739dup others(5): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538562 | |||||||
| chr13:21538571 | A | G | 2 | a0001c0001t0003g0193 a0001c0001t0003g0198 |
2 | HG00735.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.466+731T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538571 | |||||||
| chr13:21538580 | A | C | 1 | a0004c0009t0001g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.466+722T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538580 | |||||||
| chr13:21538581 | C | A | 1 | a0001c0001t0007g0308 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.466+721G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538581 | |||||||
| chr13:21538714 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.466+588A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538714 | |||||||
| chr13:21538720 | G | A | 1 | a0001c0002t0001g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.466+582C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538720 | |||||||
| chr13:21538788 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(100): Show |
105 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.466+514C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538788 | |||||||
| chr13:21538857 | A | G | 4 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0169 others(1): Show |
4 | HG01891.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+445T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538857 | |||||||
| chr13:21538948 | T | C | 1 | a0001c0002t0006g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.466+354A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538948 | |||||||
| chr13:21538999 | C | A | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.466+303G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21538999 | |||||||
| chr13:21539044 | T | TG | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.466+257dupC | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21539044 | |||||||
| chr13:21539124 | T | C | 5 | a0001c0001t0008g0144 a0001c0002t0006g0028 a0001c0002t0006g0128 others(2): Show |
5 | HG00735.hp2 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+178A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 4/11 | chr13 | 21539124 | |||||||
| chr13:21539496 | C | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(159): Show |
164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.391-119G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 3/11 | chr13 | 21539496 | |||||||
| chr13:21539502 | T | C | 1 | a0001c0001t0002g0240 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.391-125A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 3/11 | chr13 | 21539502 | |||||||
| chr13:21539530 | C | T | 24 | a0001c0001t0001g0156 a0001c0003t0003g0003 a0001c0003t0003g0004 others(21): Show |
24 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.390+127G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 3/11 | chr13 | 21539530 | |||||||
| chr13:21539540 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.390+117G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 3/11 | chr13 | 21539540 | |||||||
| chr13:21539541 | G | A | 1 | a0001c0001t0004g0141 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.390+116C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 3/11 | chr13 | 21539541 | |||||||
| chr13:21539556 | C | A | 1 | a0001c0001t0003g0196 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.390+101G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 3/11 | chr13 | 21539556 | |||||||
| chr13:21539584 | C | T | 1 | a0002c0004t0003g0006 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.390+73G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 3/11 | chr13 | 21539584 | |||||||
| chr13:21539629 | A | T | 1 | a0001c0001t0002g0302 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.390+28T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 3/11 | chr13 | 21539629 | |||||||
| chr13:21540113 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.359-425G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21540113 | |||||||
| chr13:21540182 | T | C | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(293): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.359-494A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21540182 | |||||||
| chr13:21540197 | T | C | 1 | a0004c0009t0001g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.359-509A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21540197 | |||||||
| chr13:21540239 | A | C | 1 | a0001c0001t0002g0299 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.359-551T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21540239 | |||||||
| chr13:21540304 | C | CT | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(138): Show |
143 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.359-617dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21540304 | |||||||
| chr13:21540418 | C | T | 1 | a0001c0001t0002g0282 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.359-730G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21540418 | |||||||
| chr13:21540798 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.359-1110C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21540798 | |||||||
| chr13:21540864 | C | T | 11 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-1176G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21540864 | |||||||
| chr13:21540896 | A | G | 1 | a0001c0002t0005g0218 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.359-1208T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21540896 | |||||||
| chr13:21540989 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.359-1301G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21540989 | |||||||
| chr13:21541048 | T | C | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.359-1360A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21541048 | |||||||
| chr13:21541093 | G | T | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(293): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.359-1405C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21541093 | |||||||
| chr13:21541251 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.359-1563A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21541251 | |||||||
| chr13:21541252 | TA | T | 9 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.359-1565delT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21541252 | |||||||
| chr13:21541307 | T | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | HG00738.hp2 HG01168.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.359-1619A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21541307 | |||||||
| chr13:21541309 | C | T | 1 | a0001c0001t0004g0141 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.359-1621G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21541309 | |||||||
| chr13:21541312 | T | C | 1 | a0001c0001t0002g0281 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.359-1624A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21541312 | |||||||
| chr13:21541328 | G | A | 7 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-1640C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21541328 | |||||||
| chr13:21541682 | T | C | 22 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(19): Show |
22 | HG00735.hp2 HG01243.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.359-1994A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21541682 | |||||||
| chr13:21541683 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(83): Show |
88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.359-1995T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21541683 | |||||||
| chr13:21541799 | A | G | 1 | a0001c0002t0006g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.359-2111T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21541799 | |||||||
| chr13:21542134 | AGAGGTTG others(4): Show |
A | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.359-2457_359-2447d others(13): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21542134 | |||||||
| chr13:21542188 | A | G | 11 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-2500T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21542188 | |||||||
| chr13:21542349 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.359-2661G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21542349 | |||||||
| chr13:21542375 | C | T | 2 | a0001c0001t0002g0244 a0001c0001t0002g0295 |
2 | HG02027.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.359-2687G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21542375 | |||||||
| chr13:21542394 | A | G | 6 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0036 others(3): Show |
6 | HG02258.hp1 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-2706T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21542394 | |||||||
| chr13:21542665 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.359-2977A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21542665 | |||||||
| chr13:21542673 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.359-2985C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21542673 | |||||||
| chr13:21542682 | C | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG02735.hp2 HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.359-2994G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21542682 | |||||||
| chr13:21542852 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.359-3164T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21542852 | |||||||
| chr13:21542901 | C | T | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-3213G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21542901 | |||||||
| chr13:21542932 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.359-3244T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21542932 | |||||||
| chr13:21542948 | C | T | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(286): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.359-3260G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21542948 | |||||||
| chr13:21543036 | A | G | 5 | a0001c0001t0003g0041 a0001c0001t0003g0043 a0001c0001t0003g0044 others(2): Show |
5 | HG02109.hp2 HG02970.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-3348T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21543036 | |||||||
| chr13:21543259 | A | T | 1 | a0001c0002t0005g0209 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.359-3571T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21543259 | |||||||
| chr13:21543337 | G | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.359-3649C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21543337 | |||||||
| chr13:21543651 | C | A | 1 | a0001c0002t0005g0218 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.359-3963G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21543651 | |||||||
| chr13:21543700 | G | A | 34 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(31): Show |
34 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.359-4012C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21543700 | |||||||
| chr13:21543806 | G | GA | 189 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(186): Show |
189 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.359-4119dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21543806 | |||||||
| chr13:21543809 | A | AT | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.359-4122_359-4121i others(3): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21543809 | |||||||
| chr13:21544163 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.359-4475T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21544163 | |||||||
| chr13:21544242 | T | C | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.359-4554A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21544242 | |||||||
| chr13:21544296 | A | T | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-4608T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21544296 | |||||||
| chr13:21544498 | A | T | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.359-4810T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21544498 | |||||||
| chr13:21544516 | G | GA | 26 | a0001c0001t0001g0171 a0001c0001t0002g0231 a0001c0001t0002g0232 others(23): Show |
26 | HG01106.hp1 HG02055.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.359-4829dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21544516 | |||||||
| chr13:21544516 | G | GAA | 124 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0149 others(121): Show |
124 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.359-4830_359-4829d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21544516 | |||||||
| chr13:21544516 | G | GAAA | 28 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0164 others(25): Show |
28 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.359-4831_359-4829d others(5): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21544516 | |||||||
| chr13:21544516 | G | GAAAA | 11 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(8): Show |
11 | HG00639.hp2 HG00735.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-4832_359-4829d others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21544516 | |||||||
| chr13:21544532 | A | AAAAAC | 6 | a0001c0001t0001g0051 a0001c0001t0001g0084 a0001c0001t0001g0106 others(3): Show |
6 | HG01358.hp2 HG03017.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-4845_359-4844i others(7): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21544532 | |||||||
| chr13:21544532 | A | AAAAC | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(89): Show |
94 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.359-4845_359-4844i others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21544532 | |||||||
| chr13:21544532 | A | AAAC | 9 | a0001c0001t0001g0099 a0001c0001t0004g0212 a0001c0002t0005g0209 others(6): Show |
9 | HG01099.hp2 HG01192.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.359-4847_359-4845d others(5): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21544532 | |||||||
| chr13:21544662 | T | C | 92 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(89): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.359-4974A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21544662 | |||||||
| chr13:21544947 | G | A | 3 | a0001c0001t0002g0255 a0001c0001t0002g0303 a0001c0002t0006g0127 |
3 | HG02976.hp2 NA19001.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.359-5259C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21544947 | |||||||
| chr13:21545276 | C | T | 11 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(8): Show |
11 | HG00639.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-5588G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21545276 | |||||||
| chr13:21545278 | G | A | 2 | a0001c0001t0002g0285 a0001c0001t0002g0291 |
2 | HG00423.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.359-5590C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21545278 | |||||||
| chr13:21545392 | T | G | 8 | a0001c0001t0001g0175 a0001c0001t0003g0135 a0001c0001t0003g0136 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.359-5704A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21545392 | |||||||
| chr13:21545400 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.359-5712C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21545400 | |||||||
| chr13:21545402 | C | T | 5 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0037 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-5714G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21545402 | |||||||
| chr13:21545428 | C | A | 1 | a0001c0001t0002g0237 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.359-5740G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21545428 | |||||||
| chr13:21545549 | C | T | 33 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(30): Show |
33 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.359-5861G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21545549 | |||||||
| chr13:21545697 | T | C | 1 | a0001c0002t0005g0218 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.359-6009A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21545697 | |||||||
| chr13:21545698 | A | G | 4 | a0001c0001t0003g0174 a0001c0001t0003g0177 a0001c0001t0004g0141 others(1): Show |
4 | HG01884.hp1 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-6010T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21545698 | |||||||
| chr13:21545840 | AACT | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(83): Show |
88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.359-6155_359-6153d others(5): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21545840 | |||||||
| chr13:21545985 | C | T | 33 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(30): Show |
33 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.359-6297G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21545985 | |||||||
| chr13:21546061 | T | G | 1 | a0001c0001t0001g0084 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.359-6373A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21546061 | |||||||
| chr13:21546295 | C | CT | 8 | a0001c0001t0001g0104 a0001c0001t0002g0241 a0001c0001t0002g0269 others(5): Show |
8 | HG01123.hp1 HG01978.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.359-6608dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21546295 | |||||||
| chr13:21546295 | C | CTT | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(95): Show |
100 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.359-6609_359-6608d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21546295 | |||||||
| chr13:21546295 | C | CTTT | 7 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
7 | HG00741.hp2 HG01081.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.359-6610_359-6608d others(5): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21546295 | |||||||
| chr13:21546295 | CT | C | 24 | a0001c0001t0002g0272 a0001c0001t0002g0293 a0001c0003t0003g0003 others(21): Show |
24 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.359-6608delA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21546295 | |||||||
| chr13:21546390 | A | G | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(286): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.359-6702T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21546390 | |||||||
| chr13:21546495 | G | C | 1 | a0001c0001t0002g0249 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.359-6807C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21546495 | |||||||
| chr13:21546527 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(83): Show |
88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.359-6839G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21546527 | |||||||
| chr13:21546551 | G | A | 1 | a0001c0001t0003g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.359-6863C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21546551 | |||||||
| chr13:21546734 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.359-7046C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21546734 | |||||||
| chr13:21546762 | G | C | 2 | a0001c0001t0002g0260 a0001c0001t0002g0261 |
2 | NA19012.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.359-7074C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21546762 | |||||||
| chr13:21546794 | A | C | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-7106T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21546794 | |||||||
| chr13:21546946 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(127): Show |
132 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.359-7258A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21546946 | |||||||
| chr13:21547493 | G | T | 1 | a0001c0001t0001g0102 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.359-7805C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21547493 | |||||||
| chr13:21547717 | G | A | 31 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(28): Show |
31 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.359-8029C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21547717 | |||||||
| chr13:21547768 | C | A | 1 | a0001c0001t0004g0182 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.359-8080G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21547768 | |||||||
| chr13:21547798 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.359-8110A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21547798 | |||||||
| chr13:21547812 | C | G | 11 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-8124G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21547812 | |||||||
| chr13:21548054 | A | G | 1 | a0001c0003t0003g0022 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.359-8366T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21548054 | |||||||
| chr13:21548133 | T | A | 1 | a0001c0001t0001g0091 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.359-8445A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21548133 | |||||||
| chr13:21548186 | A | G | 7 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-8498T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21548186 | |||||||
| chr13:21548242 | G | C | 1 | a0001c0001t0001g0091 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.359-8554C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21548242 | |||||||
| chr13:21548338 | A | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.359-8650T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21548338 | |||||||
| chr13:21548921 | G | GT | 112 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0001g0071 others(109): Show |
112 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.359-9234dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21548921 | |||||||
| chr13:21548921 | G | GTT | 33 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(30): Show |
33 | HG00423.hp1 HG00733.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.359-9235_359-9234d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21548921 | |||||||
| chr13:21548921 | GT | G | 16 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0002t0001g0029 others(13): Show |
16 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.359-9234delA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21548921 | |||||||
| chr13:21548950 | G | A | 32 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(29): Show |
32 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.359-9262C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21548950 | |||||||
| chr13:21548997 | G | A | 107 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(104): Show |
107 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.359-9309C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21548997 | |||||||
| chr13:21549017 | C | T | 1 | a0001c0001t0003g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.359-9329G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549017 | |||||||
| chr13:21549070 | C | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0003g0027 |
3 | HG02818.hp2 HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.359-9382G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549070 | |||||||
| chr13:21549074 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.359-9386G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549074 | |||||||
| chr13:21549104 | C | T | 1 | a0001c0001t0002g0286 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.359-9416G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549104 | |||||||
| chr13:21549119 | C | T | 6 | a0001c0001t0002g0260 a0001c0001t0002g0261 a0001c0001t0002g0272 others(3): Show |
6 | HG01074.hp1 HG03209.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-9431G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549119 | |||||||
| chr13:21549120 | G | A | 4 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-9432C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549120 | |||||||
| chr13:21549132 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(93): Show |
98 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.359-9444A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549132 | |||||||
| chr13:21549150 | T | C | 8 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
8 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.359-9462A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549150 | |||||||
| chr13:21549165 | G | A | 90 | a0001c0001t0001g0047 a0001c0001t0001g0086 a0001c0001t0001g0087 others(87): Show |
90 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.359-9477C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549165 | |||||||
| chr13:21549195 | C | G | 1 | a0001c0001t0002g0238 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.359-9507G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549195 | |||||||
| chr13:21549208 | C | T | 1 | a0001c0006t0005g0214 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.359-9520G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549208 | |||||||
| chr13:21549215 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.359-9527A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549215 | |||||||
| chr13:21549217 | G | C | 1 | a0001c0001t0001g0126 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.359-9529C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549217 | |||||||
| chr13:21549221 | G | T | 1 | a0001c0002t0006g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.359-9533C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549221 | |||||||
| chr13:21549272 | C | T | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.359-9584G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549272 | |||||||
| chr13:21549314 | T | C | 3 | a0001c0001t0002g0256 a0001c0001t0002g0257 a0001c0001t0002g0258 |
3 | HG00280.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.359-9626A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549314 | |||||||
| chr13:21549461 | A | G | 126 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(123): Show |
126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.359-9773T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549461 | |||||||
| chr13:21549464 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.359-9776G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549464 | |||||||
| chr13:21549537 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.359-9849T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549537 | |||||||
| chr13:21549538 | C | T | 1 | a0001c0003t0003g0010 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.359-9850G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549538 | |||||||
| chr13:21549622 | C | CA | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.359-9935dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549622 | |||||||
| chr13:21549669 | G | A | 103 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(100): Show |
103 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.359-9981C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549669 | |||||||
| chr13:21549680 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.359-9992A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549680 | |||||||
| chr13:21549780 | AAT | A | 7 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-10094_359-1009 others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549780 | |||||||
| chr13:21549889 | G | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(112): Show |
117 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.359-10201C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549889 | |||||||
| chr13:21549903 | A | C | 1 | a0001c0003t0003g0025 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.359-10215T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21549903 | |||||||
| chr13:21550063 | C | T | 1 | a0001c0001t0002g0236 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.359-10375G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21550063 | |||||||
| chr13:21550193 | C | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(230): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.359-10505G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21550193 | |||||||
| chr13:21550225 | C | T | 1 | a0001c0003t0003g0010 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.359-10537G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21550225 | |||||||
| chr13:21550361 | A | G | 1 | a0001c0001t0002g0287 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.359-10673T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21550361 | |||||||
| chr13:21550515 | A | C | 1 | a0001c0001t0002g0247 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.359-10827T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21550515 | |||||||
| chr13:21550600 | C | T | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-10912G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21550600 | |||||||
| chr13:21550782 | TACA | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(82): Show |
87 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.359-11097_359-1109 others(7): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21550782 | |||||||
| chr13:21550871 | G | A | 1 | a0001c0001t0002g0271 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.359-11183C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21550871 | |||||||
| chr13:21551039 | C | T | 1 | a0004c0009t0001g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.359-11351G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21551039 | |||||||
| chr13:21551384 | T | C | 1 | a0001c0001t0002g0226 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.359-11696A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21551384 | |||||||
| chr13:21551398 | C | A | 29 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(26): Show |
29 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.359-11710G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21551398 | |||||||
| chr13:21551412 | C | T | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(293): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.359-11724G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21551412 | |||||||
| chr13:21551442 | A | T | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(284): Show |
289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.359-11754T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21551442 | |||||||
| chr13:21551487 | G | A | 1 | a0001c0002t0006g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.359-11799C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21551487 | |||||||
| chr13:21551659 | T | C | 22 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(19): Show |
22 | HG00639.hp2 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.359-11971A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21551659 | |||||||
| chr13:21551753 | C | G | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.359-12065G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21551753 | |||||||
| chr13:21551804 | A | G | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.359-12116T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21551804 | |||||||
| chr13:21551826 | C | T | 1 | a0001c0001t0002g0243 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.359-12138G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21551826 | |||||||
| chr13:21551881 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.359-12193G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21551881 | |||||||
| chr13:21551995 | T | C | 7 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-12307A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21551995 | |||||||
| chr13:21552023 | G | A | 2 | a0001c0002t0005g0209 a0001c0002t0005g0215 |
2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.359-12335C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21552023 | |||||||
| chr13:21552090 | C | T | 1 | a0001c0002t0006g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.359-12402G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21552090 | |||||||
| chr13:21552161 | C | G | 126 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(123): Show |
126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.359-12473G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21552161 | |||||||
| chr13:21552274 | T | C | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-12586A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21552274 | |||||||
| chr13:21552861 | C | T | 2 | a0001c0001t0002g0245 a0001c0001t0002g0298 |
2 | HG01255.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.359-13173G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21552861 | |||||||
| chr13:21552870 | T | C | 1 | a0001c0003t0003g0009 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.359-13182A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21552870 | |||||||
| chr13:21552903 | C | G | 3 | a0001c0002t0001g0029 a0001c0002t0001g0034 a0001c0002t0001g0035 |
3 | HG02630.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.359-13215G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21552903 | |||||||
| chr13:21552936 | C | G | 1 | a0001c0002t0001g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.359-13248G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21552936 | |||||||
| chr13:21552995 | C | T | 29 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(26): Show |
29 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.359-13307G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21552995 | |||||||
| chr13:21553224 | T | G | 1 | a0001c0002t0005g0218 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.359-13536A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21553224 | |||||||
| chr13:21553317 | G | A | 1 | a0001c0001t0002g0271 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.358+13480C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21553317 | |||||||
| chr13:21553332 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.358+13465C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21553332 | |||||||
| chr13:21553334 | C | T | 92 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(89): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.358+13463G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21553334 | |||||||
| chr13:21553392 | C | T | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+13405G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21553392 | |||||||
| chr13:21553404 | C | T | 2 | a0001c0001t0002g0235 a0001c0001t0002g0307 |
2 | HG03834.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.358+13393G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21553404 | |||||||
| chr13:21553557 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(287): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.358+13240A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21553557 | |||||||
| chr13:21553655 | A | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+13142T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21553655 | |||||||
| chr13:21553820 | T | C | 3 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0038 |
3 | HG02572.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.358+12977A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21553820 | |||||||
| chr13:21553851 | T | C | 1 | a0001c0002t0001g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.358+12946A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21553851 | |||||||
| chr13:21554128 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.358+12669G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21554128 | |||||||
| chr13:21554149 | C | T | 1 | a0001c0002t0006g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.358+12648G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21554149 | |||||||
| chr13:21554178 | G | A | 1 | a0001c0001t0007g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.358+12619C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21554178 | |||||||
| chr13:21554264 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+12533A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21554264 | |||||||
| chr13:21554356 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(103): Show |
108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.358+12441A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21554356 | |||||||
| chr13:21554484 | C | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(103): Show |
108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.358+12313G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21554484 | |||||||
| chr13:21554534 | T | C | 1 | a0001c0001t0002g0227 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.358+12263A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21554534 | |||||||
| chr13:21554539 | A | G | 11 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.358+12258T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21554539 | |||||||
| chr13:21554582 | A | G | 8 | a0001c0001t0001g0175 a0001c0001t0003g0135 a0001c0001t0003g0136 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.358+12215T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21554582 | |||||||
| chr13:21554635 | G | C | 4 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(1): Show |
4 | HG01106.hp2 HG03704.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+12162C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21554635 | |||||||
| chr13:21554706 | A | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0090 others(12): Show |
16 | HG00408.hp1 HG02027.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.358+12091T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21554706 | |||||||
| chr13:21554772 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.358+12025G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21554772 | |||||||
| chr13:21554847 | G | A | 2 | a0001c0001t0004g0182 a0001c0001t0004g0183 |
2 | HG00639.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.358+11950C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21554847 | |||||||
| chr13:21554874 | A | G | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+11923T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21554874 | |||||||
| chr13:21555146 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0172 |
2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.358+11651C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21555146 | |||||||
| chr13:21555189 | A | G | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.358+11608T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21555189 | |||||||
| chr13:21555288 | C | A | 1 | a0001c0003t0003g0012 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.358+11509G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21555288 | |||||||
| chr13:21555377 | A | T | 1 | a0001c0001t0003g0199 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.358+11420T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21555377 | |||||||
| chr13:21555608 | T | C | 1 | a0001c0001t0002g0259 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.358+11189A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21555608 | |||||||
| chr13:21555742 | T | TC | 19 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(16): Show |
19 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.358+11054dupG | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21555742 | |||||||
| chr13:21555748 | C | G | 2 | a0001c0001t0003g0132 a0001c0001t0003g0133 |
2 | HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.358+11049G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21555748 | |||||||
| chr13:21555782 | A | G | 3 | a0001c0001t0002g0234 a0001c0001t0002g0265 a0001c0001t0002g0267 |
3 | NA18950.hp1 NA18977.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.358+11015T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21555782 | |||||||
| chr13:21555951 | G | A | 1 | a0001c0001t0002g0284 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.358+10846C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21555951 | |||||||
| chr13:21556057 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.358+10740T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21556057 | |||||||
| chr13:21556087 | C | G | 1 | a0001c0001t0002g0246 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.358+10710G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21556087 | |||||||
| chr13:21556099 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.358+10698C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21556099 | |||||||
| chr13:21556624 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.358+10173G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21556624 | |||||||
| chr13:21556728 | C | T | 1 | a0001c0002t0006g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.358+10069G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21556728 | |||||||
| chr13:21556842 | C | T | 1 | a0001c0001t0002g0311 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.358+9955G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21556842 | |||||||
| chr13:21557021 | C | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+9776G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21557021 | |||||||
| chr13:21557095 | G | A | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(294): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.358+9702C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21557095 | |||||||
| chr13:21557127 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.358+9670T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21557127 | |||||||
| chr13:21557140 | G | A | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.358+9657C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21557140 | |||||||
| chr13:21557237 | T | A | 10 | a0001c0001t0004g0212 a0001c0002t0005g0209 a0001c0002t0005g0210 others(7): Show |
10 | HG01099.hp2 HG01192.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.358+9560A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21557237 | |||||||
| chr13:21557304 | A | C | 88 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.358+9493T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21557304 | |||||||
| chr13:21557452 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.358+9345C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21557452 | |||||||
| chr13:21557454 | A | C | 1 | a0001c0001t0002g0288 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.358+9343T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21557454 | |||||||
| chr13:21557533 | G | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0172 |
2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.358+9264C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21557533 | |||||||
| chr13:21557551 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+9246T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21557551 | |||||||
| chr13:21557614 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0172 |
2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.358+9183A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21557614 | |||||||
| chr13:21557662 | T | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+9135A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21557662 | |||||||
| chr13:21557758 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+9039G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21557758 | |||||||
| chr13:21557787 | C | T | 1 | a0001c0001t0007g0306 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.358+9010G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21557787 | |||||||
| chr13:21557813 | T | C | 5 | a0001c0001t0004g0178 a0001c0001t0004g0186 a0001c0001t0004g0187 others(2): Show |
5 | HG01891.hp1 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+8984A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21557813 | |||||||
| chr13:21558116 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0066 |
3 | HG01070.hp2 HG01071.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.358+8681C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21558116 | |||||||
| chr13:21558174 | T | C | 33 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(30): Show |
33 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.358+8623A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21558174 | |||||||
| chr13:21558184 | C | T | 1 | a0001c0008t0001g0057 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.358+8613G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21558184 | |||||||
| chr13:21558276 | C | T | 106 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(103): Show |
106 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.358+8521G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21558276 | |||||||
| chr13:21558381 | C | T | 2 | a0001c0001t0004g0182 a0001c0001t0004g0183 |
2 | HG00639.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.358+8416G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21558381 | |||||||
| chr13:21558382 | C | A | 4 | a0001c0001t0002g0260 a0001c0001t0002g0261 a0001c0001t0002g0272 others(1): Show |
4 | NA18946.hp2 NA18993.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+8415G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21558382 | |||||||
| chr13:21558444 | C | T | 1 | a0001c0001t0002g0282 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.358+8353G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21558444 | |||||||
| chr13:21558738 | A | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0090 others(12): Show |
16 | HG00408.hp1 HG02027.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.358+8059T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21558738 | |||||||
| chr13:21559037 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.358+7760C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21559037 | |||||||
| chr13:21559068 | T | G | 1 | a0001c0001t0002g0236 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.358+7729A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21559068 | |||||||
| chr13:21559339 | C | T | 19 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(16): Show |
19 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.358+7458G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21559339 | |||||||
| chr13:21559393 | C | T | 19 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(16): Show |
19 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.358+7404G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21559393 | |||||||
| chr13:21559451 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.358+7346A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21559451 | |||||||
| chr13:21559529 | C | CT | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(105): Show |
110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.358+7267dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21559529 | |||||||
| chr13:21559533 | T | C | 1 | a0001c0001t0002g0270 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.358+7264A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21559533 | |||||||
| chr13:21559590 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+7207A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21559590 | |||||||
| chr13:21559768 | A | C | 1 | a0001c0003t0003g0025 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.358+7029T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21559768 | |||||||
| chr13:21559898 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+6899G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21559898 | |||||||
| chr13:21559922 | G | T | 2 | a0001c0001t0004g0182 a0001c0001t0004g0183 |
2 | HG00639.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.358+6875C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21559922 | |||||||
| chr13:21560307 | ATATCCAA others(15): Show |
A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+6468_358+6489d others(24): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21560307 | |||||||
| chr13:21560470 | G | A | 2 | a0001c0001t0004g0182 a0001c0001t0004g0183 |
2 | HG00639.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.358+6327C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21560470 | |||||||
| chr13:21560560 | A | T | 1 | a0001c0001t0004g0184 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.358+6237T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21560560 | |||||||
| chr13:21560584 | T | C | 8 | a0001c0001t0002g0237 a0001c0001t0002g0262 a0001c0001t0002g0275 others(5): Show |
8 | HG01255.hp2 HG01433.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.358+6213A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21560584 | |||||||
| chr13:21560618 | CAA | C | 26 | a0001c0001t0002g0244 a0001c0001t0002g0283 a0001c0001t0002g0295 others(23): Show |
26 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.358+6177_358+6178d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21560618 | |||||||
| chr13:21560623 | A | C | 8 | a0001c0001t0001g0068 a0001c0001t0003g0135 a0001c0001t0003g0136 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.358+6174T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21560623 | |||||||
| chr13:21560623 | AAC | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0002g0221 others(98): Show |
102 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.358+6172_358+6173d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21560623 | |||||||
| chr13:21560701 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0066 |
3 | HG01070.hp2 HG01071.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.358+6096T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21560701 | |||||||
| chr13:21560752 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+6045A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21560752 | |||||||
| chr13:21560903 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+5894G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21560903 | |||||||
| chr13:21560949 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.358+5848G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21560949 | |||||||
| chr13:21561041 | C | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG00741.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.358+5756G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21561041 | |||||||
| chr13:21561080 | A | C | 5 | a0001c0001t0004g0182 a0001c0001t0004g0183 a0001c0002t0006g0028 others(2): Show |
5 | HG00639.hp2 HG00735.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+5717T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21561080 | |||||||
| chr13:21561093 | C | T | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(286): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.358+5704G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21561093 | |||||||
| chr13:21561373 | C | G | 2 | a0001c0001t0002g0245 a0001c0001t0002g0298 |
2 | HG01255.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.358+5424G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21561373 | |||||||
| chr13:21561390 | C | G | 5 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(2): Show |
5 | HG02055.hp2 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+5407G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21561390 | |||||||
| chr13:21561526 | T | A | 2 | a0001c0001t0002g0235 a0001c0001t0002g0307 |
2 | HG03834.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.358+5271A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21561526 | |||||||
| chr13:21561537 | TA | T | 10 | a0001c0001t0002g0238 a0001c0001t0003g0039 a0001c0001t0003g0129 others(7): Show |
10 | HG00140.hp1 HG01243.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.358+5259delT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21561537 | |||||||
| chr13:21561650 | G | T | 1 | a0001c0001t0003g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.358+5147C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21561650 | |||||||
| chr13:21561686 | GTTTC | G | 6 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
6 | NA18941.hp1 NA18974.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.358+5107_358+5110d others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21561686 | |||||||
| chr13:21561690 | CT | C | 99 | a0001c0001t0001g0052 a0001c0001t0001g0145 a0001c0001t0001g0146 others(96): Show |
99 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.358+5106delA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21561690 | |||||||
| chr13:21561690 | CTT | C | 104 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(101): Show |
104 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.358+5105_358+5106d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21561690 | |||||||
| chr13:21561730 | A | T | 1 | a0001c0001t0002g0238 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.358+5067T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21561730 | |||||||
| chr13:21561768 | G | GGTTA | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+5025_358+5028d others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21561768 | |||||||
| chr13:21561847 | G | C | 1 | a0001c0001t0003g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.358+4950C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21561847 | |||||||
| chr13:21561853 | C | T | 7 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+4944G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21561853 | |||||||
| chr13:21561915 | C | T | 1 | a0001c0001t0002g0236 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.358+4882G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21561915 | |||||||
| chr13:21562158 | G | C | 1 | a0001c0001t0003g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.358+4639C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21562158 | |||||||
| chr13:21562271 | T | C | 1 | a0001c0002t0001g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.358+4526A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21562271 | |||||||
| chr13:21562274 | G | A | 3 | a0001c0001t0002g0234 a0001c0001t0002g0265 a0001c0001t0002g0267 |
3 | NA18950.hp1 NA18977.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.358+4523C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21562274 | |||||||
| chr13:21562279 | G | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(286): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.358+4518C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21562279 | |||||||
| chr13:21562282 | G | A | 8 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(5): Show |
8 | HG01243.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.358+4515C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21562282 | |||||||
| chr13:21562301 | T | G | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+4496A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21562301 | |||||||
| chr13:21562441 | AT | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(105): Show |
110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.358+4355delA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21562441 | |||||||
| chr13:21562626 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+4171G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21562626 | |||||||
| chr13:21562627 | C | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+4170G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21562627 | |||||||
| chr13:21562632 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.358+4165G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21562632 | |||||||
| chr13:21562654 | T | C | 1 | a0001c0001t0002g0243 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.358+4143A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21562654 | |||||||
| chr13:21562681 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0172 |
2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.358+4116G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21562681 | |||||||
| chr13:21562991 | T | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+3806A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21562991 | |||||||
| chr13:21563127 | T | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(103): Show |
108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.358+3670A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563127 | |||||||
| chr13:21563230 | C | T | 10 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0001c0001t0001g0069 others(7): Show |
10 | HG01192.hp1 HG01928.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.358+3567G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563230 | |||||||
| chr13:21563245 | C | G | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+3552G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563245 | |||||||
| chr13:21563261 | C | T | 3 | a0001c0002t0001g0029 a0001c0002t0001g0034 a0001c0002t0001g0035 |
3 | HG02630.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.358+3536G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563261 | |||||||
| chr13:21563272 | G | A | 2 | a0001c0001t0004g0184 a0001c0001t0004g0185 |
2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.358+3525C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563272 | |||||||
| chr13:21563303 | A | C | 1 | a0001c0001t0008g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.358+3494T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563303 | |||||||
| chr13:21563361 | A | G | 12 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.358+3436T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563361 | |||||||
| chr13:21563372 | A | G | 1 | a0001c0002t0001g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.358+3425T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563372 | |||||||
| chr13:21563379 | C | A | 1 | a0001c0002t0001g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.358+3418G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563379 | |||||||
| chr13:21563386 | T | C | 1 | a0001c0002t0001g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.358+3411A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563386 | |||||||
| chr13:21563431 | G | A | 1 | a0001c0001t0003g0192 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.358+3366C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563431 | |||||||
| chr13:21563454 | C | CA | 102 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(99): Show |
102 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.358+3342dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563454 | |||||||
| chr13:21563454 | CA | C | 13 | a0001c0001t0001g0079 a0001c0001t0003g0194 a0001c0002t0001g0029 others(10): Show |
13 | HG01074.hp1 HG02015.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.358+3342delT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563454 | |||||||
| chr13:21563469 | A | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+3328T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563469 | |||||||
| chr13:21563550 | T | C | 3 | a0001c0002t0006g0028 a0001c0002t0006g0181 a0001c0002t0006g0190 |
3 | HG00735.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.358+3247A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563550 | |||||||
| chr13:21563604 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+3193G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563604 | |||||||
| chr13:21563628 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.358+3169G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563628 | |||||||
| chr13:21563708 | T | C | 1 | a0001c0003t0003g0013 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.358+3089A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563708 | |||||||
| chr13:21563813 | A | AT | 26 | a0001c0001t0002g0285 a0001c0001t0002g0291 a0001c0001t0008g0144 others(23): Show |
26 | HG00323.hp2 HG00423.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.358+2983dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563813 | |||||||
| chr13:21563813 | A | ATTT | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(101): Show |
106 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.358+2981_358+2983d others(5): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21563813 | |||||||
| chr13:21564070 | A | G | 14 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.358+2727T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21564070 | |||||||
| chr13:21564245 | T | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+2552A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21564245 | |||||||
| chr13:21564301 | G | A | 3 | a0001c0002t0006g0028 a0001c0002t0006g0181 a0001c0002t0006g0190 |
3 | HG00735.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.358+2496C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21564301 | |||||||
| chr13:21564309 | C | T | 5 | a0001c0001t0003g0174 a0001c0001t0003g0177 a0001c0001t0004g0141 others(2): Show |
5 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+2488G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21564309 | |||||||
| chr13:21564315 | G | T | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(294): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.358+2482C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21564315 | |||||||
| chr13:21564387 | G | A | 6 | a0001c0001t0003g0041 a0001c0001t0003g0042 a0001c0001t0003g0043 others(3): Show |
6 | HG02109.hp2 HG02970.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.358+2410C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21564387 | |||||||
| chr13:21564552 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(83): Show |
88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.358+2245A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21564552 | |||||||
| chr13:21564636 | A | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(294): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.358+2161T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21564636 | |||||||
| chr13:21564754 | T | C | 1 | a0001c0001t0004g0141 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.358+2043A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21564754 | |||||||
| chr13:21565132 | T | A | 4 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0169 others(1): Show |
4 | HG01891.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+1665A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21565132 | |||||||
| chr13:21565152 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+1645G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21565152 | |||||||
| chr13:21565227 | G | C | 6 | a0001c0001t0002g0237 a0001c0001t0002g0275 a0001c0001t0002g0276 others(3): Show |
6 | HG01255.hp2 HG01928.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.358+1570C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21565227 | |||||||
| chr13:21565295 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.358+1502T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21565295 | |||||||
| chr13:21565385 | C | T | 4 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+1412G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21565385 | |||||||
| chr13:21565426 | G | A | 1 | a0001c0001t0002g0302 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.358+1371C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21565426 | |||||||
| chr13:21565552 | A | G | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(293): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.358+1245T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21565552 | |||||||
| chr13:21565614 | C | T | 1 | a0001c0002t0006g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.358+1183G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21565614 | |||||||
| chr13:21565637 | G | A | 1 | a0001c0001t0002g0289 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.358+1160C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21565637 | |||||||
| chr13:21565639 | C | T | 33 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(30): Show |
33 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.358+1158G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21565639 | |||||||
| chr13:21565644 | C | G | 1 | a0001c0001t0007g0220 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.358+1153G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21565644 | |||||||
| chr13:21565847 | A | G | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+950T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21565847 | |||||||
| chr13:21565866 | C | T | 1 | a0003c0007t0001g0219 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.358+931G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21565866 | |||||||
| chr13:21566077 | C | T | 5 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(2): Show |
5 | HG02055.hp2 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+720G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21566077 | |||||||
| chr13:21566243 | A | G | 106 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(103): Show |
106 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.358+554T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21566243 | |||||||
| chr13:21566500 | A | AT | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.358+296dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21566500 | |||||||
| chr13:21566500 | AT | A | 21 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(18): Show |
21 | HG01099.hp2 HG01192.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.358+296delA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21566500 | |||||||
| chr13:21566684 | T | C | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+113A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21566684 | |||||||
| chr13:21566772 | TA | T | 36 | a0001c0001t0001g0126 a0001c0001t0001g0145 a0001c0001t0001g0146 others(33): Show |
36 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.358+24delT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 2/11 | chr13 | 21566772 | |||||||
| chr13:21567272 | A | T | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.211-328T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21567272 | |||||||
| chr13:21567387 | T | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(83): Show |
88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.211-443A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21567387 | |||||||
| chr13:21567448 | C | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(108): Show |
113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.211-504G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21567448 | |||||||
| chr13:21567615 | A | G | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(286): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.211-671T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21567615 | |||||||
| chr13:21568360 | G | GT | 34 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(31): Show |
34 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.211-1417dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21568360 | |||||||
| chr13:21568510 | A | G | 1 | a0001c0001t0002g0299 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.211-1566T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21568510 | |||||||
| chr13:21568844 | G | GT | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(182): Show |
187 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.211-1901dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21568844 | |||||||
| chr13:21568844 | G | GTT | 19 | a0001c0002t0006g0127 a0001c0003t0003g0003 a0001c0003t0003g0004 others(16): Show |
19 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.211-1902_211-1901d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21568844 | |||||||
| chr13:21568918 | A | G | 7 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.211-1974T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21568918 | |||||||
| chr13:21568961 | C | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.211-2017G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21568961 | |||||||
| chr13:21569179 | T | G | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0164 |
3 | HG02145.hp1 HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.211-2235A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21569179 | |||||||
| chr13:21569215 | G | C | 1 | a0001c0002t0006g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.211-2271C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21569215 | |||||||
| chr13:21569294 | C | T | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.211-2350G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21569294 | |||||||
| chr13:21569378 | A | G | 88 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.211-2434T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21569378 | |||||||
| chr13:21569564 | T | G | 33 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(30): Show |
33 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.211-2620A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21569564 | |||||||
| chr13:21569632 | A | C | 14 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.211-2688T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21569632 | |||||||
| chr13:21569743 | T | C | 8 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(5): Show |
8 | HG01243.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.211-2799A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21569743 | |||||||
| chr13:21569858 | A | C | 1 | a0001c0001t0002g0284 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.211-2914T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21569858 | |||||||
| chr13:21569907 | CCCACTGT others(5): Show |
C | 1 | a0001c0001t0003g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.211-2975_211-2964d others(14): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21569907 | |||||||
| chr13:21570187 | A | G | 8 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(5): Show |
8 | HG01243.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.211-3243T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21570187 | |||||||
| chr13:21570263 | A | G | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.211-3319T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21570263 | |||||||
| chr13:21570305 | T | TA | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.211-3362dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21570305 | |||||||
| chr13:21570341 | T | C | 1 | a0001c0001t0002g0263 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.211-3397A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21570341 | |||||||
| chr13:21570721 | AAAGGGAC others(416): Show |
A | 1 | a0001c0002t0001g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.211-4200_211-3778d others(2): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21570721 | |||||||
| chr13:21570757 | T | C | 1 | a0001c0001t0002g0298 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.211-3813A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21570757 | |||||||
| chr13:21570790 | C | T | 1 | a0001c0001t0004g0182 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.211-3846G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21570790 | |||||||
| chr13:21570921 | T | C | 92 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(89): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.211-3977A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21570921 | |||||||
| chr13:21570978 | C | CTTAATCT others(35): Show |
1 | a0001c0001t0001g0054 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.211-4076_211-4035d others(44): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21570978 | |||||||
| chr13:21571035 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.211-4091G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21571035 | |||||||
| chr13:21571150 | G | C | 2 | a0001c0001t0007g0308 a0001c0001t0007g0309 |
2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.211-4206C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21571150 | |||||||
| chr13:21571237 | A | G | 3 | a0001c0001t0002g0234 a0001c0001t0002g0265 a0001c0001t0002g0267 |
3 | NA18950.hp1 NA18977.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.211-4293T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21571237 | |||||||
| chr13:21571398 | T | A | 101 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(98): Show |
101 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.211-4454A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21571398 | |||||||
| chr13:21571399 | A | T | 1 | a0001c0001t0001g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.211-4455T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21571399 | |||||||
| chr13:21571410 | A | G | 2 | a0001c0001t0004g0182 a0001c0001t0004g0183 |
2 | HG00639.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.211-4466T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21571410 | |||||||
| chr13:21571411 | T | C | 9 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(6): Show |
9 | HG02109.hp1 HG02145.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.211-4467A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21571411 | |||||||
| chr13:21571469 | G | A | 129 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(126): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.211-4525C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21571469 | |||||||
| chr13:21571532 | C | T | 18 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(15): Show |
18 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.211-4588G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21571532 | |||||||
| chr13:21571601 | A | G | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(286): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.211-4657T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21571601 | |||||||
| chr13:21571688 | A | T | 1 | a0001c0003t0003g0013 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.211-4744T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21571688 | |||||||
| chr13:21571706 | A | G | 4 | a0001c0001t0003g0174 a0001c0001t0003g0177 a0001c0001t0004g0141 others(1): Show |
4 | HG01884.hp1 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-4762T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21571706 | |||||||
| chr13:21571802 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.211-4858G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21571802 | |||||||
| chr13:21571866 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(105): Show |
110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.211-4922A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21571866 | |||||||
| chr13:21572015 | C | A | 3 | a0001c0001t0003g0174 a0001c0001t0003g0177 a0001c0001t0004g0141 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.211-5071G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21572015 | |||||||
| chr13:21572058 | CTTAG | C | 6 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0036 others(3): Show |
6 | HG02258.hp1 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-5118_211-5115d others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21572058 | |||||||
| chr13:21572252 | C | T | 36 | a0001c0001t0001g0067 a0001c0001t0001g0108 a0001c0001t0001g0145 others(33): Show |
36 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.211-5308G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21572252 | |||||||
| chr13:21572263 | G | T | 1 | a0001c0001t0002g0271 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.211-5319C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21572263 | |||||||
| chr13:21572274 | A | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.211-5330T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21572274 | |||||||
| chr13:21572358 | T | C | 1 | a0001c0001t0003g0138 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.211-5414A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21572358 | |||||||
| chr13:21572420 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.211-5476A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21572420 | |||||||
| chr13:21572439 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.211-5495A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21572439 | |||||||
| chr13:21572547 | T | C | 4 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0264 others(1): Show |
4 | NA18941.hp2 NA18973.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-5603A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21572547 | |||||||
| chr13:21572558 | G | A | 1 | a0001c0001t0004g0141 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.211-5614C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21572558 | |||||||
| chr13:21572675 | C | T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0172 |
3 | HG01891.hp2 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.211-5731G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21572675 | |||||||
| chr13:21572700 | G | A | 1 | a0004c0009t0001g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.211-5756C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21572700 | |||||||
| chr13:21572942 | A | AC | 18 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(15): Show |
18 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.211-5999dupG | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21572942 | |||||||
| chr13:21572943 | C | CA | 160 | a0001c0001t0001g0090 a0001c0001t0001g0145 a0001c0001t0001g0146 others(157): Show |
160 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.211-6000dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21572943 | |||||||
| chr13:21572943 | C | CAA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(83): Show |
88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.211-6001_211-6000d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21572943 | |||||||
| chr13:21573117 | T | C | 1 | a0001c0001t0003g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.211-6173A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21573117 | |||||||
| chr13:21573156 | T | C | 3 | a0001c0002t0001g0029 a0001c0002t0001g0034 a0001c0002t0001g0035 |
3 | HG02630.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.211-6212A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21573156 | |||||||
| chr13:21573272 | ATTTTTTT others(5): Show |
A | 129 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(126): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.211-6340_211-6329d others(14): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21573272 | |||||||
| chr13:21573280 | G | GT | 21 | a0001c0001t0001g0049 a0001c0001t0001g0154 a0001c0001t0003g0039 others(18): Show |
21 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.211-6337dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21573280 | |||||||
| chr13:21573343 | G | A | 1 | a0001c0002t0006g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.211-6399C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21573343 | |||||||
| chr13:21573374 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.211-6430A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21573374 | |||||||
| chr13:21573434 | G | A | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02055.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.211-6490C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21573434 | |||||||
| chr13:21573514 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG01516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.211-6570G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21573514 | |||||||
| chr13:21573620 | A | G | 1 | a0001c0002t0006g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.211-6676T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21573620 | |||||||
| chr13:21573953 | C | T | 1 | a0001c0003t0003g0025 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.211-7009G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21573953 | |||||||
| chr13:21574011 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.211-7067G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21574011 | |||||||
| chr13:21574147 | A | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.211-7203T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21574147 | |||||||
| chr13:21574294 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(138): Show |
143 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.211-7350T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21574294 | |||||||
| chr13:21574363 | A | T | 2 | a0001c0001t0003g0193 a0001c0001t0003g0198 |
2 | HG00735.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.211-7419T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21574363 | |||||||
| chr13:21574382 | G | A | 1 | a0001c0001t0003g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.211-7438C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21574382 | |||||||
| chr13:21574559 | A | G | 129 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(126): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.211-7615T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21574559 | |||||||
| chr13:21574833 | T | C | 3 | a0001c0002t0001g0029 a0001c0002t0001g0034 a0001c0002t0001g0035 |
3 | HG02630.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.211-7889A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21574833 | |||||||
| chr13:21574838 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.211-7894T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21574838 | |||||||
| chr13:21575158 | TAC | T | 106 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(103): Show |
106 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.211-8216_211-8215d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21575158 | |||||||
| chr13:21575184 | T | C | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.211-8240A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21575184 | |||||||
| chr13:21575197 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(83): Show |
88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.211-8253T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21575197 | |||||||
| chr13:21575310 | C | T | 3 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0142 |
3 | HG02717.hp1 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.211-8366G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21575310 | |||||||
| chr13:21575421 | T | TA | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.211-8478dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21575421 | |||||||
| chr13:21575493 | T | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(286): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.211-8549A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21575493 | |||||||
| chr13:21575674 | G | A | 2 | a0001c0003t0003g0003 a0001c0003t0003g0004 |
2 | HG01433.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.211-8730C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21575674 | |||||||
| chr13:21575729 | C | CA | 41 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(38): Show |
41 | HG00738.hp2 HG01106.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.211-8786dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21575729 | |||||||
| chr13:21575729 | C | CAA | 11 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0150 others(8): Show |
11 | HG00639.hp1 HG01175.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.211-8787_211-8786d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21575729 | |||||||
| chr13:21575729 | CA | C | 114 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0055 others(111): Show |
114 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.211-8786delT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21575729 | |||||||
| chr13:21575729 | CAA | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(75): Show |
80 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.211-8787_211-8786d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21575729 | |||||||
| chr13:21576070 | A | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(83): Show |
88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.211-9126T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21576070 | |||||||
| chr13:21576096 | C | T | 1 | a0001c0002t0006g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.211-9152G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21576096 | |||||||
| chr13:21576099 | C | T | 11 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(8): Show |
11 | HG02109.hp1 HG02145.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.211-9155G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21576099 | |||||||
| chr13:21576189 | A | ACAGGATT others(35): Show |
1 | a0001c0001t0001g0163 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.211-9246_211-9245i others(44): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21576189 | |||||||
| chr13:21576190 | T | C | 1 | a0001c0001t0003g0198 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.211-9246A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21576190 | |||||||
| chr13:21576190 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.211-9246A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21576190 | |||||||
| chr13:21576313 | A | G | 2 | a0001c0001t0004g0182 a0001c0001t0004g0183 |
2 | HG00639.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.211-9369T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21576313 | |||||||
| chr13:21576346 | A | G | 4 | a0001c0003t0003g0015 a0001c0003t0003g0016 a0001c0003t0003g0019 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-9402T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21576346 | |||||||
| chr13:21576392 | C | G | 7 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.211-9448G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21576392 | |||||||
| chr13:21576600 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.211-9656A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21576600 | |||||||
| chr13:21576631 | C | T | 3 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0268 |
3 | NA18973.hp1 NA18984.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.211-9687G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21576631 | |||||||
| chr13:21576785 | C | T | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(293): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.211-9841G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21576785 | |||||||
| chr13:21577000 | GCAGATTT others(14): Show |
G | 1 | a0001c0001t0004g0141 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.211-10077_211-1005 others(25): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21577000 | |||||||
| chr13:21577066 | G | A | 1 | a0001c0001t0002g0267 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.211-10122C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21577066 | |||||||
| chr13:21577098 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.211-10154G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21577098 | |||||||
| chr13:21577229 | C | A | 7 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.211-10285G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21577229 | |||||||
| chr13:21577240 | T | A | 1 | a0001c0001t0004g0141 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.211-10296A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21577240 | |||||||
| chr13:21577295 | A | C | 113 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(110): Show |
113 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.211-10351T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21577295 | |||||||
| chr13:21577315 | C | T | 1 | a0001c0001t0004g0141 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.211-10371G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21577315 | |||||||
| chr13:21577655 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0066 |
3 | HG01070.hp2 HG01071.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.211-10711T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21577655 | |||||||
| chr13:21577708 | G | A | 3 | a0001c0002t0001g0029 a0001c0002t0001g0034 a0001c0002t0001g0035 |
3 | HG02630.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.211-10764C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21577708 | |||||||
| chr13:21577729 | C | T | 1 | a0001c0001t0003g0043 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.211-10785G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21577729 | |||||||
| chr13:21577737 | A | G | 129 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(126): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.211-10793T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21577737 | |||||||
| chr13:21577804 | C | CA | 60 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0088 others(57): Show |
60 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.211-10861dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21577804 | |||||||
| chr13:21577804 | C | CAA | 7 | a0001c0001t0001g0146 a0001c0001t0001g0150 a0001c0001t0001g0164 others(4): Show |
7 | HG01175.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.211-10862_211-1086 others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21577804 | |||||||
| chr13:21577804 | CA | C | 25 | a0001c0001t0001g0065 a0001c0001t0001g0092 a0001c0001t0001g0117 others(22): Show |
25 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.211-10861delT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21577804 | |||||||
| chr13:21577847 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.211-10903G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21577847 | |||||||
| chr13:21577970 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.211-11026G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21577970 | |||||||
| chr13:21577986 | AAAT | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(83): Show |
88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.211-11045_211-1104 others(7): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21577986 | |||||||
| chr13:21578900 | C | T | 92 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(89): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.211-11956G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21578900 | |||||||
| chr13:21579022 | T | C | 2 | a0001c0001t0003g0174 a0001c0001t0003g0177 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.211-12078A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21579022 | |||||||
| chr13:21579065 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.211-12121T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21579065 | |||||||
| chr13:21579141 | A | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(196): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.211-12197T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21579141 | |||||||
| chr13:21579220 | CTTG | C | 3 | a0001c0003t0003g0022 a0001c0003t0003g0023 a0001c0003t0003g0024 |
3 | HG01106.hp2 HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.211-12279_211-1227 others(7): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21579220 | |||||||
| chr13:21579343 | C | CT | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(240): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.211-12400dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21579343 | |||||||
| chr13:21579343 | C | CTT | 10 | a0001c0001t0001g0064 a0001c0001t0001g0100 a0001c0001t0001g0148 others(7): Show |
10 | HG01243.hp1 HG02738.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.211-12401_211-1240 others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21579343 | |||||||
| chr13:21579377 | G | A | 2 | a0001c0001t0002g0231 a0001c0001t0002g0232 |
2 | NA19000.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.211-12433C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21579377 | |||||||
| chr13:21579388 | T | C | 8 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(5): Show |
8 | HG01243.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.211-12444A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21579388 | |||||||
| chr13:21579419 | C | A | 6 | a0001c0001t0002g0237 a0001c0001t0002g0275 a0001c0001t0002g0276 others(3): Show |
6 | HG01255.hp2 HG01928.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.211-12475G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21579419 | |||||||
| chr13:21579528 | G | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(196): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.211-12584C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21579528 | |||||||
| chr13:21579558 | T | C | 1 | a0001c0001t0002g0280 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.211-12614A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21579558 | |||||||
| chr13:21579746 | T | C | 88 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.211-12802A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21579746 | |||||||
| chr13:21579792 | T | C | 1 | a0001c0001t0002g0302 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.211-12848A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21579792 | |||||||
| chr13:21579812 | C | A | 1 | a0001c0001t0003g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.211-12868G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21579812 | |||||||
| chr13:21580073 | T | C | 1 | a0001c0001t0002g0286 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.211-13129A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21580073 | |||||||
| chr13:21580583 | T | TACTCTTA others(14): Show |
84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(81): Show |
86 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.211-13660_211-1364 others(25): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21580583 | |||||||
| chr13:21580583 | T | TACTCTTA others(56): Show |
1 | a0001c0008t0001g0057 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.211-13640_211-1363 others(67): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21580583 | |||||||
| chr13:21580638 | G | A | 8 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(5): Show |
8 | HG01243.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.211-13694C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21580638 | |||||||
| chr13:21580713 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.211-13769A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21580713 | |||||||
| chr13:21580951 | A | G | 9 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.211-14007T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21580951 | |||||||
| chr13:21581013 | C | T | 18 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(15): Show |
18 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.211-14069G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21581013 | |||||||
| chr13:21581094 | A | G | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.211-14150T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21581094 | |||||||
| chr13:21581108 | A | C | 1 | a0001c0002t0005g0209 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.211-14164T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21581108 | |||||||
| chr13:21581202 | C | T | 19 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(16): Show |
19 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.211-14258G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21581202 | |||||||
| chr13:21581227 | C | T | 1 | a0001c0002t0006g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.211-14283G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21581227 | |||||||
| chr13:21581266 | C | T | 14 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.211-14322G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21581266 | |||||||
| chr13:21581275 | A | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(196): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.211-14331T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21581275 | |||||||
| chr13:21581536 | A | G | 3 | a0001c0002t0006g0028 a0001c0002t0006g0181 a0001c0002t0006g0190 |
3 | HG00735.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.211-14592T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21581536 | |||||||
| chr13:21581551 | C | A | 8 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(5): Show |
8 | HG01243.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.211-14607G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21581551 | |||||||
| chr13:21581642 | G | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(196): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.211-14698C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21581642 | |||||||
| chr13:21581764 | A | C | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(233): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.211-14820T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21581764 | |||||||
| chr13:21582021 | C | G | 7 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.211-15077G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21582021 | |||||||
| chr13:21582028 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.211-15084C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21582028 | |||||||
| chr13:21582055 | T | A | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(293): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.211-15111A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21582055 | |||||||
| chr13:21582251 | TA | T | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(286): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.211-15308delT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21582251 | |||||||
| chr13:21582281 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.211-15337G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21582281 | |||||||
| chr13:21582430 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.211-15486T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21582430 | |||||||
| chr13:21582568 | C | T | 1 | a0001c0002t0006g0028 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.211-15624G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21582568 | |||||||
| chr13:21582693 | C | T | 1 | a0001c0001t0003g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.211-15749G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21582693 | |||||||
| chr13:21582754 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(230): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.211-15810A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21582754 | |||||||
| chr13:21582774 | G | A | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.211-15830C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21582774 | |||||||
| chr13:21582874 | CA | C | 8 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(5): Show |
8 | HG01243.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.211-15931delT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21582874 | |||||||
| chr13:21582952 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.211-16008G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21582952 | |||||||
| chr13:21582974 | G | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(286): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.211-16030C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21582974 | |||||||
| chr13:21582986 | T | C | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0005c0005t0001g0026 |
3 | HG03041.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.211-16042A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21582986 | |||||||
| chr13:21583046 | G | C | 1 | a0001c0001t0002g0300 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.211-16102C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21583046 | |||||||
| chr13:21583126 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(195): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.211-16182T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21583126 | |||||||
| chr13:21583138 | C | T | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.211-16194G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21583138 | |||||||
| chr13:21583251 | T | C | 1 | a0001c0001t0003g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.211-16307A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21583251 | |||||||
| chr13:21583543 | T | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(286): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.211-16599A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21583543 | |||||||
| chr13:21583655 | A | G | 1 | a0001c0001t0007g0308 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.211-16711T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21583655 | |||||||
| chr13:21583846 | A | C | 8 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(5): Show |
8 | HG01243.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.211-16902T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21583846 | |||||||
| chr13:21583951 | C | T | 34 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(31): Show |
34 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.211-17007G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21583951 | |||||||
| chr13:21583964 | A | G | 1 | a0001c0001t0002g0238 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.211-17020T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21583964 | |||||||
| chr13:21584041 | T | G | 4 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(1): Show |
4 | HG01106.hp2 HG03704.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-17097A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21584041 | |||||||
| chr13:21584128 | G | A | 88 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.211-17184C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21584128 | |||||||
| chr13:21584163 | G | A | 3 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 |
3 | HG01167.hp1 HG01169.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.211-17219C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21584163 | |||||||
| chr13:21584388 | C | CA | 32 | a0001c0001t0001g0049 a0001c0001t0001g0123 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.211-17445dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21584388 | |||||||
| chr13:21584424 | A | G | 14 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.211-17480T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21584424 | |||||||
| chr13:21584511 | G | C | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.211-17567C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21584511 | |||||||
| chr13:21584592 | T | C | 1 | a0001c0001t0002g0296 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.211-17648A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21584592 | |||||||
| chr13:21584837 | T | C | 2 | a0001c0001t0003g0174 a0001c0001t0003g0177 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.211-17893A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21584837 | |||||||
| chr13:21584862 | C | T | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(294): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.211-17918G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21584862 | |||||||
| chr13:21584896 | T | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(196): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.211-17952A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21584896 | |||||||
| chr13:21585003 | G | A | 1 | a0001c0001t0004g0189 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.211-18059C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21585003 | |||||||
| chr13:21585138 | A | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(196): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.211-18194T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21585138 | |||||||
| chr13:21585657 | T | C | 8 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(5): Show |
8 | HG01243.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+18282A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21585657 | |||||||
| chr13:21585997 | C | G | 1 | a0001c0003t0003g0021 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.210+17942G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21585997 | |||||||
| chr13:21586197 | C | T | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(294): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.210+17742G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21586197 | |||||||
| chr13:21586355 | G | A | 37 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(34): Show |
37 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.210+17584C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21586355 | |||||||
| chr13:21586465 | C | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(196): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.210+17474G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21586465 | |||||||
| chr13:21586530 | G | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0090 others(13): Show |
17 | HG00408.hp1 HG02027.hp1 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.210+17409C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21586530 | |||||||
| chr13:21586570 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.210+17369C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21586570 | |||||||
| chr13:21586577 | T | C | 6 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0036 others(3): Show |
6 | HG02258.hp1 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+17362A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21586577 | |||||||
| chr13:21586709 | C | T | 4 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(1): Show |
4 | HG01106.hp2 HG03704.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+17230G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21586709 | |||||||
| chr13:21586722 | A | G | 30 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(27): Show |
30 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.210+17217T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21586722 | |||||||
| chr13:21586818 | C | G | 1 | a0001c0001t0003g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.210+17121G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21586818 | |||||||
| chr13:21587147 | C | T | 1 | a0001c0001t0003g0191 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.210+16792G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21587147 | |||||||
| chr13:21587458 | C | G | 88 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.210+16481G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21587458 | |||||||
| chr13:21587498 | A | T | 14 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.210+16441T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21587498 | |||||||
| chr13:21587524 | T | C | 4 | a0001c0001t0003g0174 a0001c0001t0003g0177 a0001c0001t0004g0141 others(1): Show |
4 | HG01884.hp1 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+16415A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21587524 | |||||||
| chr13:21587631 | G | A | 4 | a0001c0001t0002g0236 a0001c0001t0003g0027 a0001c0001t0004g0182 others(1): Show |
4 | HG00639.hp2 HG02257.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+16308C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21587631 | |||||||
| chr13:21587666 | T | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(286): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.210+16273A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21587666 | |||||||
| chr13:21587755 | C | T | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(293): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.210+16184G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21587755 | |||||||
| chr13:21588000 | A | G | 8 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(5): Show |
8 | HG01243.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+15939T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21588000 | |||||||
| chr13:21588065 | G | A | 9 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.210+15874C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21588065 | |||||||
| chr13:21588273 | C | T | 11 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(8): Show |
11 | HG02109.hp1 HG02145.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.210+15666G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21588273 | |||||||
| chr13:21588487 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.210+15452C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21588487 | |||||||
| chr13:21588517 | T | C | 92 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(89): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.210+15422A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21588517 | |||||||
| chr13:21588775 | C | A | 9 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.210+15164G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21588775 | |||||||
| chr13:21588879 | T | C | 4 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0169 others(1): Show |
4 | HG01891.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+15060A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21588879 | |||||||
| chr13:21588941 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.210+14998T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21588941 | |||||||
| chr13:21589072 | G | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(196): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.210+14867C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21589072 | |||||||
| chr13:21589156 | T | C | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(300): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.210+14783A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21589156 | |||||||
| chr13:21589292 | C | T | 7 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.210+14647G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21589292 | |||||||
| chr13:21589428 | T | C | 1 | a0001c0001t0002g0297 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.210+14511A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21589428 | |||||||
| chr13:21589492 | A | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG00741.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.210+14447T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21589492 | |||||||
| chr13:21589527 | T | C | 34 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(31): Show |
34 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.210+14412A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21589527 | |||||||
| chr13:21589557 | T | C | 2 | a0001c0002t0001g0029 a0001c0002t0001g0035 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.210+14382A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21589557 | |||||||
| chr13:21589584 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.210+14355G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21589584 | |||||||
| chr13:21589764 | T | C | 33 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(30): Show |
33 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.210+14175A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21589764 | |||||||
| chr13:21589786 | TAGTG | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.210+14149_210+1415 others(8): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21589786 | |||||||
| chr13:21589798 | T | C | 5 | a0001c0001t0002g0230 a0001c0001t0002g0281 a0001c0001t0002g0282 others(2): Show |
5 | HG01978.hp2 NA18943.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+14141A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21589798 | |||||||
| chr13:21589887 | GA | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.210+14051delT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21589887 | |||||||
| chr13:21589888 | A | G | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+14051T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21589888 | |||||||
| chr13:21590040 | TATA | T | 3 | a0001c0001t0003g0174 a0001c0001t0003g0177 a0001c0001t0004g0141 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.210+13896_210+1389 others(7): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21590040 | |||||||
| chr13:21590355 | C | G | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+13584G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21590355 | |||||||
| chr13:21590598 | C | T | 1 | a0001c0001t0004g0141 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.210+13341G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21590598 | |||||||
| chr13:21590602 | C | G | 14 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.210+13337G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21590602 | |||||||
| chr13:21590727 | T | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(294): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.210+13212A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21590727 | |||||||
| chr13:21590729 | T | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(196): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.210+13210A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21590729 | |||||||
| chr13:21590916 | G | A | 2 | a0001c0003t0003g0011 a0001c0003t0003g0012 |
2 | HG01358.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.210+13023C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21590916 | |||||||
| chr13:21590959 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.210+12980G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21590959 | |||||||
| chr13:21590961 | A | G | 1 | a0001c0001t0002g0290 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.210+12978T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21590961 | |||||||
| chr13:21591027 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.210+12912G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21591027 | |||||||
| chr13:21591089 | C | T | 1 | a0001c0002t0005g0216 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.210+12850G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21591089 | |||||||
| chr13:21591123 | T | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(196): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.210+12816A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21591123 | |||||||
| chr13:21591138 | G | A | 1 | a0001c0001t0002g0230 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.210+12801C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21591138 | |||||||
| chr13:21591202 | C | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(195): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.210+12737G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21591202 | |||||||
| chr13:21591267 | AAAAAAAG | A | 10 | a0001c0001t0004g0212 a0001c0002t0005g0209 a0001c0002t0005g0210 others(7): Show |
10 | HG01099.hp2 HG01192.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.210+12665_210+1267 others(11): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21591267 | |||||||
| chr13:21591296 | T | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0171 |
2 | HG01106.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.210+12643A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21591296 | |||||||
| chr13:21591448 | G | A | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.210+12491C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21591448 | |||||||
| chr13:21591458 | G | C | 1 | a0001c0003t0003g0013 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.210+12481C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21591458 | |||||||
| chr13:21591574 | ATTC | A | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.210+12362_210+1236 others(7): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21591574 | |||||||
| chr13:21591582 | T | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(196): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.210+12357A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21591582 | |||||||
| chr13:21591824 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.210+12115T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21591824 | |||||||
| chr13:21592051 | CA | C | 28 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0099 others(25): Show |
28 | HG01069.hp2 HG01071.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.210+11887delT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21592051 | |||||||
| chr13:21592051 | CAA | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(109): Show |
114 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.210+11886_210+1188 others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21592051 | |||||||
| chr13:21592179 | G | A | 1 | a0001c0001t0003g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.210+11760C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21592179 | |||||||
| chr13:21592189 | C | G | 1 | a0001c0001t0002g0237 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.210+11750G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21592189 | |||||||
| chr13:21592373 | C | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(196): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.210+11566G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21592373 | |||||||
| chr13:21592504 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.210+11435G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21592504 | |||||||
| chr13:21592517 | G | GAC | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(293): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.210+11421_210+1142 others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21592517 | |||||||
| chr13:21592555 | C | T | 1 | a0001c0001t0002g0236 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.210+11384G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21592555 | |||||||
| chr13:21592601 | G | A | 1 | a0004c0009t0001g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.210+11338C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21592601 | |||||||
| chr13:21592660 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.210+11279T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21592660 | |||||||
| chr13:21592680 | T | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(294): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.210+11259A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21592680 | |||||||
| chr13:21592714 | C | T | 3 | a0001c0001t0003g0174 a0001c0001t0003g0177 a0001c0001t0004g0141 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.210+11225G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21592714 | |||||||
| chr13:21592715 | G | A | 14 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.210+11224C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21592715 | |||||||
| chr13:21592986 | T | C | 8 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(5): Show |
8 | HG01243.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+10953A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21592986 | |||||||
| chr13:21593043 | A | C | 1 | a0001c0001t0001g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.210+10896T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21593043 | |||||||
| chr13:21593138 | C | A | 5 | a0001c0001t0002g0225 a0001c0001t0002g0226 a0001c0001t0002g0227 others(2): Show |
5 | HG00733.hp2 HG01175.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+10801G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21593138 | |||||||
| chr13:21593166 | G | A | 1 | a0001c0002t0006g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.210+10773C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21593166 | |||||||
| chr13:21593217 | G | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(286): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.210+10722C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21593217 | |||||||
| chr13:21593501 | TA | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(195): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.210+10437delT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21593501 | |||||||
| chr13:21593555 | CAA | C | 11 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(8): Show |
11 | HG02109.hp1 HG02145.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.210+10382_210+1038 others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21593555 | |||||||
| chr13:21593571 | C | CA | 214 | a0001c0001t0001g0001 a0001c0001t0001g0047 a0001c0001t0001g0048 others(211): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.210+10367dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21593571 | |||||||
| chr13:21593571 | C | CAA | 41 | a0001c0001t0001g0002 a0001c0001t0001g0049 a0001c0001t0001g0100 others(38): Show |
42 | HG00323.hp1 HG00639.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.210+10366_210+1036 others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21593571 | |||||||
| chr13:21593634 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0126 |
3 | NA18946.hp1 NA18956.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.210+10305G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21593634 | |||||||
| chr13:21593671 | T | C | 1 | a0001c0001t0007g0306 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.210+10268A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21593671 | |||||||
| chr13:21593740 | C | T | 2 | a0001c0003t0003g0003 a0001c0003t0003g0004 |
2 | HG01433.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.210+10199G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21593740 | |||||||
| chr13:21594090 | A | G | 1 | a0001c0002t0006g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.210+9849T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21594090 | |||||||
| chr13:21594260 | G | A | 1 | a0001c0001t0002g0288 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.210+9679C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21594260 | |||||||
| chr13:21594354 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.210+9585C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21594354 | |||||||
| chr13:21594409 | G | C | 3 | a0001c0002t0006g0028 a0001c0002t0006g0181 a0001c0002t0006g0190 |
3 | HG00735.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.210+9530C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21594409 | |||||||
| chr13:21594618 | G | A | 1 | a0001c0001t0002g0295 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.210+9321C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21594618 | |||||||
| chr13:21594655 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG00733.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.210+9284T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21594655 | |||||||
| chr13:21594752 | A | G | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.210+9187T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21594752 | |||||||
| chr13:21594867 | C | T | 127 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(124): Show |
127 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.210+9072G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21594867 | |||||||
| chr13:21594948 | T | C | 3 | a0001c0002t0006g0028 a0001c0002t0006g0181 a0001c0002t0006g0190 |
3 | HG00735.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.210+8991A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21594948 | |||||||
| chr13:21595182 | G | A | 1 | a0001c0003t0003g0021 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.210+8757C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21595182 | |||||||
| chr13:21595184 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.210+8755G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21595184 | |||||||
| chr13:21595650 | T | A | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(292): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.210+8289A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21595650 | |||||||
| chr13:21595685 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(105): Show |
110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.210+8254A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21595685 | |||||||
| chr13:21596121 | T | C | 1 | a0001c0001t0003g0138 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.210+7818A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21596121 | |||||||
| chr13:21596136 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(96): Show |
101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.210+7803G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21596136 | |||||||
| chr13:21596158 | A | C | 3 | a0001c0001t0003g0039 a0001c0001t0004g0182 a0001c0001t0004g0183 |
3 | HG00639.hp2 HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.210+7781T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21596158 | |||||||
| chr13:21596398 | C | T | 1 | a0001c0003t0003g0021 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.210+7541G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21596398 | |||||||
| chr13:21596429 | C | CT | 24 | a0001c0001t0001g0049 a0001c0003t0003g0003 a0001c0003t0003g0004 others(21): Show |
24 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.210+7509dupA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21596429 | |||||||
| chr13:21596429 | CT | C | 22 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(19): Show |
22 | HG01099.hp2 HG01192.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.210+7509delA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21596429 | |||||||
| chr13:21596510 | G | A | 33 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(30): Show |
33 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.210+7429C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21596510 | |||||||
| chr13:21596720 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.210+7219C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21596720 | |||||||
| chr13:21596734 | G | A | 10 | a0001c0001t0004g0212 a0001c0002t0005g0209 a0001c0002t0005g0210 others(7): Show |
10 | HG01099.hp2 HG01192.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.210+7205C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21596734 | |||||||
| chr13:21596739 | C | T | 21 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(18): Show |
21 | HG01099.hp2 HG01192.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.210+7200G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21596739 | |||||||
| chr13:21597019 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(92): Show |
97 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.210+6920T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597019 | |||||||
| chr13:21597175 | G | T | 1 | a0001c0001t0002g0222 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.210+6764C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597175 | |||||||
| chr13:21597304 | CTTAT | C | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+6631_210+6634d others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597304 | |||||||
| chr13:21597378 | T | C | 3 | a0001c0002t0001g0029 a0001c0002t0001g0034 a0001c0002t0001g0035 |
3 | HG02630.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.210+6561A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597378 | |||||||
| chr13:21597454 | C | G | 1 | a0001c0001t0003g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.210+6485G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597454 | |||||||
| chr13:21597492 | C | A | 92 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(89): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.210+6447G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597492 | |||||||
| chr13:21597637 | T | C | 6 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+6302A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597637 | |||||||
| chr13:21597649 | C | T | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02055.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.210+6290G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597649 | |||||||
| chr13:21597650 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(83): Show |
88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.210+6289C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597650 | |||||||
| chr13:21597653 | C | T | 22 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(19): Show |
22 | HG01099.hp2 HG01192.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.210+6286G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597653 | |||||||
| chr13:21597665 | T | C | 2 | a0001c0001t0003g0134 a0001c0001t0004g0141 |
2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.210+6274A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597665 | |||||||
| chr13:21597713 | C | T | 32 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(29): Show |
32 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.210+6226G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597713 | |||||||
| chr13:21597747 | C | T | 1 | a0001c0001t0003g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.210+6192G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597747 | |||||||
| chr13:21597751 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.210+6188C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597751 | |||||||
| chr13:21597822 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.210+6117A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597822 | |||||||
| chr13:21597930 | C | CA | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(239): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.210+6008dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597930 | |||||||
| chr13:21597930 | C | CAA | 26 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(23): Show |
26 | HG00423.hp1 HG01175.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.210+6007_210+6008d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597930 | |||||||
| chr13:21597930 | CAAAA | C | 13 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(10): Show |
13 | HG00639.hp2 HG00735.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.210+6005_210+6008d others(6): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597930 | |||||||
| chr13:21597948 | A | AC | 21 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(18): Show |
21 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.210+5990_210+5991i others(3): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597948 | |||||||
| chr13:21597970 | T | G | 1 | a0001c0001t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.210+5969A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21597970 | |||||||
| chr13:21598017 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.210+5922C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21598017 | |||||||
| chr13:21598029 | A | G | 21 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(18): Show |
21 | HG01099.hp2 HG01192.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.210+5910T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21598029 | |||||||
| chr13:21598063 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.210+5876T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21598063 | |||||||
| chr13:21598126 | G | A | 21 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(18): Show |
21 | HG01099.hp2 HG01192.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.210+5813C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21598126 | |||||||
| chr13:21598202 | C | G | 14 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.210+5737G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21598202 | |||||||
| chr13:21598486 | C | T | 33 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(30): Show |
33 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.210+5453G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21598486 | |||||||
| chr13:21598664 | C | T | 1 | a0001c0001t0003g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.210+5275G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21598664 | |||||||
| chr13:21598674 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.210+5265G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21598674 | |||||||
| chr13:21598798 | T | C | 1 | a0004c0009t0001g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.210+5141A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21598798 | |||||||
| chr13:21598883 | G | T | 8 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(5): Show |
8 | HG01243.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+5056C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21598883 | |||||||
| chr13:21599043 | C | T | 113 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(110): Show |
113 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.210+4896G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21599043 | |||||||
| chr13:21599101 | T | C | 1 | a0001c0001t0008g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.210+4838A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21599101 | |||||||
| chr13:21599162 | C | A | 1 | a0001c0001t0002g0296 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.210+4777G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21599162 | |||||||
| chr13:21599330 | A | C | 3 | a0001c0001t0003g0174 a0001c0001t0003g0177 a0001c0001t0008g0144 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.210+4609T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21599330 | |||||||
| chr13:21599398 | T | A | 113 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(110): Show |
113 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.210+4541A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21599398 | |||||||
| chr13:21599503 | T | C | 1 | a0001c0001t0002g0297 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.210+4436A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21599503 | |||||||
| chr13:21599564 | A | C | 113 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(110): Show |
113 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.210+4375T>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21599564 | |||||||
| chr13:21599587 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(257): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.210+4352T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21599587 | |||||||
| chr13:21599598 | A | T | 15 | a0001c0001t0003g0041 a0001c0001t0003g0042 a0001c0001t0003g0043 others(12): Show |
15 | HG00735.hp1 HG01074.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.210+4341T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21599598 | |||||||
| chr13:21599603 | T | C | 1 | a0001c0001t0002g0298 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.210+4336A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21599603 | |||||||
| chr13:21599656 | T | G | 113 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(110): Show |
113 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.210+4283A>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21599656 | |||||||
| chr13:21599952 | C | A | 113 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(110): Show |
113 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.210+3987G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21599952 | |||||||
| chr13:21600000 | A | G | 3 | a0001c0002t0006g0028 a0001c0002t0006g0181 a0001c0002t0006g0190 |
3 | HG00735.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.210+3939T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21600000 | |||||||
| chr13:21600010 | A | G | 8 | a0001c0001t0003g0039 a0001c0001t0003g0129 a0001c0001t0003g0130 others(5): Show |
8 | HG01243.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+3929T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21600010 | |||||||
| chr13:21600617 | A | G | 1 | a0001c0002t0001g0029 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.210+3322T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21600617 | |||||||
| chr13:21600628 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.210+3311C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21600628 | |||||||
| chr13:21600690 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG01081.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.210+3249A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21600690 | |||||||
| chr13:21600772 | T | C | 1 | a0001c0002t0001g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.210+3167A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21600772 | |||||||
| chr13:21600791 | C | T | 1 | a0001c0001t0002g0230 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.210+3148G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21600791 | |||||||
| chr13:21600793 | C | CTATTATT others(2): Show |
102 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(99): Show |
102 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.210+3137_210+3145d others(11): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21600793 | |||||||
| chr13:21600793 | C | CTATTATT others(5): Show |
6 | a0001c0001t0002g0233 a0001c0001t0002g0234 a0001c0001t0002g0235 others(3): Show |
6 | HG01069.hp1 HG01361.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+3134_210+3145d others(14): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21600793 | |||||||
| chr13:21600793 | C | CTATTATT others(8): Show |
2 | a0001c0001t0002g0231 a0001c0001t0002g0232 |
2 | NA19000.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.210+3131_210+3145d others(17): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21600793 | |||||||
| chr13:21600793 | C | T | 1 | a0001c0001t0002g0230 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.210+3146G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21600793 | |||||||
| chr13:21600812 | T | TATTATTA others(3): Show |
1 | a0001c0001t0002g0300 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.210+3126_210+3127i others(12): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21600812 | |||||||
| chr13:21600849 | T | C | 4 | a0001c0001t0002g0301 a0001c0001t0002g0302 a0001c0001t0002g0312 others(1): Show |
4 | HG01069.hp1 HG02572.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+3090A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21600849 | |||||||
| chr13:21600896 | A | T | 1 | a0001c0001t0001g0047 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.210+3043T>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21600896 | |||||||
| chr13:21600925 | T | C | 114 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(111): Show |
114 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.210+3014A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21600925 | |||||||
| chr13:21600997 | T | C | 1 | a0001c0001t0003g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.210+2942A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21600997 | |||||||
| chr13:21601143 | A | G | 11 | a0001c0001t0003g0192 a0001c0001t0004g0212 a0001c0002t0005g0209 others(8): Show |
11 | HG01099.hp2 HG01192.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.210+2796T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21601143 | |||||||
| chr13:21601299 | T | C | 9 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.210+2640A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21601299 | |||||||
| chr13:21601390 | T | C | 1 | a0001c0002t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.210+2549A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21601390 | |||||||
| chr13:21601554 | A | G | 30 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(27): Show |
30 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.210+2385T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21601554 | |||||||
| chr13:21601632 | GA | G | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(307): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.210+2306delT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21601632 | |||||||
| chr13:21601720 | G | C | 1 | a0001c0001t0001g0121 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.210+2219C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21601720 | |||||||
| chr13:21601754 | C | G | 18 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(15): Show |
18 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.210+2185G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21601754 | |||||||
| chr13:21601829 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.210+2110C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21601829 | |||||||
| chr13:21601833 | C | G | 7 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.210+2106G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21601833 | |||||||
| chr13:21601834 | TG | T | 7 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.210+2104delC | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21601834 | |||||||
| chr13:21601944 | C | A | 165 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(162): Show |
165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.210+1995G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21601944 | |||||||
| chr13:21602000 | T | C | 2 | a0001c0002t0005g0216 a0001c0002t0005g0217 |
2 | HG01192.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.210+1939A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602000 | |||||||
| chr13:21602011 | G | A | 23 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(20): Show |
23 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.210+1928C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602011 | |||||||
| chr13:21602042 | G | C | 1 | a0001c0001t0001g0123 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.210+1897C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602042 | |||||||
| chr13:21602104 | C | CA | 5 | a0001c0001t0001g0124 a0001c0001t0002g0221 a0001c0001t0002g0303 others(2): Show |
5 | NA18943.hp2 NA18956.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+1834dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602104 | |||||||
| chr13:21602104 | C | CAA | 24 | a0001c0001t0007g0306 a0001c0003t0003g0003 a0001c0003t0003g0004 others(21): Show |
24 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.210+1833_210+1834d others(4): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602104 | |||||||
| chr13:21602106 | AC | A | 33 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0202 others(30): Show |
33 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.210+1832delG | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602106 | |||||||
| chr13:21602107 | C | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(276): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.210+1832G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602107 | |||||||
| chr13:21602188 | A | G | 4 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(1): Show |
4 | HG01106.hp2 HG03704.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+1751T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602188 | |||||||
| chr13:21602248 | C | A | 1 | a0001c0002t0005g0218 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.210+1691G>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602248 | |||||||
| chr13:21602297 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(83): Show |
88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.210+1642G>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602297 | |||||||
| chr13:21602380 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.210+1559C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602380 | |||||||
| chr13:21602466 | A | G | 8 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(5): Show |
8 | HG00733.hp2 HG01175.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+1473T>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602466 | |||||||
| chr13:21602520 | C | CA | 65 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(62): Show |
65 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.210+1418dupT | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602520 | |||||||
| chr13:21602574 | G | A | 1 | a0001c0001t0003g0192 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.210+1365C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602574 | |||||||
| chr13:21602615 | C | G | 18 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0005 others(15): Show |
18 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.210+1324G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602615 | |||||||
| chr13:21602687 | T | C | 4 | a0001c0001t0004g0186 a0001c0001t0004g0187 a0001c0001t0004g0188 others(1): Show |
4 | HG01891.hp1 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+1252A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602687 | |||||||
| chr13:21602706 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.210+1233A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602706 | |||||||
| chr13:21602723 | C | G | 1 | a0001c0001t0003g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.210+1216G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602723 | |||||||
| chr13:21602786 | T | C | 1 | a0001c0002t0006g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.210+1153A>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602786 | |||||||
| chr13:21602813 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.210+1126C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602813 | |||||||
| chr13:21602969 | CT | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(171): Show |
176 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.210+969delA | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602969 | |||||||
| chr13:21602969 | CTT | C | 115 | a0001c0001t0001g0176 a0001c0001t0001g0201 a0001c0001t0001g0202 others(112): Show |
115 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.210+968_210+969del others(2): Show |
MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21602969 | |||||||
| chr13:21603093 | C | G | 11 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.210+846G>C | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21603093 | |||||||
| chr13:21603094 | G | A | 14 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.210+845C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21603094 | |||||||
| chr13:21603208 | G | C | 9 | a0001c0001t0003g0191 a0001c0001t0003g0192 a0001c0001t0003g0193 others(6): Show |
9 | HG00735.hp1 HG01074.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.210+731C>G | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21603208 | |||||||
| chr13:21603252 | G | T | 1 | a0001c0002t0006g0028 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.210+687C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21603252 | |||||||
| chr13:21603271 | G | A | 113 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(110): Show |
113 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.210+668C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21603271 | |||||||
| chr13:21603319 | G | A | 2 | a0001c0001t0002g0312 a0001c0001t0002g0313 |
2 | HG01069.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.210+620C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21603319 | |||||||
| chr13:21603532 | T | A | 10 | a0001c0001t0004g0212 a0001c0002t0005g0209 a0001c0002t0005g0210 others(7): Show |
10 | HG01099.hp2 HG01192.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.210+407A>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21603532 | |||||||
| chr13:21603780 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.210+159C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21603780 | |||||||
| chr13:21603819 | G | A | 1 | a0003c0007t0001g0219 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.210+120C>T | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21603819 | |||||||
| chr13:21603906 | G | T | 1 | a0001c0001t0003g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.210+33C>A | MICU2 | ENSG00000165487.14 | transcript | ENST00000382374.9 | protein_coding | 1/11 | chr13 | 21603906 |