Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23209 |
| ensemblid | ENSG00000100427.16 |
| hgncid | 17082 |
| symbol | MLC1 |
| name | modulator of VRAC current 1 |
| refseq_nuc | NM_015166.4 |
| refseq_prot | NP_055981.1 |
| ensembl_nuc | ENST00000311597.10 |
| ensembl_prot | ENSP00000310375.6 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 50059391 |
| end | 50085426 |
| strand | - |
| ver | v1.2 |
| region | chr22:50059391-50085426 |
| region5000 | chr22:50054391-50090426 |
| regionname0 | MLC1_chr22_50059391_50085426 |
| regionname5000 | MLC1_chr22_50054391_50090426 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 377 | 202 | 46 | 45 | 85 | 8 | 16 | 62 | MLC1_chr22_50054391_50090426 | MLC1 | MTQEP others(372): Show |
chr22 | 50054391 | 50090426 |
| a0002 | 0/0 | 388 | 4 | 0 | 2 | 1 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | MTQEP others(383): Show |
chr22 | 50054391 | 50090426 |
| a0003 | 0/0 | 377 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | MTQEP others(372): Show |
chr22 | 50054391 | 50090426 |
| a0004 | 0/0 | 377 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | MTQEP others(372): Show |
chr22 | 50054391 | 50090426 |
| a0005 | 0/0 | 369 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | MTQEP others(364): Show |
chr22 | 50054391 | 50090426 |
| a0006 | 0/0 | 377 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | MTQEP others(372): Show |
chr22 | 50054391 | 50090426 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1131 | 198 | 45 | 44 | 84 | 8 | 15 | MLC1_chr22_50054391_50090426 | MLC1 | ATGAC others(1126): Show |
chr22 | 50054391 | 50090426 | ||
| a0001c0005 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATGAC others(1126): Show |
chr22 | 50054391 | 50090426 | ||
| a0001c0007 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATGAC others(1126): Show |
chr22 | 50054391 | 50090426 | ||
| a0001c0009 | 0/0 | 1131 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATGAC others(1126): Show |
chr22 | 50054391 | 50090426 | ||
| a0001c0010 | 0/0 | 1131 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | ATGAC others(1126): Show |
chr22 | 50054391 | 50090426 | ||
| a0002c0002 | 0/0 | 1164 | 4 | 0 | 2 | 1 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | ATGAC others(1159): Show |
chr22 | 50054391 | 50090426 | ||
| a0003c0003 | 0/0 | 1131 | 2 | 1 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATGAC others(1126): Show |
chr22 | 50054391 | 50090426 | ||
| a0004c0004 | 0/0 | 1131 | 2 | 1 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATGAC others(1126): Show |
chr22 | 50054391 | 50090426 | ||
| a0005c0008 | 0/0 | 1163 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | ATGAC others(1158): Show |
chr22 | 50054391 | 50090426 | ||
| a0006c0006 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATGAC others(1126): Show |
chr22 | 50054391 | 50090426 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3457 | 89 | 29 | 6 | 46 | 1 | 5 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0002 | 0/0 | 3457 | 48 | 0 | 9 | 32 | 3 | 4 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0003 | 0/0 | 3457 | 14 | 1 | 9 | 0 | 1 | 3 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0004 | 0/0 | 3457 | 8 | 0 | 4 | 0 | 2 | 2 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0005 | 0/0 | 3457 | 7 | 6 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0006 | 0/0 | 3457 | 7 | 1 | 5 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0007 | 0/0 | 3457 | 5 | 0 | 3 | 0 | 1 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0009 | 0/0 | 3457 | 4 | 3 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0010 | 0/0 | 3459 | 2 | 0 | 2 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3454): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0011 | 0/0 | 3457 | 2 | 2 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0012 | 0/0 | 3457 | 2 | 0 | 2 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0013 | 0/0 | 3457 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0015 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0016 | 0/0 | 3458 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3453): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0017 | 0/0 | 3457 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0018 | 0/0 | 3458 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3453): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0019 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0020 | 0/0 | 3457 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0022 | 0/0 | 3457 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0023 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0001t0024 | 0/0 | 3457 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0005t0013 | 0/0 | 3457 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0007t0001 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0009t0014 | 0/0 | 3457 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0001c0010t0001 | 0/0 | 3457 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0002c0002t0008 | 0/0 | 3396 | 4 | 0 | 2 | 1 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3391): Show |
chr22 | 50054391 | 50090426 |
| a0003c0003t0001 | 0/0 | 3457 | 2 | 1 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0004c0004t0004 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0004c0004t0021 | 0/0 | 3457 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| a0005c0008t0008 | 0/0 | 3395 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3390): Show |
chr22 | 50054391 | 50090426 |
| a0006c0006t0002 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | ATTTG others(3452): Show |
chr22 | 50054391 | 50090426 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0005g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0005g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0006g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0007g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0007g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0009g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0010g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0011g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0011g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0012g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0012g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0013g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0015g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0016g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0017g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0018g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0019g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0020g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0022g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0023g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0001t0024g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0005t0013g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0007t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0009t0014g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0001c0010t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0002c0002t0008g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0002c0002t0008g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0002c0002t0008g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0002c0002t0008g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0003c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0003c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0004c0004t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0004c0004t0021g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0005c0008t0008g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| a0006c0006t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0056 | EUR | GBR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | CHS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG00438 | hp2 | a0001 | c0001 | t0019 | g0021 | EAS | CHS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG00621 | hp1 | a0001 | c0001 | t0006 | g0112 | EAS | CHS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG00673 | hp1 | a0002 | c0002 | t0008 | g0168 | EAS | CHS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG00733 | hp2 | a0001 | c0001 | t0012 | g0116 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0174 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0187 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0068 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0029 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01192 | hp2 | a0001 | c0001 | t0007 | g0061 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01243 | hp1 | a0001 | c0001 | t0013 | g0089 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01255 | hp2 | a0001 | c0001 | t0009 | g0011 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01256 | hp2 | a0001 | c0001 | t0022 | g0098 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0055 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01358 | hp1 | a0002 | c0002 | t0008 | g0167 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0111 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0181 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0179 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01496 | hp2 | a0001 | c0009 | t0014 | g0105 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01515 | hp1 | a0001 | c0001 | t0007 | g0109 | EUR | IBS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0180 | EUR | IBS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01975 | hp2 | a0001 | c0001 | t0006 | g0118 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02004 | hp1 | a0002 | c0002 | t0008 | g0166 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02004 | hp2 | a0001 | c0001 | t0010 | g0014 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02074 | hp1 | a0001 | c0001 | t0018 | g0091 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02148 | hp2 | a0001 | c0001 | t0012 | g0108 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02257 | hp1 | a0001 | c0001 | t0024 | g0190 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02273 | hp1 | a0001 | c0001 | t0010 | g0014 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02273 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0115 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02622 | hp2 | a0001 | c0005 | t0013 | g0064 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0066 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0011 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02965 | hp1 | a0001 | c0001 | t0017 | g0082 | AFR | ESN | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0088 | AFR | MSL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0030 | AFR | MSL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03239 | hp1 | a0001 | c0001 | t0007 | g0049 | SAS | PJL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0173 | SAS | PJL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0183 | SAS | PJL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03688 | hp1 | a0002 | c0002 | t0008 | g0165 | SAS | STU | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03688 | hp2 | a0001 | c0010 | t0001 | g0132 | SAS | STU | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0175 | SAS | PJL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0176 | SAS | PJL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03831 | hp1 | a0005 | c0008 | t0008 | g0119 | SAS | BEB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | BEB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0178 | SAS | BEB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | YRI | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18967 | hp2 | a0001 | c0001 | t0015 | g0020 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18978 | hp1 | a0001 | c0001 | t0023 | g0145 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19043 | hp1 | a0001 | c0001 | t0020 | g0189 | AFR | LWK | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19065 | hp1 | a0001 | c0007 | t0001 | g0054 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19074 | hp1 | a0006 | c0006 | t0002 | g0157 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19087 | hp1 | a0004 | c0004 | t0004 | g0164 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA19090 | hp2 | a0001 | c0001 | t0016 | g0107 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA20129 | hp1 | a0001 | c0001 | t0009 | g0078 | AFR | ASW | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0160 | EUR | TSI | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0113 | EUR | TSI | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0170 | EUR | TSI | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG02486 | hp2 | a0001 | c0001 | t0011 | g0081 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| HG03471 | hp2 | a0004 | c0004 | t0021 | g0163 | AFR | MSL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | USA | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0110 | AFR | USA | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0063 | REF | REF | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0101 | REF | REF | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:50061603 | C | T | 1 | a0006 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.1114G>A | p.Val372Met | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1245/3457 | 1114/1134 | 372/377 | chr22 | 50061603 | |||
| chr22:50064040 | A | AGCACCCC others(25): Show |
1 | a0005 | 1 | HG03831.hp1 | frameshift_variant | HIGH | c.1052_1053insCGGGGA others(26): Show |
p.Ala355fs | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/12 | 1183/3457 | 1052/1134 | 351/377 | chr22 | 50064040 | |||
| chr22:50064040 | A | AGCACCCC others(26): Show |
1 | a0002 | 4 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(1): Show |
disruptive_inframe_insertion | MODERATE | c.1052_1053insCGGGGA others(27): Show |
p.Ala351_Gly352insGl others(31): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/12 | 1183/3457 | 1052/1134 | 351/377 | chr22 | 50064040 | |||
| chr22:50064062 | T | C | 2 | a0002 a0005 |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
missense_variant | MODERATE | c.1031A>G | p.Asn344Ser | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/12 | 1162/3457 | 1031/1134 | 344/377 | chr22 | 50064062 | |||
| chr22:50064161 | A | T | 1 | a0003 | 2 | HG01109.hp1 HG02630.hp1 |
missense_variant | MODERATE | c.932T>A | p.Val311Glu | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/12 | 1063/3457 | 932/1134 | 311/377 | chr22 | 50064161 | |||
| chr22:50077414 | C | A | 2 | a0002 a0004 |
6 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(3): Show |
missense_variant | MODERATE | c.512G>T | p.Cys171Phe | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 6/12 | 643/3457 | 512/1134 | 171/377 | chr22 | 50077414 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:50064088 | C | A | 1 | a0001c0007 | 1 | NA19065.hp1 | synonymous_variant | LOW | c.1005G>T | p.Leu335Leu | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/12 | 1136/3457 | 1005/1134 | 335/377 | chr22 | 50064088 | |||
| chr22:50064097 | A | G | 2 | a0002c0002 a0005c0008 |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
synonymous_variant | LOW | c.996T>C | p.Ser332Ser | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/12 | 1127/3457 | 996/1134 | 332/377 | chr22 | 50064097 | |||
| chr22:50064115 | G | A | 2 | a0002c0002 a0005c0008 |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
synonymous_variant | LOW | c.978C>T | p.Cys326Cys | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/12 | 1109/3457 | 978/1134 | 326/377 | chr22 | 50064115 | |||
| chr22:50076841 | T | C | 3 | a0001c0009 a0002c0002 a0004c0004 |
7 | HG00673.hp1 HG01358.hp1 HG01496.hp2 others(4): Show |
splice_region_variant&synonymous_variant | LOW | c.597A>G | p.Ser199Ser | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/12 | 728/3457 | 597/1134 | 199/377 | chr22 | 50076841 | |||
| chr22:50076844 | G | A | 3 | a0001c0009 a0002c0002 a0004c0004 |
7 | HG00673.hp1 HG01358.hp1 HG01496.hp2 others(4): Show |
synonymous_variant | LOW | c.594C>T | p.Tyr198Tyr | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/12 | 725/3457 | 594/1134 | 198/377 | chr22 | 50076844 | |||
| chr22:50076895 | G | A | 1 | a0001c0010 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.543C>T | p.Ser181Ser | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/12 | 674/3457 | 543/1134 | 181/377 | chr22 | 50076895 | |||
| chr22:50083135 | C | T | 1 | a0001c0005 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.216G>A | p.Leu72Leu | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/12 | 347/3457 | 216/1134 | 72/377 | chr22 | 50083135 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:50059532 | C | T | 1 | a0001c0001t0023 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2051G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 2051 | chr22 | 50059532 | ||||||
| chr22:50059533 | G | A | 1 | a0001c0001t0017 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2050C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 2050 | chr22 | 50059533 | ||||||
| chr22:50059601 | G | GC | 4 | a0001c0001t0010 a0001c0001t0018 a0002c0002t0008 others(1): Show |
8 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1981dupG | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1981 | chr22 | 50059601 | ||||||
| chr22:50059620 | G | C | 1 | a0001c0001t0007 | 5 | HG01175.hp1 HG01192.hp2 HG01346.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1963C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1963 | chr22 | 50059620 | ||||||
| chr22:50059747 | C | T | 1 | a0001c0001t0012 | 2 | HG00733.hp2 HG02148.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1836G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1836 | chr22 | 50059747 | ||||||
| chr22:50059819 | C | A | 2 | a0001c0001t0004 a0004c0004t0004 |
9 | HG00099.hp1 HG00741.hp1 HG01106.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1764G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1764 | chr22 | 50059819 | ||||||
| chr22:50059894 | A | C | 1 | a0001c0001t0011 | 2 | HG02486.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1689T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1689 | chr22 | 50059894 | ||||||
| chr22:50059960 | C | A | 4 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0013 others(1): Show |
8 | HG00733.hp2 HG01243.hp1 HG01255.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1623G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1623 | chr22 | 50059960 | ||||||
| chr22:50060214 | A | AT | 2 | a0001c0001t0010 a0001c0001t0016 |
3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1368dupA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1368 | chr22 | 50060214 | ||||||
| chr22:50060249 | C | T | 2 | a0001c0001t0010 a0001c0001t0016 |
3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1334G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1334 | chr22 | 50060249 | ||||||
| chr22:50060262 | T | C | 1 | a0001c0009t0014 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1321A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1321 | chr22 | 50060262 | ||||||
| chr22:50060440 | G | A | 3 | a0001c0001t0010 a0001c0001t0016 a0001c0009t0014 |
4 | HG01496.hp2 HG02004.hp2 HG02273.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1143C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1143 | chr22 | 50060440 | ||||||
| chr22:50060456 | G | A | 3 | a0001c0001t0003 a0001c0001t0004 a0004c0004t0004 |
23 | HG00099.hp1 HG00741.hp1 HG01070.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1127C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1127 | chr22 | 50060456 | ||||||
| chr22:50060592 | A | C | 2 | a0002c0002t0008 a0005c0008t0008 |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*991T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 991 | chr22 | 50060592 | ||||||
| chr22:50060613 | C | G | 2 | a0001c0001t0010 a0001c0001t0016 |
3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*970G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 970 | chr22 | 50060613 | ||||||
| chr22:50060646 | G | A | 2 | a0002c0002t0008 a0005c0008t0008 |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*937C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 937 | chr22 | 50060646 | ||||||
| chr22:50060697 | AGCAGCGG others(95): Show |
A | 2 | a0002c0002t0008 a0005c0008t0008 |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*784_*885del | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 784 | chr22 | 50060697 | ||||||
| chr22:50060736 | G | T | 1 | a0001c0001t0007 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*847C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 847 | chr22 | 50060736 | ||||||
| chr22:50060759 | TGTGGCAC others(44): Show |
T | 7 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0012 others(4): Show |
12 | HG00733.hp2 HG01243.hp1 HG01255.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*773_*823delGTGGCC others(45): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 773 | chr22 | 50060759 | ||||||
| chr22:50060910 | C | T | 1 | a0001c0001t0020 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*673G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 673 | chr22 | 50060910 | ||||||
| chr22:50060922 | C | G | 1 | a0001c0001t0009 | 4 | HG01255.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*661G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 661 | chr22 | 50060922 | ||||||
| chr22:50061011 | G | A | 1 | a0001c0009t0014 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*572C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 572 | chr22 | 50061011 | ||||||
| chr22:50061031 | A | T | 1 | a0001c0001t0015 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*552T>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 552 | chr22 | 50061031 | ||||||
| chr22:50061063 | G | A | 1 | a0001c0001t0019 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*520C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 520 | chr22 | 50061063 | ||||||
| chr22:50061152 | G | A | 2 | a0001c0001t0020 a0004c0004t0021 |
2 | HG03471.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*431C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 431 | chr22 | 50061152 | ||||||
| chr22:50061169 | G | A | 1 | a0001c0001t0006 | 7 | HG00621.hp1 HG01358.hp2 HG01975.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*414C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 414 | chr22 | 50061169 | ||||||
| chr22:50061205 | T | TGACCCCC | 2 | a0002c0002t0008 a0005c0008t0008 |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*377_*378insGGGGGT others(1): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 377 | chr22 | 50061205 | ||||||
| chr22:50061244 | G | A | 1 | a0001c0001t0005 | 7 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*339C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 339 | chr22 | 50061244 | ||||||
| chr22:50061528 | G | A | 1 | a0001c0001t0022 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*55C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 55 | chr22 | 50061528 | ||||||
| chr22:50061535 | T | C | 6 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0023 others(3): Show |
62 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*48A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 48 | chr22 | 50061535 | ||||||
| chr22:50061538 | T | C | 4 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0013 others(1): Show |
8 | HG00733.hp2 HG01243.hp1 HG01255.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*45A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 45 | chr22 | 50061538 | ||||||
| chr22:50061571 | C | T | 1 | a0001c0009t0014 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 12 | chr22 | 50061571 | ||||||
| chr22:50085395 | T | C | 1 | a0001c0001t0024 | 1 | HG02257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-100A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 1/12 | 493 | chr22 | 50085395 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:50061834 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-177A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50061834 | |||||||
| chr22:50061868 | C | T | 1 | a0001c0001t0002g0153 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1060-211G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50061868 | |||||||
| chr22:50061872 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1060-215G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50061872 | |||||||
| chr22:50061928 | G | C | 1 | a0001c0001t0010g0014 | 2 | HG02004.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1060-271C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50061928 | |||||||
| chr22:50061938 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1060-281G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50061938 | |||||||
| chr22:50061946 | G | T | 2 | a0001c0001t0001g0023 a0001c0001t0015g0020 |
2 | NA18967.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1060-289C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50061946 | |||||||
| chr22:50062046 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0084 a0001c0001t0001g0086 |
4 | HG02965.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-389C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062046 | |||||||
| chr22:50062098 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-441A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062098 | |||||||
| chr22:50062125 | C | T | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-468G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062125 | |||||||
| chr22:50062171 | A | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-514T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062171 | |||||||
| chr22:50062172 | C | T | 2 | a0001c0001t0010g0014 a0001c0001t0016g0107 |
3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1060-515G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062172 | |||||||
| chr22:50062176 | A | AAGCCCCA others(13): Show |
2 | a0001c0001t0001g0023 a0001c0001t0015g0020 |
2 | NA18967.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1060-539_1060-520d others(22): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062176 | |||||||
| chr22:50062176 | A | G | 1 | a0001c0009t0014g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1060-519T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062176 | |||||||
| chr22:50062187 | ATCCACCC others(13): Show |
A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0031 others(10): Show |
16 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1060-550_1060-531d others(22): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062187 | |||||||
| chr22:50062188 | T | TCCACCCT others(13): Show |
1 | a0004c0004t0021g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1060-532_1060-531i others(22): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062188 | |||||||
| chr22:50062188 | T | TCCACCCT others(33): Show |
1 | a0001c0001t0020g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1060-532_1060-531i others(42): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062188 | |||||||
| chr22:50062208 | T | C | 152 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(149): Show |
169 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.1060-551A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062208 | |||||||
| chr22:50062208 | T | TCCACCCT others(121): Show |
18 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0084 others(15): Show |
20 | HG00544.hp1 HG01256.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1060-552_1060-551i others(130): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062208 | |||||||
| chr22:50062222 | C | CAGCCGCC others(33): Show |
5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-566_1060-565i others(42): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062222 | |||||||
| chr22:50062244 | A | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-587T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062244 | |||||||
| chr22:50062267 | A | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-610T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062267 | |||||||
| chr22:50062268 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1060-611G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062268 | |||||||
| chr22:50062274 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-617A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062274 | |||||||
| chr22:50062279 | C | A | 49 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
53 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.1060-622G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062279 | |||||||
| chr22:50062288 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-631A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062288 | |||||||
| chr22:50062292 | T | C | 6 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(3): Show |
6 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-635A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062292 | |||||||
| chr22:50062292 | TCCTGAGC others(13): Show |
T | 1 | a0001c0001t0002g0159 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1060-655_1060-636d others(22): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062292 | |||||||
| chr22:50062522 | AACAGCAG others(37): Show |
A | 1 | a0001c0001t0002g0143 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1060-909_1060-866d others(46): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062522 | |||||||
| chr22:50062615 | T | C | 1 | a0001c0001t0002g0143 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1060-958A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062615 | |||||||
| chr22:50062617 | G | C | 1 | a0001c0001t0002g0143 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1060-960C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062617 | |||||||
| chr22:50062630 | A | G | 97 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0031 others(94): Show |
111 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.1060-973T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062630 | |||||||
| chr22:50062677 | C | A | 1 | a0001c0001t0002g0143 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1060-1020G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062677 | |||||||
| chr22:50062678 | A | G | 1 | a0001c0001t0002g0143 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1060-1021T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062678 | |||||||
| chr22:50062681 | G | C | 1 | a0001c0001t0002g0143 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1060-1024C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062681 | |||||||
| chr22:50062708 | A | G | 7 | a0001c0001t0010g0014 a0001c0001t0016g0107 a0002c0002t0008g0165 others(4): Show |
8 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1060-1051T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062708 | |||||||
| chr22:50062791 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-1134G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062791 | |||||||
| chr22:50062805 | G | T | 1 | a0001c0005t0013g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1060-1148C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062805 | |||||||
| chr22:50062810 | C | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0041 |
2 | NA18947.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1060-1153G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062810 | |||||||
| chr22:50062811 | G | A | 1 | a0003c0003t0001g0066 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1060-1154C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062811 | |||||||
| chr22:50062845 | C | T | 2 | a0001c0001t0002g0129 a0001c0001t0002g0148 |
2 | HG02602.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1060-1188G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062845 | |||||||
| chr22:50062852 | C | T | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+1182G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062852 | |||||||
| chr22:50062918 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1059+1116G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062918 | |||||||
| chr22:50062975 | G | A | 1 | a0001c0001t0002g0152 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1059+1059C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062975 | |||||||
| chr22:50063056 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+978C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063056 | |||||||
| chr22:50063111 | A | AAGCGTTA others(7): Show |
1 | a0005c0008t0008g0119 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1059+922_1059+923i others(16): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063111 | |||||||
| chr22:50063115 | A | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+919T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063115 | |||||||
| chr22:50063157 | C | T | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+877G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063157 | |||||||
| chr22:50063201 | G | T | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+833C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063201 | |||||||
| chr22:50063256 | T | C | 170 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(167): Show |
190 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.1059+778A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063256 | |||||||
| chr22:50063366 | G | A | 1 | a0001c0001t0012g0116 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1059+668C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063366 | |||||||
| chr22:50063405 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+629C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063405 | |||||||
| chr22:50063458 | C | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+576G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063458 | |||||||
| chr22:50063459 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+575A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063459 | |||||||
| chr22:50063472 | C | CA | 6 | a0001c0001t0001g0045 a0001c0001t0002g0143 a0001c0001t0002g0144 others(3): Show |
6 | HG01496.hp2 NA18963.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1059+561dupT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063472 | |||||||
| chr22:50063472 | CA | C | 9 | a0001c0001t0001g0046 a0001c0001t0001g0058 a0001c0001t0001g0083 others(6): Show |
9 | HG01070.hp2 HG01256.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.1059+561delT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063472 | |||||||
| chr22:50063472 | CAAAAA | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+557_1059+561d others(7): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063472 | |||||||
| chr22:50063490 | A | AC | 1 | a0001c0001t0010g0014 | 2 | HG02004.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1059+543_1059+544i others(3): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063490 | |||||||
| chr22:50063490 | A | C | 1 | a0001c0001t0016g0107 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1059+544T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063490 | |||||||
| chr22:50063496 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+538C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063496 | |||||||
| chr22:50063511 | T | G | 2 | a0001c0001t0010g0014 a0001c0001t0016g0107 |
3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1059+523A>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063511 | |||||||
| chr22:50063528 | G | C | 21 | a0001c0001t0003g0004 a0001c0001t0003g0169 a0001c0001t0003g0170 others(18): Show |
23 | HG00099.hp1 HG00741.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1059+506C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063528 | |||||||
| chr22:50063587 | C | A | 1 | a0001c0001t0004g0180 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1059+447G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063587 | |||||||
| chr22:50063621 | G | GCAGGCCT others(60): Show |
1 | a0001c0001t0007g0029 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1059+346_1059+412d others(69): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063621 | |||||||
| chr22:50063706 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+328A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063706 | |||||||
| chr22:50063730 | T | G | 1 | a0001c0001t0001g0023 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1059+304A>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063730 | |||||||
| chr22:50063742 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+292A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063742 | |||||||
| chr22:50063743 | G | GACCA | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+290_1059+291i others(6): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063743 | |||||||
| chr22:50063772 | T | TGGCTGGG others(94): Show |
2 | a0001c0001t0020g0189 a0004c0004t0021g0163 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1059+261_1059+262i others(103): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063772 | |||||||
| chr22:50063781 | C | A | 2 | a0001c0001t0020g0189 a0004c0004t0021g0163 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1059+253G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063781 | |||||||
| chr22:50063781 | C | CCCCCCAT others(226): Show |
1 | a0001c0001t0002g0143 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1059+252_1059+253i others(235): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063781 | |||||||
| chr22:50063786 | A | ATGGGCCA others(223): Show |
1 | a0001c0001t0001g0060 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1059+247_1059+248i others(232): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063786 | |||||||
| chr22:50063786 | A | ATGGGCCA others(222): Show |
1 | a0001c0001t0001g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1059+247_1059+248i others(231): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063786 | |||||||
| chr22:50063786 | A | ATGGGCCA others(223): Show |
174 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
196 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.1059+247_1059+248i others(232): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063786 | |||||||
| chr22:50063786 | A | ATGGGCCA others(224): Show |
1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1059+247_1059+248i others(233): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063786 | |||||||
| chr22:50063786 | A | G | 8 | a0001c0001t0002g0143 a0001c0001t0020g0189 a0002c0002t0008g0165 others(5): Show |
8 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+248T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063786 | |||||||
| chr22:50063814 | A | ACTGCAGG others(160): Show |
5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+219_1059+220i others(169): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063814 | |||||||
| chr22:50063817 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+217C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063817 | |||||||
| chr22:50063832 | C | CCCCAGCT others(222): Show |
1 | a0001c0001t0001g0045 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1059+201_1059+202i others(231): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063832 | |||||||
| chr22:50063836 | G | A | 3 | a0001c0001t0001g0103 a0001c0001t0004g0176 a0001c0001t0004g0181 |
3 | HG01433.hp1 HG02486.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1059+198C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063836 | |||||||
| chr22:50063856 | T | C | 2 | a0001c0001t0004g0176 a0001c0001t0004g0181 |
2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1059+178A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063856 | |||||||
| chr22:50063872 | A | G | 2 | a0001c0001t0004g0176 a0001c0001t0004g0181 |
2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1059+162T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063872 | |||||||
| chr22:50063878 | T | A | 2 | a0001c0001t0004g0176 a0001c0001t0004g0181 |
2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1059+156A>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063878 | |||||||
| chr22:50063882 | C | CACAGGCT others(155): Show |
2 | a0001c0001t0004g0176 a0001c0001t0004g0181 |
2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1059+151_1059+152i others(164): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063882 | |||||||
| chr22:50063884 | T | C | 2 | a0001c0001t0004g0176 a0001c0001t0004g0181 |
2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1059+150A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063884 | |||||||
| chr22:50063920 | G | GGGCTACT others(28): Show |
2 | a0001c0001t0004g0176 a0001c0001t0004g0181 |
2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1059+113_1059+114i others(37): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063920 | |||||||
| chr22:50064007 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+27A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50064007 | |||||||
| chr22:50064018 | C | T | 50 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
54 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1059+16G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50064018 | |||||||
| chr22:50064206 | C | T | 1 | a0001c0001t0002g0128 | 1 | NA19056.hp1 | splice_region_variant&intron_variant | LOW | c.895-8G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064206 | |||||||
| chr22:50064207 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-9C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064207 | |||||||
| chr22:50064221 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-23C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064221 | |||||||
| chr22:50064337 | C | T | 12 | a0001c0001t0009g0011 a0001c0001t0009g0078 a0001c0001t0009g0088 others(9): Show |
13 | HG00673.hp1 HG00733.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.895-139G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064337 | |||||||
| chr22:50064383 | T | C | 1 | a0001c0009t0014g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.895-185A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064383 | |||||||
| chr22:50064457 | C | T | 81 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(78): Show |
88 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.895-259G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064457 | |||||||
| chr22:50064459 | T | C | 50 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
54 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.895-261A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064459 | |||||||
| chr22:50064464 | A | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0031 others(10): Show |
16 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.895-266T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064464 | |||||||
| chr22:50064492 | C | G | 1 | a0001c0009t0014g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.895-294G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064492 | |||||||
| chr22:50064571 | G | A | 2 | a0001c0001t0010g0014 a0001c0001t0016g0107 |
3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.895-373C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064571 | |||||||
| chr22:50064622 | G | A | 1 | a0001c0009t0014g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.895-424C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064622 | |||||||
| chr22:50064632 | GT | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-435delA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064632 | |||||||
| chr22:50064634 | G | T | 2 | a0001c0001t0010g0014 a0001c0001t0016g0107 |
3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.895-436C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064634 | |||||||
| chr22:50064883 | CA | C | 21 | a0001c0001t0003g0004 a0001c0001t0003g0169 a0001c0001t0003g0170 others(18): Show |
23 | HG00099.hp1 HG00741.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.895-686delT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064883 | |||||||
| chr22:50064907 | C | A | 6 | a0001c0001t0009g0011 a0001c0001t0009g0078 a0001c0001t0009g0088 others(3): Show |
7 | HG00733.hp2 HG01255.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.895-709G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064907 | |||||||
| chr22:50064907 | C | T | 53 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(50): Show |
57 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.895-709G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064907 | |||||||
| chr22:50064930 | A | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-732T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064930 | |||||||
| chr22:50064949 | C | CAG | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-753_895-752dup others(2): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064949 | |||||||
| chr22:50065212 | C | G | 13 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0031 others(10): Show |
16 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.895-1014G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065212 | |||||||
| chr22:50065215 | G | A | 2 | a0001c0001t0020g0189 a0004c0004t0021g0163 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.895-1017C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065215 | |||||||
| chr22:50065368 | C | CA | 6 | a0001c0001t0001g0026 a0001c0001t0001g0065 a0001c0001t0009g0011 others(3): Show |
7 | HG01255.hp2 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.895-1171dupT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065368 | |||||||
| chr22:50065368 | CAA | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-1172_895-1171d others(4): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065368 | |||||||
| chr22:50065411 | C | T | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-1213G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065411 | |||||||
| chr22:50065635 | A | G | 6 | a0001c0001t0009g0011 a0001c0001t0009g0078 a0001c0001t0009g0088 others(3): Show |
7 | HG00733.hp2 HG01255.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.895-1437T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065635 | |||||||
| chr22:50065650 | C | T | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-1452G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065650 | |||||||
| chr22:50065725 | T | C | 2 | a0001c0001t0020g0189 a0004c0004t0021g0163 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.895-1527A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065725 | |||||||
| chr22:50065881 | C | T | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-1683G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065881 | |||||||
| chr22:50065938 | G | T | 1 | a0001c0001t0001g0057 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.895-1740C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065938 | |||||||
| chr22:50066017 | A | G | 170 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(167): Show |
190 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.895-1819T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066017 | |||||||
| chr22:50066058 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-1860A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066058 | |||||||
| chr22:50066078 | TC | T | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-1881delG | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066078 | |||||||
| chr22:50066118 | G | T | 1 | a0002c0002t0008g0165 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.895-1920C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066118 | |||||||
| chr22:50066208 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-2010C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066208 | |||||||
| chr22:50066242 | T | C | 1 | a0004c0004t0021g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.895-2044A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066242 | |||||||
| chr22:50066257 | G | A | 50 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
54 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.895-2059C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066257 | |||||||
| chr22:50066274 | G | A | 9 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0080 others(6): Show |
12 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.895-2076C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066274 | |||||||
| chr22:50066308 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-2110C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066308 | |||||||
| chr22:50066312 | A | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-2114T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066312 | |||||||
| chr22:50066352 | A | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+2081T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066352 | |||||||
| chr22:50066375 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+2058A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066375 | |||||||
| chr22:50066478 | A | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+1955T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066478 | |||||||
| chr22:50066524 | T | G | 170 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(167): Show |
190 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.894+1909A>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066524 | |||||||
| chr22:50066659 | T | TA | 9 | a0001c0001t0001g0058 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
10 | HG01255.hp2 HG01358.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.894+1773dupT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066659 | |||||||
| chr22:50066702 | T | C | 1 | a0001c0001t0003g0184 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.894+1731A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066702 | |||||||
| chr22:50066704 | C | G | 21 | a0001c0001t0003g0004 a0001c0001t0003g0169 a0001c0001t0003g0170 others(18): Show |
23 | HG00099.hp1 HG00741.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.894+1729G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066704 | |||||||
| chr22:50066723 | G | GA | 6 | a0001c0001t0002g0124 a0001c0001t0002g0134 a0001c0001t0002g0135 others(3): Show |
6 | HG02148.hp1 NA18946.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.894+1709dupT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066723 | |||||||
| chr22:50066754 | GAGGAGCA others(8): Show |
G | 1 | a0001c0001t0001g0096 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.894+1664_894+1678d others(17): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066754 | |||||||
| chr22:50066858 | T | C | 1 | a0001c0001t0002g0150 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.894+1575A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066858 | |||||||
| chr22:50066860 | T | TA | 7 | a0001c0001t0002g0117 a0001c0001t0009g0011 a0001c0001t0009g0078 others(4): Show |
8 | HG00733.hp2 HG01255.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.894+1572dupT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066860 | |||||||
| chr22:50066892 | G | C | 7 | a0001c0001t0002g0117 a0001c0001t0009g0011 a0001c0001t0009g0078 others(4): Show |
8 | HG00733.hp2 HG01255.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.894+1541C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066892 | |||||||
| chr22:50066906 | GC | G | 48 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(45): Show |
52 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.894+1526delG | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066906 | |||||||
| chr22:50067078 | G | A | 2 | a0001c0001t0001g0062 a0001c0009t0014g0105 |
2 | HG00733.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.894+1355C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067078 | |||||||
| chr22:50067155 | A | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+1278T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067155 | |||||||
| chr22:50067258 | G | A | 1 | a0001c0001t0009g0088 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.894+1175C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067258 | |||||||
| chr22:50067390 | A | G | 21 | a0001c0001t0003g0004 a0001c0001t0003g0169 a0001c0001t0003g0170 others(18): Show |
23 | HG00099.hp1 HG00741.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.894+1043T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067390 | |||||||
| chr22:50067430 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+1003A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067430 | |||||||
| chr22:50067446 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.894+987G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067446 | |||||||
| chr22:50067454 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+979C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067454 | |||||||
| chr22:50067478 | A | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+955T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067478 | |||||||
| chr22:50067493 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+940A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067493 | |||||||
| chr22:50067495 | T | TC | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+937dupG | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067495 | |||||||
| chr22:50067495 | TCCCCTGT others(17): Show |
T | 3 | a0001c0001t0002g0117 a0001c0001t0012g0108 a0001c0001t0012g0116 |
3 | HG00733.hp2 HG02148.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.894+914_894+937del others(24): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067495 | |||||||
| chr22:50067497 | C | G | 1 | a0001c0001t0003g0170 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.894+936G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067497 | |||||||
| chr22:50067500 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+933A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067500 | |||||||
| chr22:50067524 | T | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0031 others(15): Show |
21 | HG00673.hp1 HG00741.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.894+909A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067524 | |||||||
| chr22:50067525 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+908C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067525 | |||||||
| chr22:50067545 | C | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+888G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067545 | |||||||
| chr22:50067549 | A | G | 7 | a0001c0001t0023g0145 a0001c0005t0013g0064 a0002c0002t0008g0165 others(4): Show |
7 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.894+884T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067549 | |||||||
| chr22:50067573 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.894+860C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067573 | |||||||
| chr22:50067596 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+837C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067596 | |||||||
| chr22:50067601 | GCAGTGAC others(12): Show |
G | 56 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
63 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.894+813_894+831del others(19): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067601 | |||||||
| chr22:50067619 | A | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+814T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067619 | |||||||
| chr22:50067620 | T | TCAGG | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+812_894+813ins others(4): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067620 | |||||||
| chr22:50067639 | TCAGA | T | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+790_894+793del others(4): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067639 | |||||||
| chr22:50067672 | A | T | 1 | a0001c0001t0002g0159 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.894+761T>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067672 | |||||||
| chr22:50067689 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+744C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067689 | |||||||
| chr22:50067697 | C | T | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+736G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067697 | |||||||
| chr22:50067703 | CTCCATCA others(17): Show |
C | 1 | a0001c0001t0002g0146 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.894+706_894+729del others(24): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067703 | |||||||
| chr22:50067704 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+729A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067704 | |||||||
| chr22:50067712 | A | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+721T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067712 | |||||||
| chr22:50067720 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+713A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067720 | |||||||
| chr22:50067726 | CA | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+706delT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067726 | |||||||
| chr22:50067750 | CA | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+682delT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067750 | |||||||
| chr22:50067752 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+681A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067752 | |||||||
| chr22:50067772 | TC | T | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+660delG | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067772 | |||||||
| chr22:50067806 | A | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+627T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067806 | |||||||
| chr22:50067818 | T | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0065 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.894+615A>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067818 | |||||||
| chr22:50067819 | C | G | 1 | a0001c0001t0002g0155 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.894+614G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067819 | |||||||
| chr22:50067956 | A | C | 58 | a0001c0001t0001g0075 a0001c0001t0001g0103 a0001c0001t0001g0130 others(55): Show |
64 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.894+477T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067956 | |||||||
| chr22:50067963 | C | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0120 |
2 | NA18944.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.894+470G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067963 | |||||||
| chr22:50067971 | C | A | 6 | a0001c0001t0001g0096 a0002c0002t0008g0165 a0002c0002t0008g0166 others(3): Show |
6 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.894+462G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067971 | |||||||
| chr22:50068011 | C | T | 21 | a0001c0001t0003g0004 a0001c0001t0003g0169 a0001c0001t0003g0170 others(18): Show |
23 | HG00099.hp1 HG00741.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.894+422G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50068011 | |||||||
| chr22:50068234 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+199C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50068234 | |||||||
| chr22:50068239 | C | T | 57 | a0001c0001t0001g0075 a0001c0001t0001g0103 a0001c0001t0001g0130 others(54): Show |
63 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.894+194G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50068239 | |||||||
| chr22:50068305 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.894+128C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50068305 | |||||||
| chr22:50068381 | A | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+52T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50068381 | |||||||
| chr22:50068589 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0031 others(10): Show |
16 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.772-34G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068589 | |||||||
| chr22:50068590 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-35C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068590 | |||||||
| chr22:50068635 | G | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-80C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068635 | |||||||
| chr22:50068665 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-110A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068665 | |||||||
| chr22:50068725 | C | CT | 29 | a0001c0001t0001g0032 a0001c0001t0001g0086 a0001c0001t0001g0099 others(26): Show |
32 | HG00099.hp1 HG01070.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.772-171dupA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068725 | |||||||
| chr22:50068725 | C | CTT | 13 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0067 others(10): Show |
16 | HG00741.hp1 HG00741.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.772-172_772-171dup others(2): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068725 | |||||||
| chr22:50068725 | CT | C | 8 | a0001c0001t0001g0026 a0001c0001t0001g0065 a0001c0001t0002g0117 others(5): Show |
9 | HG01255.hp2 HG02148.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.772-171delA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068725 | |||||||
| chr22:50068725 | CTTTT | C | 46 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(43): Show |
50 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.772-174_772-171del others(4): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068725 | |||||||
| chr22:50068727 | T | TTTC | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-173_772-172ins others(3): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068727 | |||||||
| chr22:50068730 | T | C | 4 | a0001c0001t0001g0026 a0001c0001t0001g0065 a0001c0001t0024g0190 others(1): Show |
4 | HG02257.hp1 HG02280.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.772-175A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068730 | |||||||
| chr22:50068732 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-177A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068732 | |||||||
| chr22:50068872 | G | A | 1 | a0001c0009t0014g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.772-317C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068872 | |||||||
| chr22:50068918 | T | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-363A>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068918 | |||||||
| chr22:50068929 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-374C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068929 | |||||||
| chr22:50068978 | C | T | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-423G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068978 | |||||||
| chr22:50069098 | A | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-543T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069098 | |||||||
| chr22:50069310 | G | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-755C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069310 | |||||||
| chr22:50069357 | C | T | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-802G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069357 | |||||||
| chr22:50069372 | A | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-817T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069372 | |||||||
| chr22:50069410 | C | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0032 |
3 | HG02451.hp2 HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.772-855G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069410 | |||||||
| chr22:50069487 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-932C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069487 | |||||||
| chr22:50069512 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.772-957C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069512 | |||||||
| chr22:50069514 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.772-959G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069514 | |||||||
| chr22:50069515 | G | C | 1 | a0001c0001t0001g0044 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.772-960C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069515 | |||||||
| chr22:50069607 | C | T | 1 | a0001c0009t0014g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.771+920G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069607 | |||||||
| chr22:50069710 | C | T | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+817G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069710 | |||||||
| chr22:50069763 | C | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+764G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069763 | |||||||
| chr22:50069776 | G | A | 4 | a0001c0001t0001g0075 a0001c0001t0011g0030 a0001c0001t0011g0081 others(1): Show |
4 | HG02486.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.771+751C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069776 | |||||||
| chr22:50069902 | T | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+625A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069902 | |||||||
| chr22:50069920 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+607C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069920 | |||||||
| chr22:50069999 | C | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+528G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069999 | |||||||
| chr22:50070074 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0031 others(10): Show |
16 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.771+453G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070074 | |||||||
| chr22:50070139 | T | A | 1 | a0001c0009t0014g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.771+388A>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070139 | |||||||
| chr22:50070157 | G | A | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+370C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070157 | |||||||
| chr22:50070243 | A | T | 48 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(45): Show |
52 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.771+284T>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070243 | |||||||
| chr22:50070270 | C | T | 1 | a0001c0001t0003g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.771+257G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070270 | |||||||
| chr22:50070273 | A | C | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+254T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070273 | |||||||
| chr22:50070291 | C | T | 8 | a0001c0001t0002g0017 a0001c0001t0002g0102 a0001c0001t0002g0133 others(5): Show |
9 | NA18945.hp1 NA18947.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.771+236G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070291 | |||||||
| chr22:50070292 | G | A | 48 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(45): Show |
52 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.771+235C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070292 | |||||||
| chr22:50070321 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0031 others(10): Show |
16 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.771+206C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070321 | |||||||
| chr22:50070352 | A | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+175T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070352 | |||||||
| chr22:50070367 | A | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+160T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070367 | |||||||
| chr22:50070405 | G | T | 1 | a0001c0001t0003g0172 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.771+122C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070405 | |||||||
| chr22:50070409 | C | T | 2 | a0001c0001t0010g0014 a0001c0001t0016g0107 |
3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.771+118G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070409 | |||||||
| chr22:50070466 | A | G | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+61T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070466 | |||||||
| chr22:50070468 | G | T | 5 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+59C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070468 | |||||||
| chr22:50070755 | C | T | 1 | a0001c0001t0013g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.715-172G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50070755 | |||||||
| chr22:50070767 | G | A | 50 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
54 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.715-184C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50070767 | |||||||
| chr22:50071014 | G | A | 1 | a0004c0004t0021g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.715-431C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071014 | |||||||
| chr22:50071115 | C | CT | 18 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0048 others(15): Show |
22 | HG00673.hp1 HG01243.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.715-533dupA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071115 | |||||||
| chr22:50071246 | T | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
188 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.715-663A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071246 | |||||||
| chr22:50071323 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0031 others(10): Show |
16 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.715-740G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071323 | |||||||
| chr22:50071334 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.715-751G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071334 | |||||||
| chr22:50071461 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.715-878C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071461 | |||||||
| chr22:50071488 | C | T | 13 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0114 others(10): Show |
14 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.715-905G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071488 | |||||||
| chr22:50071489 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0065 a0001c0001t0024g0190 |
3 | HG02257.hp1 HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.715-906C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071489 | |||||||
| chr22:50071548 | A | G | 14 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0114 others(11): Show |
15 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.715-965T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071548 | |||||||
| chr22:50071582 | T | A | 1 | a0001c0001t0002g0139 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.715-999A>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071582 | |||||||
| chr22:50071586 | C | T | 13 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0114 others(10): Show |
14 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.715-1003G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071586 | |||||||
| chr22:50071590 | T | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(180): Show |
205 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.715-1007A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071590 | |||||||
| chr22:50071703 | T | A | 1 | a0001c0001t0002g0139 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.715-1120A>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071703 | |||||||
| chr22:50071829 | T | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(120): Show |
138 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.715-1246A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071829 | |||||||
| chr22:50071949 | G | A | 1 | a0001c0001t0002g0124 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.715-1366C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071949 | |||||||
| chr22:50071949 | G | C | 2 | a0001c0001t0010g0014 a0001c0001t0016g0107 |
3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.715-1366C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071949 | |||||||
| chr22:50071981 | G | C | 1 | a0001c0001t0002g0139 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.715-1398C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071981 | |||||||
| chr22:50071982 | C | T | 1 | a0001c0001t0002g0139 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.715-1399G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071982 | |||||||
| chr22:50072003 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.715-1420C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072003 | |||||||
| chr22:50072104 | A | T | 13 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0114 others(10): Show |
14 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.715-1521T>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072104 | |||||||
| chr22:50072161 | C | T | 1 | a0003c0003t0001g0068 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.715-1578G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072161 | |||||||
| chr22:50072180 | G | A | 1 | a0004c0004t0021g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.715-1597C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072180 | |||||||
| chr22:50072267 | A | G | 3 | a0001c0001t0001g0038 a0001c0001t0001g0047 a0001c0001t0001g0048 |
3 | HG02027.hp1 NA19060.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.715-1684T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072267 | |||||||
| chr22:50072420 | T | C | 14 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0114 others(11): Show |
15 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.714+1796A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072420 | |||||||
| chr22:50072496 | G | A | 12 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0114 others(9): Show |
13 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.714+1720C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072496 | |||||||
| chr22:50072534 | C | G | 2 | a0001c0001t0001g0083 a0001c0001t0013g0089 |
2 | HG01243.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.714+1682G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072534 | |||||||
| chr22:50072534 | C | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0031 others(11): Show |
17 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.714+1682G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072534 | |||||||
| chr22:50072601 | T | G | 1 | a0001c0001t0002g0139 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.714+1615A>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072601 | |||||||
| chr22:50072799 | T | C | 2 | a0001c0001t0004g0176 a0001c0001t0004g0181 |
2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.714+1417A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072799 | |||||||
| chr22:50072835 | T | C | 1 | a0001c0001t0002g0139 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.714+1381A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072835 | |||||||
| chr22:50072837 | C | G | 1 | a0001c0001t0002g0139 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.714+1379G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072837 | |||||||
| chr22:50072842 | G | T | 1 | a0001c0001t0002g0139 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.714+1374C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072842 | |||||||
| chr22:50072945 | T | C | 13 | a0001c0001t0001g0120 a0001c0001t0002g0114 a0001c0001t0002g0117 others(10): Show |
14 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.714+1271A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072945 | |||||||
| chr22:50072973 | A | C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0026 others(66): Show |
80 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.714+1243T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072973 | |||||||
| chr22:50072997 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | NA19066.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.714+1219C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072997 | |||||||
| chr22:50073026 | GGCAGTCC others(42): Show |
G | 1 | a0001c0001t0002g0123 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.714+1141_714+1189d others(51): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073026 | |||||||
| chr22:50073038 | G | A | 1 | a0001c0001t0003g0175 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.714+1178C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073038 | |||||||
| chr22:50073046 | C | CGCTCCCG others(42): Show |
14 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0114 others(11): Show |
15 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.714+1169_714+1170i others(51): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073046 | |||||||
| chr22:50073085 | C | G | 2 | a0001c0001t0010g0014 a0001c0001t0016g0107 |
3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.714+1131G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073085 | |||||||
| chr22:50073086 | C | T | 1 | a0001c0001t0003g0169 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.714+1130G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073086 | |||||||
| chr22:50073109 | C | T | 6 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(3): Show |
6 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+1107G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073109 | |||||||
| chr22:50073275 | A | G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0031 others(11): Show |
17 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.714+941T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073275 | |||||||
| chr22:50073317 | C | T | 6 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(3): Show |
6 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+899G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073317 | |||||||
| chr22:50073378 | C | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(15): Show |
21 | HG00544.hp2 HG02027.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.714+838G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073378 | |||||||
| chr22:50073390 | G | A | 1 | a0004c0004t0004g0164 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.714+826C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073390 | |||||||
| chr22:50073559 | G | C | 70 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0026 others(67): Show |
81 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.714+657C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073559 | |||||||
| chr22:50073683 | G | A | 2 | a0001c0001t0010g0014 a0001c0001t0016g0107 |
3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.714+533C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073683 | |||||||
| chr22:50073687 | T | G | 14 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0114 others(11): Show |
15 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.714+529A>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073687 | |||||||
| chr22:50073906 | A | G | 1 | a0001c0005t0013g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.714+310T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073906 | |||||||
| chr22:50074065 | C | G | 1 | a0001c0001t0002g0141 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.714+151G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50074065 | |||||||
| chr22:50074085 | T | G | 76 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0026 others(73): Show |
87 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.714+131A>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50074085 | |||||||
| chr22:50074086 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.714+130C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50074086 | |||||||
| chr22:50074188 | C | T | 36 | a0001c0001t0001g0120 a0001c0001t0001g0161 a0001c0001t0001g0185 others(33): Show |
39 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.714+28G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50074188 | |||||||
| chr22:50074341 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.598-9C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50074341 | |||||||
| chr22:50074504 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.598-172G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50074504 | |||||||
| chr22:50074796 | TG | T | 44 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0002g0001 others(41): Show |
49 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.598-465delC | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50074796 | |||||||
| chr22:50074976 | A | C | 28 | a0001c0001t0001g0026 a0001c0001t0001g0065 a0001c0001t0001g0120 others(25): Show |
32 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.598-644T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50074976 | |||||||
| chr22:50075020 | G | A | 1 | a0001c0001t0022g0098 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.598-688C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075020 | |||||||
| chr22:50075101 | AGGGCCGC others(25): Show |
A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0031 others(14): Show |
20 | HG00741.hp2 HG01071.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.598-801_598-770del others(32): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075101 | |||||||
| chr22:50075101 | AGGGCCGC others(57): Show |
A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0007t0001g0054 |
3 | NA18966.hp2 NA19060.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.598-833_598-770del others(64): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075101 | |||||||
| chr22:50075170 | C | CGCAACCA others(89): Show |
1 | a0001c0001t0001g0131 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.598-839_598-838ins others(96): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075170 | |||||||
| chr22:50075202 | C | A | 25 | a0001c0001t0001g0161 a0001c0001t0001g0185 a0001c0001t0001g0188 others(22): Show |
28 | HG00741.hp1 HG01070.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.598-870G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075202 | |||||||
| chr22:50075272 | G | C | 1 | a0001c0001t0001g0097 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.598-940C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075272 | |||||||
| chr22:50075285 | T | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0026 others(76): Show |
90 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.598-953A>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075285 | |||||||
| chr22:50075355 | G | A | 14 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0114 others(11): Show |
15 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.598-1023C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075355 | |||||||
| chr22:50075442 | C | T | 43 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(40): Show |
49 | HG00544.hp2 HG00741.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.598-1110G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075442 | |||||||
| chr22:50075691 | C | CAG | 186 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
208 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.597+1148_597+1149d others(4): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075691 | |||||||
| chr22:50075718 | G | GA | 6 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(3): Show |
6 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.597+1122dupT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075718 | |||||||
| chr22:50075969 | C | G | 18 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(15): Show |
21 | HG00544.hp2 HG02027.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.597+872G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075969 | |||||||
| chr22:50076032 | T | C | 15 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0113 others(12): Show |
16 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.597+809A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076032 | |||||||
| chr22:50076076 | C | T | 1 | a0001c0001t0003g0177 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.597+765G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076076 | |||||||
| chr22:50076182 | C | CAT | 15 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0113 others(12): Show |
16 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.597+658_597+659ins others(2): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076182 | |||||||
| chr22:50076226 | A | G | 3 | a0001c0001t0009g0011 a0001c0001t0009g0078 a0001c0001t0009g0088 |
4 | HG01255.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+615T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076226 | |||||||
| chr22:50076283 | G | A | 6 | a0002c0002t0008g0165 a0002c0002t0008g0166 a0002c0002t0008g0167 others(3): Show |
6 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.597+558C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076283 | |||||||
| chr22:50076393 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.597+448T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076393 | |||||||
| chr22:50076415 | C | T | 1 | a0001c0007t0001g0054 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.597+426G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076415 | |||||||
| chr22:50076470 | A | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0026 others(68): Show |
79 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.597+371T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076470 | |||||||
| chr22:50076554 | C | CA | 6 | a0001c0001t0001g0022 a0001c0001t0001g0034 a0001c0001t0001g0048 others(3): Show |
6 | HG00099.hp1 HG02293.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.597+286dupT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076554 | |||||||
| chr22:50076554 | CA | C | 6 | a0001c0001t0001g0042 a0001c0001t0002g0114 a0001c0001t0003g0182 others(3): Show |
7 | HG00673.hp2 HG01192.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.597+286delT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076554 | |||||||
| chr22:50076577 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0065 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.597+264C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076577 | |||||||
| chr22:50076807 | T | C | 14 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0031 others(11): Show |
17 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.597+34A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076807 | |||||||
| chr22:50077030 | G | A | 169 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
189 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.526-118C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 6/11 | chr22 | 50077030 | |||||||
| chr22:50077208 | G | A | 1 | a0001c0001t0024g0190 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.525+193C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 6/11 | chr22 | 50077208 | |||||||
| chr22:50077248 | C | T | 21 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0003g0004 others(18): Show |
23 | HG00741.hp1 HG01070.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.525+153G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 6/11 | chr22 | 50077248 | |||||||
| chr22:50077337 | C | T | 15 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0113 others(12): Show |
16 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.525+64G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 6/11 | chr22 | 50077337 | |||||||
| chr22:50077379 | C | T | 15 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0113 others(12): Show |
16 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.525+22G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 6/11 | chr22 | 50077379 | |||||||
| chr22:50077512 | G | T | 1 | a0001c0001t0001g0022 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.424-10C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077512 | |||||||
| chr22:50077611 | C | T | 3 | a0001c0001t0001g0075 a0001c0001t0011g0081 a0001c0001t0017g0082 |
3 | HG02486.hp2 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.424-109G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077611 | |||||||
| chr22:50077766 | T | C | 43 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0002g0001 others(40): Show |
48 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.424-264A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077766 | |||||||
| chr22:50077792 | G | A | 1 | a0005c0008t0008g0119 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.424-290C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077792 | |||||||
| chr22:50077865 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.424-363T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077865 | |||||||
| chr22:50077939 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0032 others(1): Show |
5 | HG02258.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.424-437C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077939 | |||||||
| chr22:50077991 | A | AT | 33 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0080 others(30): Show |
37 | HG00741.hp1 HG01106.hp2 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.424-490dupA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077991 | |||||||
| chr22:50077991 | A | ATT | 6 | a0001c0005t0013g0064 a0002c0002t0008g0165 a0002c0002t0008g0166 others(3): Show |
6 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.424-491_424-490dup others(2): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077991 | |||||||
| chr22:50077991 | A | ATTT | 14 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0114 others(11): Show |
15 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.424-492_424-490dup others(3): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077991 | |||||||
| chr22:50077991 | AT | A | 8 | a0001c0001t0001g0050 a0001c0001t0001g0058 a0001c0001t0001g0059 others(5): Show |
8 | HG02055.hp2 HG02056.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.424-490delA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077991 | |||||||
| chr22:50078178 | G | C | 1 | a0001c0001t0012g0108 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.424-676C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50078178 | |||||||
| chr22:50078226 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0065 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.424-724C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50078226 | |||||||
| chr22:50078608 | G | A | 2 | a0001c0001t0002g0156 a0001c0001t0024g0190 |
2 | HG02257.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.424-1106C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50078608 | |||||||
| chr22:50078631 | C | G | 1 | a0001c0001t0002g0140 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.424-1129G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50078631 | |||||||
| chr22:50078736 | CA | C | 5 | a0001c0001t0002g0127 a0001c0001t0002g0139 a0001c0001t0020g0189 others(2): Show |
5 | HG00438.hp1 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+1181delT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50078736 | |||||||
| chr22:50078900 | G | A | 15 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0113 others(12): Show |
16 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.423+1018C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50078900 | |||||||
| chr22:50079009 | C | T | 3 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0001g0074 |
3 | HG02055.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.423+909G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079009 | |||||||
| chr22:50079252 | C | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0065 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.423+666G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079252 | |||||||
| chr22:50079313 | A | G | 15 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0113 others(12): Show |
16 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.423+605T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079313 | |||||||
| chr22:50079348 | C | T | 21 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0003g0004 others(18): Show |
23 | HG00741.hp1 HG01070.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.423+570G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079348 | |||||||
| chr22:50079500 | C | CT | 20 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0026 others(17): Show |
23 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.423+417dupA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079500 | |||||||
| chr22:50079500 | C | CTTT | 9 | a0001c0001t0001g0120 a0001c0001t0002g0114 a0001c0001t0002g0117 others(6): Show |
10 | HG00673.hp2 HG01358.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.423+415_423+417dup others(3): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079500 | |||||||
| chr22:50079500 | C | CTTTT | 6 | a0001c0001t0002g0106 a0001c0001t0002g0113 a0001c0001t0006g0112 others(3): Show |
6 | HG00621.hp1 HG00733.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.423+414_423+417dup others(4): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079500 | |||||||
| chr22:50079500 | CT | C | 24 | a0001c0001t0001g0045 a0001c0001t0001g0185 a0001c0001t0001g0188 others(21): Show |
26 | HG00741.hp1 HG01070.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.423+417delA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079500 | |||||||
| chr22:50079500 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0004g0056 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.423+406_423+417del others(12): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079500 | |||||||
| chr22:50079767 | T | C | 2 | a0001c0001t0020g0189 a0001c0001t0024g0190 |
2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.423+151A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079767 | |||||||
| chr22:50079797 | A | C | 2 | a0004c0004t0004g0164 a0004c0004t0021g0163 |
2 | HG03471.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.423+121T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079797 | |||||||
| chr22:50079810 | T | C | 17 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0113 others(14): Show |
18 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.423+108A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079810 | |||||||
| chr22:50079896 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.423+22G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079896 | |||||||
| chr22:50080222 | G | A | 2 | a0001c0001t0020g0189 a0001c0001t0024g0190 |
2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.321+122C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 4/11 | chr22 | 50080222 | |||||||
| chr22:50080266 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.321+78T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 4/11 | chr22 | 50080266 | |||||||
| chr22:50080294 | A | G | 184 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
206 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.321+50T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 4/11 | chr22 | 50080294 | |||||||
| chr22:50080749 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.268-352T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50080749 | |||||||
| chr22:50080903 | G | C | 2 | a0001c0001t0019g0021 a0004c0004t0004g0164 |
2 | HG00438.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.268-506C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50080903 | |||||||
| chr22:50080982 | G | A | 1 | a0001c0005t0013g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.268-585C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50080982 | |||||||
| chr22:50081007 | A | AAAAAAGA others(23): Show |
1 | a0001c0001t0002g0127 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.268-640_268-611dup others(30): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081007 | |||||||
| chr22:50081009 | A | AAAAAGAA others(10): Show |
1 | a0001c0001t0001g0067 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.268-613_268-612ins others(17): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAAAG | 7 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
8 | HG01243.hp2 HG01256.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.268-616_268-613dup others(4): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAAAGAAA others(1): Show |
8 | a0001c0001t0001g0013 a0001c0001t0001g0090 a0001c0001t0001g0093 others(5): Show |
9 | HG00544.hp1 HG01243.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.268-620_268-613dup others(8): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAAAGAAA others(5): Show |
10 | a0001c0001t0001g0012 a0001c0001t0001g0046 a0001c0001t0001g0047 others(7): Show |
11 | HG01358.hp1 HG01361.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.268-624_268-613dup others(12): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAAAGAAA others(9): Show |
15 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
18 | HG01256.hp1 HG01258.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.268-628_268-613dup others(16): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAAAGAAA others(13): Show |
19 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0031 others(16): Show |
22 | HG00733.hp1 HG00733.hp2 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.268-632_268-613dup others(20): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAAAGAAA others(30): Show |
1 | a0004c0004t0021g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.268-613_268-612ins others(37): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAAAGAAA others(17): Show |
22 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0023 others(19): Show |
24 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.268-636_268-613dup others(24): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAAAGAAA others(21): Show |
16 | a0001c0001t0001g0007 a0001c0001t0001g0051 a0001c0001t0001g0076 others(13): Show |
17 | HG00741.hp1 HG01070.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.268-640_268-613dup others(28): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAAAGAAA others(25): Show |
7 | a0001c0001t0001g0019 a0001c0001t0001g0037 a0001c0001t0001g0188 others(4): Show |
8 | HG01255.hp2 HG02451.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.268-644_268-613dup others(32): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAAAGAAA others(31): Show |
2 | a0001c0001t0002g0159 a0001c0001t0002g0160 |
2 | HG01255.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.268-613_268-612ins others(38): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAAAGAAA others(29): Show |
2 | a0001c0001t0001g0032 a0001c0001t0012g0108 |
2 | HG02148.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.268-648_268-613dup others(36): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAAAGAAA others(33): Show |
3 | a0001c0001t0001g0036 a0001c0001t0016g0107 a0001c0001t0020g0189 |
3 | NA18952.hp1 NA19043.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.268-652_268-613dup others(40): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAAGAAAG others(12): Show |
1 | a0001c0001t0001g0040 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.268-613_268-612ins others(19): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAAGAAAG others(16): Show |
2 | a0001c0001t0001g0022 a0001c0001t0001g0052 |
2 | HG03942.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.268-613_268-612ins others(23): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAAGAAAG others(24): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0125 a0001c0001t0007g0049 |
3 | HG03239.hp1 NA19062.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.268-613_268-612ins others(31): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAAGAAAG others(28): Show |
1 | a0003c0003t0001g0066 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.268-613_268-612ins others(35): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAAGAGAA others(18): Show |
1 | a0001c0001t0001g0034 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.268-613_268-612ins others(25): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAGAAAGA others(11): Show |
2 | a0001c0001t0001g0039 a0001c0001t0007g0029 |
2 | HG01175.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.268-613_268-612ins others(18): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAGAAAGA others(15): Show |
1 | a0001c0001t0006g0111 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.268-613_268-612ins others(22): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAGAAAGA others(19): Show |
1 | a0001c0001t0001g0050 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.268-613_268-612ins others(26): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AAGAAGAA others(10): Show |
1 | a0001c0001t0001g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.268-613_268-612ins others(17): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AGAAAGAA others(14): Show |
1 | a0001c0001t0019g0021 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.268-613_268-612ins others(21): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AGAAAGAA others(22): Show |
1 | a0001c0001t0001g0075 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.268-613_268-612ins others(29): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | A | AGAAAGAA others(34): Show |
1 | a0001c0001t0001g0035 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.268-613_268-612ins others(41): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081009 | AAAAG | A | 2 | a0001c0001t0005g0002 a0001c0001t0005g0028 |
4 | HG02055.hp1 HG02258.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-616_268-613del others(4): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | |||||||
| chr22:50081013 | G | GAAAGAAA others(19): Show |
6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0002g0016 others(3): Show |
7 | HG01106.hp1 HG02280.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.268-642_268-617dup others(26): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081013 | |||||||
| chr22:50081014 | A | AAAGAAAG others(20): Show |
1 | a0001c0001t0002g0124 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.268-644_268-618dup others(27): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081014 | |||||||
| chr22:50081017 | G | GAAAGAAA others(15): Show |
25 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0102 others(22): Show |
29 | HG00099.hp2 HG00621.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.268-642_268-621dup others(22): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081017 | |||||||
| chr22:50081017 | G | GAAAGAAA others(19): Show |
4 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(1): Show |
4 | HG02015.hp1 HG02148.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-646_268-621dup others(26): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081017 | |||||||
| chr22:50081021 | G | GAAAGAAA others(11): Show |
2 | a0001c0001t0002g0123 a0001c0001t0002g0162 |
2 | HG02135.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.268-642_268-625dup others(18): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081021 | |||||||
| chr22:50081025 | G | GAAAGAAA others(7): Show |
1 | a0006c0006t0002g0157 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.268-642_268-629dup others(14): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081025 | |||||||
| chr22:50081029 | G | GAAAGAAA others(16): Show |
1 | a0001c0001t0002g0158 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.268-633_268-632ins others(23): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081029 | |||||||
| chr22:50081033 | G | GAAAGAAA others(43): Show |
1 | a0001c0005t0013g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.268-637_268-636ins others(50): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081033 | |||||||
| chr22:50081037 | G | GAAAGAAA others(38): Show |
1 | a0001c0001t0004g0187 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.268-641_268-640ins others(45): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081037 | |||||||
| chr22:50081049 | G | GAAAGAAA others(7): Show |
1 | a0001c0001t0001g0074 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.268-653_268-652ins others(14): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081049 | |||||||
| chr22:50081049 | G | GAAAGAAA others(11): Show |
2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.268-653_268-652ins others(18): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081049 | |||||||
| chr22:50081049 | G | GAAAGAAA others(15): Show |
1 | a0001c0001t0001g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.268-653_268-652ins others(22): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081049 | |||||||
| chr22:50081049 | G | GAAAGAAA others(19): Show |
1 | a0001c0001t0001g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.268-653_268-652ins others(26): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081049 | |||||||
| chr22:50081049 | G | GAAAGAAA others(23): Show |
1 | a0001c0001t0001g0003 | 3 | HG00741.hp2 HG01891.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.268-653_268-652ins others(30): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081049 | |||||||
| chr22:50081049 | G | GAAAGAAA others(27): Show |
2 | a0001c0001t0001g0069 a0003c0003t0001g0068 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.268-653_268-652ins others(34): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081049 | |||||||
| chr22:50081151 | C | T | 17 | a0001c0001t0001g0120 a0001c0001t0002g0106 a0001c0001t0002g0113 others(14): Show |
18 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.268-754G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081151 | |||||||
| chr22:50081203 | C | T | 1 | a0001c0009t0014g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.268-806G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081203 | |||||||
| chr22:50081215 | T | C | 63 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0031 others(60): Show |
74 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.268-818A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081215 | |||||||
| chr22:50081338 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.268-941C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081338 | |||||||
| chr22:50081439 | ACAGCCTT others(8): Show |
A | 2 | a0001c0001t0002g0159 a0001c0001t0002g0160 |
2 | HG01255.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.268-1057_268-1043d others(17): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081439 | |||||||
| chr22:50081444 | C | T | 3 | a0001c0001t0002g0136 a0001c0001t0002g0139 a0001c0001t0002g0152 |
3 | HG02015.hp1 HG02074.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.268-1047G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081444 | |||||||
| chr22:50081549 | G | A | 3 | a0001c0001t0002g0106 a0001c0001t0010g0014 a0001c0001t0016g0107 |
4 | HG02004.hp2 HG02273.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-1152C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081549 | |||||||
| chr22:50081553 | C | A | 2 | a0001c0001t0002g0159 a0001c0001t0002g0160 |
2 | HG01255.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.268-1156G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081553 | |||||||
| chr22:50081610 | C | T | 3 | a0001c0001t0002g0106 a0001c0001t0010g0014 a0001c0001t0016g0107 |
4 | HG02004.hp2 HG02273.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-1213G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081610 | |||||||
| chr22:50081623 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.268-1226C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081623 | |||||||
| chr22:50081703 | G | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0067 a0001c0001t0001g0069 others(7): Show |
12 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.268-1306C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081703 | |||||||
| chr22:50081762 | G | A | 17 | a0001c0001t0001g0025 a0001c0001t0001g0120 a0001c0001t0002g0113 others(14): Show |
18 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.267+1322C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081762 | |||||||
| chr22:50081955 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.267+1129C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081955 | |||||||
| chr22:50082044 | C | T | 16 | a0001c0001t0001g0120 a0001c0001t0002g0113 a0001c0001t0002g0114 others(13): Show |
17 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.267+1040G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082044 | |||||||
| chr22:50082050 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.267+1034G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082050 | |||||||
| chr22:50082124 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.267+960G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082124 | |||||||
| chr22:50082139 | G | C | 2 | a0001c0001t0001g0161 a0001c0001t0024g0190 |
2 | HG02257.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.267+945C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082139 | |||||||
| chr22:50082157 | C | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(5): Show |
8 | HG00438.hp2 HG02015.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.267+927G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082157 | |||||||
| chr22:50082163 | G | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(15): Show |
21 | HG00544.hp2 HG02027.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.267+921C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082163 | |||||||
| chr22:50082167 | GTGGGGTC others(24): Show |
G | 3 | a0001c0001t0001g0104 a0001c0009t0014g0105 a0004c0004t0021g0163 |
3 | HG01496.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.267+886_267+916del others(31): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082167 | |||||||
| chr22:50082174 | CCGCGGCT others(55): Show |
C | 15 | a0001c0001t0001g0120 a0001c0001t0002g0113 a0001c0001t0002g0114 others(12): Show |
16 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.267+848_267+909del others(62): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082174 | |||||||
| chr22:50082205 | C | G | 1 | a0001c0001t0011g0030 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.267+879G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082205 | |||||||
| chr22:50082247 | G | A | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.267+837C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082247 | |||||||
| chr22:50082290 | A | C | 1 | a0004c0004t0021g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.267+794T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082290 | |||||||
| chr22:50082409 | C | T | 88 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0031 others(85): Show |
101 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.267+675G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082409 | |||||||
| chr22:50082450 | A | G | 16 | a0001c0001t0001g0120 a0001c0001t0002g0113 a0001c0001t0002g0114 others(13): Show |
17 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.267+634T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082450 | |||||||
| chr22:50082467 | G | A | 1 | a0004c0004t0004g0164 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.267+617C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082467 | |||||||
| chr22:50082701 | A | G | 16 | a0001c0001t0001g0120 a0001c0001t0002g0113 a0001c0001t0002g0114 others(13): Show |
17 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.267+383T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082701 | |||||||
| chr22:50082728 | A | G | 16 | a0001c0001t0001g0120 a0001c0001t0002g0113 a0001c0001t0002g0114 others(13): Show |
17 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.267+356T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082728 | |||||||
| chr22:50082910 | C | A | 1 | a0001c0001t0005g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.267+174G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082910 | |||||||
| chr22:50083305 | A | G | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.178-132T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50083305 | |||||||
| chr22:50083346 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.178-173G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50083346 | |||||||
| chr22:50083346 | C | T | 16 | a0001c0001t0001g0120 a0001c0001t0002g0113 a0001c0001t0002g0114 others(13): Show |
17 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.178-173G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50083346 | |||||||
| chr22:50083352 | C | A | 16 | a0001c0001t0001g0120 a0001c0001t0002g0113 a0001c0001t0002g0114 others(13): Show |
17 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.178-179G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50083352 | |||||||
| chr22:50083707 | T | C | 16 | a0001c0001t0001g0120 a0001c0001t0002g0113 a0001c0001t0002g0114 others(13): Show |
17 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.178-534A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50083707 | |||||||
| chr22:50083724 | G | A | 44 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0130 others(41): Show |
49 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.178-551C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50083724 | |||||||
| chr22:50083886 | T | C | 102 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0031 others(99): Show |
115 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.178-713A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50083886 | |||||||
| chr22:50084032 | G | A | 4 | a0001c0001t0001g0161 a0001c0001t0002g0162 a0001c0001t0020g0189 others(1): Show |
4 | HG02135.hp2 HG02257.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+694C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50084032 | |||||||
| chr22:50084037 | C | T | 43 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(40): Show |
47 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.177+689G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50084037 | |||||||
| chr22:50084095 | C | T | 2 | a0004c0004t0004g0164 a0004c0004t0021g0163 |
2 | HG03471.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.177+631G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50084095 | |||||||
| chr22:50084248 | G | A | 2 | a0004c0004t0004g0164 a0004c0004t0021g0163 |
2 | HG03471.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.177+478C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50084248 | |||||||
| chr22:50084273 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0032 others(1): Show |
5 | HG02258.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+453G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50084273 | |||||||
| chr22:50084501 | A | G | 2 | a0004c0004t0004g0164 a0004c0004t0021g0163 |
2 | HG03471.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.177+225T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50084501 | |||||||
| chr22:50084649 | C | T | 1 | a0001c0001t0007g0029 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.177+77G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50084649 | |||||||
| chr22:50084978 | A | G | 5 | a0001c0001t0001g0026 a0001c0001t0005g0002 a0001c0001t0005g0005 others(2): Show |
8 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-59-17T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 1/11 | chr22 | 50084978 | |||||||
| chr22:50084988 | G | A | 2 | a0004c0004t0004g0164 a0004c0004t0021g0163 |
2 | HG03471.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-59-27C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 1/11 | chr22 | 50084988 | |||||||
| chr22:50085004 | T | C | 25 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0003g0004 others(22): Show |
27 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.-59-43A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 1/11 | chr22 | 50085004 | |||||||
| chr22:50085241 | G | A | 2 | a0001c0001t0020g0189 a0001c0001t0024g0190 |
2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-60+114C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 1/11 | chr22 | 50085241 | |||||||
| chr22:50085316 | A | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(5): Show |
8 | HG00438.hp2 HG02015.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.-60+39T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 1/11 | chr22 | 50085316 |