Search by Gene
| geneid | 255231 |
|---|---|
| ensemblid | ENSG00000153898.13 |
| hgncid | 13357 |
| symbol | MCOLN2 |
| name | mucolipin TRP cation channel 2 |
| refseq_nuc | NM_153259.4 |
| refseq_prot | NP_694991.2 |
| ensembl_nuc | ENST00000370608.8 |
| ensembl_prot | ENSP00000359640.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 84925583 |
| end | 84997113 |
| strand | - |
| ver | v1.2 |
| region | chr1:84925583-84997113 |
| region5000 | chr1:84920583-85002113 |
| regionname0 | MCOLN2_chr1_84925583_84997113 |
| regionname5000 | MCOLN2_chr1_84920583_85002113 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 566 | 316 | 56 | 63 | 150 | 12 | 33 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0002 | 0/0 | 566 | 10 | 8 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0003 | 0/0 | 566 | 9 | 9 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0004 | 0/0 | 566 | 4 | 4 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0005 | 0/0 | 566 | 3 | 3 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0006 | 0/0 | 566 | 3 | 1 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0007 | 0/0 | 566 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0008 | 0/0 | 566 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0009 | 0/0 | 566 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0010 | 0/0 | 566 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0011 | 0/0 | 566 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1701 | 315 | 56 | 63 | 149 | 12 | 33 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| c0002 | 0/0 | 1701 | 10 | 8 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| c0003 | 0/0 | 1701 | 9 | 9 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| c0004 | 0/0 | 1701 | 4 | 4 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| c0005 | 0/0 | 1701 | 3 | 3 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| c0006 | 0/0 | 1701 | 3 | 1 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| c0007 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| c0008 | 0/0 | 1701 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| c0009 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| c0010 | 0/0 | 1701 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| c0011 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| c0012 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1344 | 88 | 38 | 12 | 28 | 3 | 7 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0002 | 0/0 | 1344 | 73 | 12 | 17 | 31 | 4 | 9 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0003 | 0/0 | 1344 | 51 | 0 | 20 | 23 | 2 | 6 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0004 | 0/0 | 1344 | 25 | 4 | 6 | 14 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0005 | 0/0 | 1344 | 18 | 18 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0006 | 0/0 | 1345 | 16 | 0 | 0 | 16 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0007 | 0/0 | 1345 | 14 | 0 | 1 | 8 | 0 | 5 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0008 | 0/0 | 1343 | 10 | 0 | 1 | 8 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0009 | 0/0 | 1343 | 9 | 0 | 2 | 7 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0010 | 0/1 | 1346 | 5 | 0 | 0 | 4 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0011 | 0/0 | 1344 | 5 | 0 | 4 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0012 | 0/0 | 1343 | 4 | 0 | 0 | 1 | 0 | 3 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0013 | 0/0 | 1344 | 3 | 2 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0014 | 0/0 | 1345 | 3 | 3 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0015 | 0/0 | 1346 | 3 | 0 | 1 | 2 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0016 | 0/0 | 1345 | 2 | 0 | 0 | 1 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0017 | 0/0 | 1344 | 2 | 0 | 1 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0018 | 0/0 | 1344 | 2 | 1 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0019 | 0/0 | 1345 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0020 | 1/0 | 1344 | 1 | 0 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0021 | 0/0 | 1345 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0022 | 0/0 | 1344 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0023 | 0/0 | 1344 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0024 | 0/0 | 1343 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0025 | 0/0 | 1344 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0026 | 0/0 | 1345 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0027 | 0/0 | 1345 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0028 | 0/0 | 1345 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0029 | 0/0 | 1344 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0030 | 0/0 | 1344 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0031 | 0/0 | 1345 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0032 | 0/0 | 1344 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0033 | 0/0 | 1345 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0034 | 0/0 | 1344 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| t0035 | 0/0 | 1344 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0023 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0209 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 315 | 56 | 63 | 149 | 12 | 33 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0011 | a0001 | c0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0002c0002 | a0002 | c0002 | 0/0 | 10 | 8 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0003c0003 | a0003 | c0003 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0004c0004 | a0004 | c0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0005c0005 | a0005 | c0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0006c0006 | a0006 | c0006 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0007c0007 | a0007 | c0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0008c0012 | a0008 | c0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0009c0008 | a0009 | c0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0010c0010 | a0010 | c0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0011c0009 | a0011 | c0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/0 | 72 | 22 | 12 | 28 | 3 | 7 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 67 | 10 | 14 | 31 | 4 | 8 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 50 | 0 | 19 | 23 | 2 | 6 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 23 | 3 | 6 | 13 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 11 | 11 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 14 | 0 | 1 | 8 | 0 | 5 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 10 | 0 | 1 | 8 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/1 | 5 | 0 | 0 | 4 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0015 | a0001 | c0001 | t0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0016 | a0001 | c0001 | t0016 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0017 | a0001 | c0001 | t0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0018 | a0001 | c0001 | t0018 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0020 | a0001 | c0001 | t0020 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0021 | a0001 | c0001 | t0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0022 | a0001 | c0001 | t0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0023 | a0001 | c0001 | t0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0024 | a0001 | c0001 | t0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0026 | a0001 | c0001 | t0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0027 | a0001 | c0001 | t0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0029 | a0001 | c0001 | t0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0030 | a0001 | c0001 | t0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0031 | a0001 | c0001 | t0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0032 | a0001 | c0001 | t0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0033 | a0001 | c0001 | t0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0034 | a0001 | c0001 | t0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0001t0035 | a0001 | c0001 | t0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0001c0011t0004 | a0001 | c0011 | t0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0002c0002t0001 | a0002 | c0002 | t0001 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0002c0002t0002 | a0002 | c0002 | t0002 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0002c0002t0028 | a0002 | c0002 | t0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0003c0003t0001 | a0003 | c0003 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0003c0003t0005 | a0003 | c0003 | t0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0003c0003t0013 | a0003 | c0003 | t0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0004c0004t0001 | a0004 | c0004 | t0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0005c0005t0001 | a0005 | c0005 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0006c0006t0001 | a0006 | c0006 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0006c0006t0003 | a0006 | c0006 | t0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0006c0006t0025 | a0006 | c0006 | t0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0007c0007t0004 | a0007 | c0007 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0008c0012t0005 | a0008 | c0012 | t0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0009c0008t0002 | a0009 | c0008 | t0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0010c0010t0002 | a0010 | c0010 | t0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| a0011c0009t0001 | a0011 | c0009 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0104 | a0001 | c0001 | t0001 | g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0013 | a0001 | c0001 | t0002 | g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0189 | a0001 | c0001 | t0002 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0191 | a0001 | c0001 | t0002 | g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0192 | a0001 | c0001 | t0002 | g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0193 | a0001 | c0001 | t0002 | g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0197 | a0001 | c0001 | t0002 | g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0198 | a0001 | c0001 | t0002 | g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0199 | a0001 | c0001 | t0002 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0200 | a0001 | c0001 | t0002 | g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0203 | a0001 | c0001 | t0002 | g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0205 | a0001 | c0001 | t0002 | g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0207 | a0001 | c0001 | t0002 | g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0212 | a0001 | c0001 | t0002 | g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0218 | a0001 | c0001 | t0002 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0219 | a0001 | c0001 | t0002 | g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0222 | a0001 | c0001 | t0002 | g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0224 | a0001 | c0001 | t0002 | g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0226 | a0001 | c0001 | t0002 | g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0228 | a0001 | c0001 | t0002 | g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0229 | a0001 | c0001 | t0002 | g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0230 | a0001 | c0001 | t0002 | g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0233 | a0001 | c0001 | t0002 | g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0235 | a0001 | c0001 | t0002 | g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0237 | a0001 | c0001 | t0002 | g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0242 | a0001 | c0001 | t0002 | g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0247 | a0001 | c0001 | t0002 | g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0248 | a0001 | c0001 | t0002 | g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0250 | a0001 | c0001 | t0002 | g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0253 | a0001 | c0001 | t0002 | g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0254 | a0001 | c0001 | t0002 | g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0255 | a0001 | c0001 | t0002 | g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0257 | a0001 | c0001 | t0002 | g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0260 | a0001 | c0001 | t0002 | g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0262 | a0001 | c0001 | t0002 | g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0264 | a0001 | c0001 | t0002 | g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0265 | a0001 | c0001 | t0002 | g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0269 | a0001 | c0001 | t0002 | g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0270 | a0001 | c0001 | t0002 | g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0276 | a0001 | c0001 | t0002 | g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0284 | a0001 | c0001 | t0002 | g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0285 | a0001 | c0001 | t0002 | g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0288 | a0001 | c0001 | t0002 | g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0289 | a0001 | c0001 | t0002 | g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0291 | a0001 | c0001 | t0002 | g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0293 | a0001 | c0001 | t0002 | g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0294 | a0001 | c0001 | t0002 | g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0296 | a0001 | c0001 | t0002 | g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0298 | a0001 | c0001 | t0002 | g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0300 | a0001 | c0001 | t0002 | g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0303 | a0001 | c0001 | t0002 | g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0304 | a0001 | c0001 | t0002 | g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0306 | a0001 | c0001 | t0002 | g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0308 | a0001 | c0001 | t0002 | g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0309 | a0001 | c0001 | t0002 | g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0313 | a0001 | c0001 | t0002 | g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0314 | a0001 | c0001 | t0002 | g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0317 | a0001 | c0001 | t0002 | g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0319 | a0001 | c0001 | t0002 | g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0320 | a0001 | c0001 | t0002 | g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0322 | a0001 | c0001 | t0002 | g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0323 | a0001 | c0001 | t0002 | g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0325 | a0001 | c0001 | t0002 | g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0326 | a0001 | c0001 | t0002 | g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0328 | a0001 | c0001 | t0002 | g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0329 | a0001 | c0001 | t0002 | g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0002g0330 | a0001 | c0001 | t0002 | g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0007 | a0001 | c0001 | t0003 | g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0008 | a0001 | c0001 | t0003 | g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0010 | a0001 | c0001 | t0003 | g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0011 | a0001 | c0001 | t0003 | g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0012 | a0001 | c0001 | t0003 | g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0014 | a0001 | c0001 | t0003 | g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0182 | a0001 | c0001 | t0003 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0183 | a0001 | c0001 | t0003 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0185 | a0001 | c0001 | t0003 | g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0186 | a0001 | c0001 | t0003 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0187 | a0001 | c0001 | t0003 | g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0188 | a0001 | c0001 | t0003 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0190 | a0001 | c0001 | t0003 | g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0194 | a0001 | c0001 | t0003 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0195 | a0001 | c0001 | t0003 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0201 | a0001 | c0001 | t0003 | g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0202 | a0001 | c0001 | t0003 | g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0206 | a0001 | c0001 | t0003 | g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0208 | a0001 | c0001 | t0003 | g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0210 | a0001 | c0001 | t0003 | g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0213 | a0001 | c0001 | t0003 | g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0214 | a0001 | c0001 | t0003 | g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0216 | a0001 | c0001 | t0003 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0238 | a0001 | c0001 | t0003 | g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0239 | a0001 | c0001 | t0003 | g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0240 | a0001 | c0001 | t0003 | g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0241 | a0001 | c0001 | t0003 | g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0249 | a0001 | c0001 | t0003 | g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0251 | a0001 | c0001 | t0003 | g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0252 | a0001 | c0001 | t0003 | g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0259 | a0001 | c0001 | t0003 | g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0266 | a0001 | c0001 | t0003 | g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0267 | a0001 | c0001 | t0003 | g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0280 | a0001 | c0001 | t0003 | g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0281 | a0001 | c0001 | t0003 | g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0290 | a0001 | c0001 | t0003 | g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0292 | a0001 | c0001 | t0003 | g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0297 | a0001 | c0001 | t0003 | g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0299 | a0001 | c0001 | t0003 | g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0301 | a0001 | c0001 | t0003 | g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0311 | a0001 | c0001 | t0003 | g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0316 | a0001 | c0001 | t0003 | g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0318 | a0001 | c0001 | t0003 | g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0003g0324 | a0001 | c0001 | t0003 | g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0047 | a0001 | c0001 | t0004 | g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0079 | a0001 | c0001 | t0004 | g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0081 | a0001 | c0001 | t0004 | g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0083 | a0001 | c0001 | t0004 | g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0091 | a0001 | c0001 | t0004 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0092 | a0001 | c0001 | t0004 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0094 | a0001 | c0001 | t0004 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0097 | a0001 | c0001 | t0004 | g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0102 | a0001 | c0001 | t0004 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0103 | a0001 | c0001 | t0004 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0127 | a0001 | c0001 | t0004 | g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0128 | a0001 | c0001 | t0004 | g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0129 | a0001 | c0001 | t0004 | g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0136 | a0001 | c0001 | t0004 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0137 | a0001 | c0001 | t0004 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0146 | a0001 | c0001 | t0004 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0148 | a0001 | c0001 | t0004 | g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0155 | a0001 | c0001 | t0004 | g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0156 | a0001 | c0001 | t0004 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0159 | a0001 | c0001 | t0004 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0171 | a0001 | c0001 | t0004 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0179 | a0001 | c0001 | t0004 | g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0004g0181 | a0001 | c0001 | t0004 | g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0005g0017 | a0001 | c0001 | t0005 | g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0005g0018 | a0001 | c0001 | t0005 | g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0005g0021 | a0001 | c0001 | t0005 | g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0005g0022 | a0001 | c0001 | t0005 | g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0005g0024 | a0001 | c0001 | t0005 | g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0005g0027 | a0001 | c0001 | t0005 | g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0005g0032 | a0001 | c0001 | t0005 | g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0005g0033 | a0001 | c0001 | t0005 | g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0005g0034 | a0001 | c0001 | t0005 | g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0005g0035 | a0001 | c0001 | t0005 | g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0005g0038 | a0001 | c0001 | t0005 | g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0006g0184 | a0001 | c0001 | t0006 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0006g0196 | a0001 | c0001 | t0006 | g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0006g0231 | a0001 | c0001 | t0006 | g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0006g0234 | a0001 | c0001 | t0006 | g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0006g0271 | a0001 | c0001 | t0006 | g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0006g0272 | a0001 | c0001 | t0006 | g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0006g0277 | a0001 | c0001 | t0006 | g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0006g0278 | a0001 | c0001 | t0006 | g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0006g0279 | a0001 | c0001 | t0006 | g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0006g0283 | a0001 | c0001 | t0006 | g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0006g0286 | a0001 | c0001 | t0006 | g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0006g0287 | a0001 | c0001 | t0006 | g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0006g0295 | a0001 | c0001 | t0006 | g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0006g0302 | a0001 | c0001 | t0006 | g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0006g0305 | a0001 | c0001 | t0006 | g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0006g0310 | a0001 | c0001 | t0006 | g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0007g0051 | a0001 | c0001 | t0007 | g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0007g0056 | a0001 | c0001 | t0007 | g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0007g0060 | a0001 | c0001 | t0007 | g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0007g0063 | a0001 | c0001 | t0007 | g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0007g0073 | a0001 | c0001 | t0007 | g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0007g0096 | a0001 | c0001 | t0007 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0007g0108 | a0001 | c0001 | t0007 | g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0007g0115 | a0001 | c0001 | t0007 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0007g0117 | a0001 | c0001 | t0007 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0007g0135 | a0001 | c0001 | t0007 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0007g0139 | a0001 | c0001 | t0007 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0007g0144 | a0001 | c0001 | t0007 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0007g0164 | a0001 | c0001 | t0007 | g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0007g0170 | a0001 | c0001 | t0007 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0008g0204 | a0001 | c0001 | t0008 | g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0008g0211 | a0001 | c0001 | t0008 | g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0008g0215 | a0001 | c0001 | t0008 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0008g0217 | a0001 | c0001 | t0008 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0008g0227 | a0001 | c0001 | t0008 | g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0008g0232 | a0001 | c0001 | t0008 | g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0008g0273 | a0001 | c0001 | t0008 | g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0008g0274 | a0001 | c0001 | t0008 | g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0008g0275 | a0001 | c0001 | t0008 | g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0008g0312 | a0001 | c0001 | t0008 | g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0009g0005 | a0001 | c0001 | t0009 | g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0009g0048 | a0001 | c0001 | t0009 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0009g0049 | a0001 | c0001 | t0009 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0009g0050 | a0001 | c0001 | t0009 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0009g0107 | a0001 | c0001 | t0009 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0009g0152 | a0001 | c0001 | t0009 | g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0009g0153 | a0001 | c0001 | t0009 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0009g0178 | a0001 | c0001 | t0009 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0010g0209 | a0001 | c0001 | t0010 | g0209 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0010g0225 | a0001 | c0001 | t0010 | g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0010g0258 | a0001 | c0001 | t0010 | g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0010g0261 | a0001 | c0001 | t0010 | g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0010g0263 | a0001 | c0001 | t0010 | g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0011g0331 | a0001 | c0001 | t0011 | g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0011g0332 | a0001 | c0001 | t0011 | g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0011g0333 | a0001 | c0001 | t0011 | g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0011g0334 | a0001 | c0001 | t0011 | g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0011g0335 | a0001 | c0001 | t0011 | g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0012g0220 | a0001 | c0001 | t0012 | g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0012g0256 | a0001 | c0001 | t0012 | g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0012g0268 | a0001 | c0001 | t0012 | g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0012g0307 | a0001 | c0001 | t0012 | g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0013g0026 | a0001 | c0001 | t0013 | g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0013g0037 | a0001 | c0001 | t0013 | g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0014g0015 | a0001 | c0001 | t0014 | g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0014g0019 | a0001 | c0001 | t0014 | g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0014g0020 | a0001 | c0001 | t0014 | g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0015g0125 | a0001 | c0001 | t0015 | g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0015g0168 | a0001 | c0001 | t0015 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0015g0176 | a0001 | c0001 | t0015 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0016g0126 | a0001 | c0001 | t0016 | g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0016g0172 | a0001 | c0001 | t0016 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0017g0100 | a0001 | c0001 | t0017 | g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0017g0158 | a0001 | c0001 | t0017 | g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0018g0223 | a0001 | c0001 | t0018 | g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0018g0244 | a0001 | c0001 | t0018 | g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0019g0036 | a0001 | c0001 | t0019 | g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0020g0023 | a0001 | c0001 | t0020 | g0023 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0021g0088 | a0001 | c0001 | t0021 | g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0022g0163 | a0001 | c0001 | t0022 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0023g0142 | a0001 | c0001 | t0023 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0024g0151 | a0001 | c0001 | t0024 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0026g0085 | a0001 | c0001 | t0026 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0027g0147 | a0001 | c0001 | t0027 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0029g0133 | a0001 | c0001 | t0029 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0030g0101 | a0001 | c0001 | t0030 | g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0031g0087 | a0001 | c0001 | t0031 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0032g0246 | a0001 | c0001 | t0032 | g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0033g0282 | a0001 | c0001 | t0033 | g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0034g0315 | a0001 | c0001 | t0034 | g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0001t0035g0321 | a0001 | c0001 | t0035 | g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0001c0011t0004g0112 | a0001 | c0011 | t0004 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0002c0002t0001g0052 | a0002 | c0002 | t0001 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0002c0002t0001g0058 | a0002 | c0002 | t0001 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0002c0002t0001g0061 | a0002 | c0002 | t0001 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0002c0002t0001g0065 | a0002 | c0002 | t0001 | g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0002c0002t0001g0122 | a0002 | c0002 | t0001 | g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0002c0002t0002g0009 | a0002 | c0002 | t0002 | g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0002c0002t0002g0236 | a0002 | c0002 | t0002 | g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0002c0002t0002g0243 | a0002 | c0002 | t0002 | g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0002c0002t0028g0105 | a0002 | c0002 | t0028 | g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0003c0003t0001g0086 | a0003 | c0003 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0003c0003t0001g0095 | a0003 | c0003 | t0001 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0003c0003t0005g0002 | a0003 | c0003 | t0005 | g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0003c0003t0005g0028 | a0003 | c0003 | t0005 | g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0003c0003t0005g0029 | a0003 | c0003 | t0005 | g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0003c0003t0005g0030 | a0003 | c0003 | t0005 | g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0003c0003t0005g0031 | a0003 | c0003 | t0005 | g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0003c0003t0013g0025 | a0003 | c0003 | t0013 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0004c0004t0001g0039 | a0004 | c0004 | t0001 | g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0004c0004t0001g0040 | a0004 | c0004 | t0001 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0004c0004t0001g0045 | a0004 | c0004 | t0001 | g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0004c0004t0001g0046 | a0004 | c0004 | t0001 | g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0005c0005t0001g0042 | a0005 | c0005 | t0001 | g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0005c0005t0001g0043 | a0005 | c0005 | t0001 | g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0005c0005t0001g0044 | a0005 | c0005 | t0001 | g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0006c0006t0001g0130 | a0006 | c0006 | t0001 | g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0006c0006t0003g0327 | a0006 | c0006 | t0003 | g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0006c0006t0025g0131 | a0006 | c0006 | t0025 | g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0007c0007t0004g0041 | a0007 | c0007 | t0004 | g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0008c0012t0005g0016 | a0008 | c0012 | t0005 | g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0009c0008t0002g0221 | a0009 | c0008 | t0002 | g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0010c0010t0002g0245 | a0010 | c0010 | t0002 | g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| a0011c0009t0001g0180 | a0011 | c0009 | t0001 | g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0240 | EUR | GBR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00140 | hp2 | a0001 | c0001 | t0016 | g0126 | EUR | GBR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00280 | hp1 | a0001 | c0001 | t0017 | g0100 | EUR | FIN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0276 | EUR | FIN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | FIN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0190 | EUR | FIN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00558 | hp1 | a0001 | c0001 | t0033 | g0282 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00597 | hp2 | a0001 | c0001 | t0007 | g0170 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0243 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00642 | hp2 | a0010 | c0010 | t0002 | g0245 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00673 | hp2 | a0001 | c0001 | t0015 | g0176 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG00741 | hp2 | a0006 | c0006 | t0003 | g0327 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0097 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0252 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0127 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01081 | hp2 | a0001 | c0001 | t0011 | g0335 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01099 | hp2 | a0006 | c0006 | t0025 | g0131 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01106 | hp1 | a0001 | c0001 | t0011 | g0334 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0063 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01109 | hp1 | a0001 | c0001 | t0011 | g0332 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0325 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0236 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01169 | hp1 | a0001 | c0001 | t0017 | g0158 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0181 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01257 | hp1 | a0001 | c0001 | t0030 | g0101 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0128 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0191 | EUR | IBS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0230 | EUR | IBS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01516 | hp1 | a0001 | c0001 | t0011 | g0331 | EUR | IBS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0200 | EUR | IBS | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01884 | hp2 | a0003 | c0003 | t0005 | g0002 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01928 | hp2 | a0001 | c0001 | t0008 | g0204 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01943 | hp1 | a0001 | c0001 | t0009 | g0005 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0324 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0148 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01978 | hp1 | a0001 | c0001 | t0009 | g0005 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0280 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01981 | hp2 | a0001 | c0001 | t0015 | g0125 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG01993 | hp2 | a0001 | c0001 | t0021 | g0088 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02056 | hp1 | a0001 | c0001 | t0008 | g0232 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0286 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02080 | hp1 | a0001 | c0001 | t0008 | g0211 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02080 | hp2 | a0001 | c0001 | t0008 | g0274 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02129 | hp1 | a0001 | c0011 | t0004 | g0112 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0231 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02132 | hp1 | a0001 | c0001 | t0006 | g0283 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02145 | hp1 | a0008 | c0012 | t0005 | g0016 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0320 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | CDX | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | CDX | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02165 | hp1 | a0001 | c0001 | t0008 | g0215 | EAS | CDX | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02257 | hp1 | a0004 | c0004 | t0001 | g0039 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02280 | hp2 | a0001 | c0001 | t0031 | g0087 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02300 | hp2 | a0001 | c0001 | t0011 | g0333 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02572 | hp1 | a0001 | c0001 | t0035 | g0321 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02572 | hp2 | a0007 | c0007 | t0004 | g0041 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02615 | hp2 | a0005 | c0005 | t0001 | g0044 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02622 | hp1 | a0001 | c0001 | t0014 | g0019 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02630 | hp1 | a0001 | c0001 | t0014 | g0020 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02647 | hp1 | a0003 | c0003 | t0001 | g0086 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02647 | hp2 | a0001 | c0001 | t0026 | g0085 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0201 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02683 | hp2 | a0001 | c0001 | t0007 | g0056 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02717 | hp1 | a0001 | c0001 | t0014 | g0015 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0065 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02818 | hp2 | a0003 | c0003 | t0005 | g0029 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0122 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0052 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02896 | hp2 | a0003 | c0003 | t0005 | g0031 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02897 | hp1 | a0003 | c0003 | t0005 | g0028 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02922 | hp1 | a0005 | c0005 | t0001 | g0042 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02965 | hp2 | a0004 | c0004 | t0001 | g0045 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0009 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02976 | hp2 | a0003 | c0003 | t0005 | g0030 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03017 | hp2 | a0001 | c0001 | t0018 | g0223 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0247 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03098 | hp2 | a0011 | c0009 | t0001 | g0180 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03130 | hp1 | a0006 | c0006 | t0001 | g0130 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03130 | hp2 | a0001 | c0001 | t0032 | g0246 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03225 | hp2 | a0004 | c0004 | t0001 | g0040 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0179 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0060 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03516 | hp1 | a0005 | c0005 | t0001 | g0043 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0328 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03654 | hp1 | a0001 | c0001 | t0012 | g0220 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0164 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0290 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03688 | hp2 | a0001 | c0001 | t0013 | g0026 | SAS | STU | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0083 | SAS | BEB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0185 | SAS | BEB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03927 | hp1 | a0009 | c0008 | t0002 | g0221 | SAS | BEB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03927 | hp2 | a0001 | c0001 | t0012 | g0256 | SAS | BEB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | BEB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | STU | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0051 | SAS | STU | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG04184 | hp1 | a0001 | c0001 | t0007 | g0073 | SAS | BEB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0314 | SAS | BEB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0284 | SAS | STU | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG04228 | hp1 | a0001 | c0001 | t0008 | g0312 | SAS | STU | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG04228 | hp2 | a0001 | c0001 | t0012 | g0268 | SAS | STU | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | YRI | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18522 | hp2 | a0001 | c0001 | t0018 | g0244 | AFR | YRI | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18612 | hp1 | a0001 | c0001 | t0015 | g0168 | EAS | CHB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | CHB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18747 | hp1 | a0001 | c0001 | t0009 | g0049 | EAS | CHB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | CHB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | YRI | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18941 | hp2 | a0001 | c0001 | t0006 | g0234 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18945 | hp1 | a0001 | c0001 | t0006 | g0272 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18948 | hp1 | a0001 | c0001 | t0007 | g0096 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18948 | hp2 | a0001 | c0001 | t0027 | g0147 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18952 | hp1 | a0001 | c0001 | t0009 | g0107 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18952 | hp2 | a0001 | c0001 | t0007 | g0108 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18954 | hp1 | a0001 | c0001 | t0008 | g0275 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18959 | hp1 | a0001 | c0001 | t0022 | g0163 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18960 | hp2 | a0001 | c0001 | t0007 | g0144 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18961 | hp2 | a0001 | c0001 | t0006 | g0302 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18965 | hp1 | a0001 | c0001 | t0006 | g0196 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18966 | hp1 | a0001 | c0001 | t0006 | g0310 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18968 | hp2 | a0001 | c0001 | t0029 | g0133 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18971 | hp1 | a0001 | c0001 | t0008 | g0227 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18971 | hp2 | a0001 | c0001 | t0006 | g0305 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18973 | hp1 | a0001 | c0001 | t0009 | g0152 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18974 | hp1 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18974 | hp2 | a0001 | c0001 | t0007 | g0117 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18979 | hp1 | a0001 | c0001 | t0009 | g0050 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18983 | hp1 | a0001 | c0001 | t0010 | g0225 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18984 | hp2 | a0001 | c0001 | t0008 | g0273 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18986 | hp1 | a0001 | c0001 | t0024 | g0151 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0287 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18998 | hp2 | a0001 | c0001 | t0007 | g0115 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19011 | hp1 | a0001 | c0001 | t0008 | g0217 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19012 | hp2 | a0001 | c0001 | t0010 | g0258 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0330 | AFR | LWK | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0095 | AFR | LWK | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | LWK | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0024 | AFR | LWK | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19054 | hp2 | a0001 | c0001 | t0006 | g0277 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19057 | hp2 | a0001 | c0001 | t0012 | g0307 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19058 | hp1 | a0001 | c0001 | t0006 | g0278 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19058 | hp2 | a0001 | c0001 | t0023 | g0142 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19062 | hp1 | a0001 | c0001 | t0006 | g0295 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19063 | hp1 | a0001 | c0001 | t0009 | g0178 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19063 | hp2 | a0001 | c0001 | t0010 | g0261 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19067 | hp1 | a0001 | c0001 | t0007 | g0139 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19068 | hp1 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19074 | hp1 | a0001 | c0001 | t0009 | g0048 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19074 | hp2 | a0001 | c0001 | t0006 | g0271 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19079 | hp2 | a0001 | c0001 | t0034 | g0315 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19080 | hp2 | a0001 | c0001 | t0006 | g0279 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19081 | hp1 | a0001 | c0001 | t0009 | g0153 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19085 | hp1 | a0001 | c0001 | t0016 | g0172 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19085 | hp2 | a0001 | c0001 | t0010 | g0263 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | ASW | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA20129 | hp2 | a0003 | c0003 | t0005 | g0002 | AFR | ASW | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0187 | SAS | GIH | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | GIH | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02109 | hp2 | a0004 | c0004 | t0001 | g0046 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02486 | hp1 | a0002 | c0002 | t0028 | g0105 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0061 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG06807 | hp1 | a0003 | c0003 | t0013 | g0025 | AFR | USA | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| HG06807 | hp2 | a0001 | c0001 | t0019 | g0036 | AFR | USA | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA20300 | hp1 | a0001 | c0001 | t0013 | g0037 | AFR | USA | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | USA | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0010 | g0209 | REF | REF | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0020 | g0023 | REF | REF | MCOLN2_chr1_84920583_85002113 | MCOLN2 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:84931393
|
G | A | 1 | a0007 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1511C>T | p.Ala504Val | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/14 | 1752/3044 | 1511/1701 | 504/566 | chr1 | 84931393 | ||
| chr1:84939555
|
T | G | 1 | a0003 | 9 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
missense_variant&splice_region_variant | MODERATE | c.1108A>C | p.Lys370Gln | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 9/14 | 1349/3044 | 1108/1701 | 370/566 | chr1 | 84939555 | ||
| chr1:84939560
|
T | A | 1 | a0006 | 3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.1103A>T | p.Lys368Ile | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 9/14 | 1344/3044 | 1103/1701 | 368/566 | chr1 | 84939560 | ||
| chr1:84939570
|
T | C | 2 | a0002a0005 | 13 | HG00639.hp2 HG01167.hp2 HG02486.hp1 others(10): Show |
missense_variant | MODERATE | c.1093A>G | p.Met365Val | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 9/14 | 1334/3044 | 1093/1701 | 365/566 | chr1 | 84939570 | ||
| chr1:84940884
|
G | A | 1 | a0006 | 3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.955C>T | p.Arg319Trp | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/14 | 1196/3044 | 955/1701 | 319/566 | chr1 | 84940884 | ||
| chr1:84940979
|
G | C | 1 | a0011 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.860C>G | p.Ala287Gly | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/14 | 1101/3044 | 860/1701 | 287/566 | chr1 | 84940979 | ||
| chr1:84947033
|
T | A | 1 | a0010 | 1 | HG00642.hp2 | missense_variant&splice_region_variant | MODERATE | c.847A>T | p.Thr283Ser | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/14 | 1088/3044 | 847/1701 | 283/566 | chr1 | 84947033 | ||
| chr1:84965616
|
C | T | 1 | a0009 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.170G>A | p.Arg57Gln | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/14 | 411/3044 | 170/1701 | 57/566 | chr1 | 84965616 | ||
| chr1:84965692
|
G | A | 1 | a0008 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.94C>T | p.Arg32Cys | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/14 | 335/3044 | 94/1701 | 32/566 | chr1 | 84965692 | ||
| chr1:84996815
|
C | T | 3 | a0004a0005a0007 | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
missense_variant | MODERATE | c.58G>A | p.Val20Ile | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/14 | 299/3044 | 58/1701 | 20/566 | chr1 | 84996815 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:84929587
|
G | T | 1 | a0010c0010 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.1635C>A | p.Ala545Ala | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/14 | 1876/3044 | 1635/1701 | 545/566 | chr1 | 84929587 | ||
| chr1:84956561
|
G | A | 1 | a0001c0011 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.435C>T | p.Thr145Thr | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/14 | 676/3044 | 435/1701 | 145/566 | chr1 | 84956561 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:84925714
|
A | G | 2 | a0001c0001t0014a0002c0002t0028 | 4 | HG02486.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*971T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 971 | chr1 | 84925714 | |||||
| chr1:84925746
|
C | T | 1 | a0001c0001t0027 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*939G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 939 | chr1 | 84925746 | |||||
| chr1:84925807
|
T | C | 1 | a0001c0001t0034 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*878A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 878 | chr1 | 84925807 | |||||
| chr1:84925881
|
A | C | 3 | a0001c0001t0010a0001c0001t0015a0001c0001t0029 | 9 | HG00673.hp2 HG01981.hp2 NA18612.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*804T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 804 | chr1 | 84925881 | |||||
| chr1:84925892
|
A | AT | 11 | a0001c0001t0006a0001c0001t0007a0001c0001t0014others(8): Show | 42 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*792dupA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 792 | chr1 | 84925892 | |||||
| chr1:84925892
|
AT | A | 4 | a0001c0001t0008a0001c0001t0009a0001c0001t0012others(1): Show | 24 | HG01928.hp2 HG01943.hp1 HG01978.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*792delA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 792 | chr1 | 84925892 | |||||
| chr1:84925899
|
T | TTG | 2 | a0001c0001t0010a0001c0001t0015 | 8 | HG00673.hp2 HG01981.hp2 NA18612.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*785_*786insCA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 785 | chr1 | 84925899 | |||||
| chr1:84926013
|
C | T | 2 | a0001c0001t0032a0001c0001t0035 | 2 | HG02572.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*672G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 672 | chr1 | 84926013 | |||||
| chr1:84926046
|
C | T | 2 | a0001c0001t0023a0001c0001t0030 | 2 | HG01257.hp1 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*639G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 639 | chr1 | 84926046 | |||||
| chr1:84926215
|
C | T | 1 | a0001c0001t0027 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*470G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 470 | chr1 | 84926215 | |||||
| chr1:84926216
|
A | G | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | 349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*469T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 469 | chr1 | 84926216 | |||||
| chr1:84926338
|
C | T | 1 | a0001c0001t0022 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*347G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 347 | chr1 | 84926338 | |||||
| chr1:84926374
|
G | A | 4 | a0001c0001t0017a0001c0001t0018a0001c0001t0030others(1): Show | 6 | HG00280.hp1 HG01169.hp1 HG01257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*311C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 311 | chr1 | 84926374 | |||||
| chr1:84926381
|
C | G | 3 | a0001c0001t0019a0001c0001t0021a0001c0001t0026 | 3 | HG01993.hp2 HG02647.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*304G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 304 | chr1 | 84926381 | |||||
| chr1:84926478
|
A | G | 1 | a0006c0006t0025 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*207T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 207 | chr1 | 84926478 | |||||
| chr1:84926641
|
C | T | 17 | a0001c0001t0003a0001c0001t0004a0001c0001t0012others(14): Show | 93 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*44G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 44 | chr1 | 84926641 | |||||
| chr1:84996899
|
C | G | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(13): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
5_prime_UTR_variant | MODIFIER | c.-27G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/14 | 27 | chr1 | 84996899 | |||||
| chr1:84996969
|
G | T | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(13): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
5_prime_UTR_variant | MODIFIER | c.-97C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/14 | 97 | chr1 | 84996969 | |||||
| chr1:84996982
|
T | G | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(13): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
5_prime_UTR_variant | MODIFIER | c.-110A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/14 | 110 | chr1 | 84996982 | |||||
| chr1:84997067
|
T | C | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
5_prime_UTR_variant | MODIFIER | c.-195A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/14 | 195 | chr1 | 84997067 | |||||
| chr1:84997089
|
G | C | 1 | a0001c0001t0011 | 5 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-217C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/14 | 217 | chr1 | 84997089 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:84926933
|
A | C | 150 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(147): Show | 158 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1665-212T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84926933 | ||||||
| chr1:84926977
|
G | A | 1 | a0001c0001t0003g0202 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1665-256C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84926977 | ||||||
| chr1:84927043
|
G | A | 1 | a0001c0001t0003g0186 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1665-322C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927043 | ||||||
| chr1:84927157
|
T | G | 21 | a0001c0001t0001g0138a0001c0001t0001g0150a0001c0001t0002g0322others(18): Show | 21 | HG00558.hp1 HG00609.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1665-436A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927157 | ||||||
| chr1:84927192
|
T | C | 1 | a0001c0001t0002g0313 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1665-471A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927192 | ||||||
| chr1:84927192
|
T | G | 11 | a0001c0001t0002g0308a0001c0001t0005g0034a0002c0002t0001g0052others(8): Show | 11 | HG02486.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1665-471A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927192 | ||||||
| chr1:84927204
|
TA | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 173 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.1665-484delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927204 | ||||||
| chr1:84927205
|
A | T | 3 | a0002c0002t0001g0058a0002c0002t0002g0009a0002c0002t0002g0236 | 4 | HG01167.hp2 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1665-484T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927205 | ||||||
| chr1:84927228
|
T | C | 1 | a0001c0001t0002g0265 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1665-507A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927228 | ||||||
| chr1:84927271
|
T | TG | 6 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0010g0225others(3): Show | 6 | HG00673.hp2 NA18612.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1665-551dupC | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927271 | ||||||
| chr1:84927347
|
T | A | 1 | a0001c0001t0007g0144 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1665-626A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927347 | ||||||
| chr1:84927489
|
A | T | 12 | a0001c0001t0001g0075a0001c0001t0002g0242a0001c0001t0002g0276others(9): Show | 14 | HG00280.hp2 HG00639.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1665-768T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927489 | ||||||
| chr1:84927498
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1665-777C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927498 | ||||||
| chr1:84927752
|
T | C | 1 | a0001c0001t0005g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1665-1031A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927752 | ||||||
| chr1:84927788
|
T | G | 1 | a0001c0001t0014g0019 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1665-1067A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927788 | ||||||
| chr1:84927809
|
G | A | 15 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0076others(12): Show | 17 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1665-1088C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927809 | ||||||
| chr1:84928465
|
T | C | 79 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0064others(76): Show | 81 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1664+1093A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928465 | ||||||
| chr1:84928525
|
T | G | 5 | a0001c0001t0001g0082a0001c0001t0003g0213a0001c0001t0004g0097others(2): Show | 5 | HG01074.hp1 HG01175.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.1664+1033A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928525 | ||||||
| chr1:84928575
|
T | G | 35 | a0001c0001t0001g0003a0001c0001t0001g0090a0001c0001t0001g0110others(32): Show | 37 | HG00323.hp1 HG00735.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.1664+983A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928575 | ||||||
| chr1:84928603
|
T | C | 8 | a0001c0001t0002g0247a0001c0001t0002g0296a0001c0001t0005g0024others(5): Show | 8 | HG02559.hp2 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1664+955A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928603 | ||||||
| chr1:84928622
|
A | G | 7 | a0001c0001t0001g0067a0001c0001t0001g0121a0001c0001t0004g0079others(4): Show | 7 | HG02280.hp2 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1664+936T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928622 | ||||||
| chr1:84928665
|
A | C | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1664+893T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928665 | ||||||
| chr1:84928683
|
A | C | 60 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0064others(57): Show | 60 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1664+875T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928683 | ||||||
| chr1:84928723
|
T | A | 1 | a0001c0001t0005g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1664+835A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928723 | ||||||
| chr1:84928815
|
T | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0055a0001c0001t0001g0080others(75): Show | 81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1664+743A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928815 | ||||||
| chr1:84928942
|
T | G | 2 | a0001c0001t0004g0092a0001c0001t0010g0258 | 2 | NA18999.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1664+616A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928942 | ||||||
| chr1:84929041
|
G | C | 1 | a0001c0001t0004g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1664+517C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84929041 | ||||||
| chr1:84929064
|
C | T | 5 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0069others(2): Show | 5 | HG02055.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1664+494G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84929064 | ||||||
| chr1:84929340
|
A | G | 1 | a0001c0001t0003g0324 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1664+218T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84929340 | ||||||
| chr1:84929361
|
G | A | 1 | a0002c0002t0002g0243 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1664+197C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84929361 | ||||||
| chr1:84929788
|
A | C | 1 | a0001c0001t0001g0067 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1543-109T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84929788 | ||||||
| chr1:84929933
|
T | A | 172 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0053others(169): Show | 177 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.1543-254A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84929933 | ||||||
| chr1:84929933
|
T | TA | 9 | a0002c0002t0001g0061a0002c0002t0001g0065a0002c0002t0001g0122others(6): Show | 9 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1543-255dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84929933 | ||||||
| chr1:84929933
|
T | TAA | 15 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0076others(12): Show | 17 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1543-256_1543-255d others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84929933 | ||||||
| chr1:84929934
|
A | T | 10 | a0001c0001t0001g0169a0001c0001t0002g0257a0001c0001t0004g0148others(7): Show | 11 | HG01928.hp1 HG01934.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1543-255T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84929934 | ||||||
| chr1:84929937
|
A | G | 3 | a0006c0006t0001g0130a0006c0006t0003g0327a0006c0006t0025g0131 | 3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1543-258T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84929937 | ||||||
| chr1:84930042
|
C | A | 24 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0062others(21): Show | 25 | HG01981.hp1 HG01993.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1543-363G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930042 | ||||||
| chr1:84930139
|
T | C | 1 | a0001c0001t0002g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1543-460A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930139 | ||||||
| chr1:84930178
|
G | A | 16 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(13): Show | 18 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1543-499C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930178 | ||||||
| chr1:84930269
|
T | A | 30 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(27): Show | 31 | HG00280.hp2 HG00741.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1543-590A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930269 | ||||||
| chr1:84930269
|
T | TA | 11 | a0001c0001t0002g0247a0001c0001t0002g0296a0001c0001t0005g0032others(8): Show | 11 | HG00741.hp2 HG01099.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1543-591dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930269 | ||||||
| chr1:84930269
|
TA | T | 11 | a0001c0001t0002g0224a0001c0001t0005g0038a0003c0003t0001g0086others(8): Show | 12 | HG00642.hp2 HG01884.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1543-591delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930269 | ||||||
| chr1:84930270
|
A | T | 2 | a0001c0001t0001g0054a0001c0001t0018g0223 | 2 | HG03017.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1543-591T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930270 | ||||||
| chr1:84930337
|
C | G | 2 | a0001c0001t0002g0319a0004c0004t0001g0040 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1543-658G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930337 | ||||||
| chr1:84930348
|
T | A | 36 | a0001c0001t0001g0003a0001c0001t0001g0090a0001c0001t0001g0110others(33): Show | 38 | HG00323.hp1 HG00735.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.1543-669A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930348 | ||||||
| chr1:84930357
|
T | G | 1 | a0001c0001t0001g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1543-678A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930357 | ||||||
| chr1:84930456
|
C | T | 1 | a0001c0001t0011g0335 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1543-777G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930456 | ||||||
| chr1:84930475
|
T | C | 219 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0053others(216): Show | 227 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.1543-796A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930475 | ||||||
| chr1:84930511
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1543-832C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930511 | ||||||
| chr1:84930759
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1542+603C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930759 | ||||||
| chr1:84930907
|
A | T | 6 | a0001c0001t0002g0308a0001c0001t0002g0319a0001c0001t0002g0320others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1542+455T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930907 | ||||||
| chr1:84930953
|
T | C | 1 | a0010c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1542+409A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930953 | ||||||
| chr1:84930975
|
T | C | 1 | a0010c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1542+387A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930975 | ||||||
| chr1:84931012
|
C | T | 10 | a0001c0001t0005g0038a0003c0003t0001g0086a0003c0003t0001g0095others(7): Show | 11 | HG00642.hp2 HG01884.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1542+350G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84931012 | ||||||
| chr1:84931038
|
T | G | 1 | a0001c0001t0005g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1542+324A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84931038 | ||||||
| chr1:84931095
|
A | G | 1 | a0010c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1542+267T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84931095 | ||||||
| chr1:84931115
|
A | ACTTACCC others(13): Show |
1 | a0001c0001t0007g0144 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1542+227_1542+246d others(22): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84931115 | ||||||
| chr1:84931117
|
T | C | 33 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0062others(30): Show | 34 | HG00639.hp2 HG01981.hp1 HG01993.hp1 others(31): Show |
intron_variant | MODIFIER | c.1542+245A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84931117 | ||||||
| chr1:84931207
|
A | G | 1 | a0001c0001t0002g0212 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1542+155T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84931207 | ||||||
| chr1:84931603
|
G | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0055a0001c0001t0001g0080others(75): Show | 81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-35C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84931603 | ||||||
| chr1:84931650
|
A | G | 8 | a0001c0001t0002g0247a0001c0001t0002g0296a0001c0001t0005g0024others(5): Show | 8 | HG02559.hp2 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1336-82T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84931650 | ||||||
| chr1:84932010
|
C | A | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1336-442G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932010 | ||||||
| chr1:84932029
|
A | AAC | 28 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0066others(25): Show | 31 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.1336-463_1336-462d others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932029 | ||||||
| chr1:84932029
|
A | AACAC | 9 | a0001c0001t0001g0062a0001c0001t0001g0119a0001c0001t0001g0123others(6): Show | 9 | HG02055.hp1 HG02965.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.1336-465_1336-462d others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932029 | ||||||
| chr1:84932029
|
A | AACACAC | 6 | a0002c0002t0001g0052a0002c0002t0001g0122a0002c0002t0028g0105others(3): Show | 6 | HG02486.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1336-467_1336-462d others(8): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932029 | ||||||
| chr1:84932029
|
AAC | A | 83 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0064others(80): Show | 84 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.1336-463_1336-462d others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932029 | ||||||
| chr1:84932439
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1336-871G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932439 | ||||||
| chr1:84932592
|
CT | C | 21 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(18): Show | 24 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1336-1025delA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932592 | ||||||
| chr1:84932651
|
T | C | 23 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(20): Show | 26 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1336-1083A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932651 | ||||||
| chr1:84932874
|
C | G | 1 | a0001c0001t0007g0051 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1336-1306G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932874 | ||||||
| chr1:84933024
|
T | C | 1 | a0001c0001t0008g0275 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1336-1456A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933024 | ||||||
| chr1:84933089
|
C | A | 9 | a0002c0002t0001g0052a0002c0002t0001g0061a0002c0002t0001g0065others(6): Show | 9 | HG00639.hp2 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1336-1521G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933089 | ||||||
| chr1:84933296
|
C | T | 4 | a0001c0001t0002g0308a0001c0001t0002g0320a0004c0004t0001g0046others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1336-1728G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933296 | ||||||
| chr1:84933370
|
C | T | 3 | a0002c0002t0001g0058a0002c0002t0002g0009a0002c0002t0002g0236 | 4 | HG01167.hp2 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1336-1802G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933370 | ||||||
| chr1:84933533
|
T | C | 3 | a0001c0001t0002g0233a0001c0001t0002g0319a0004c0004t0001g0040 | 3 | HG02258.hp1 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1336-1965A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933533 | ||||||
| chr1:84933545
|
G | C | 221 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0053others(218): Show | 229 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.1336-1977C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933545 | ||||||
| chr1:84933649
|
C | T | 1 | a0001c0001t0005g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1336-2081G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933649 | ||||||
| chr1:84933684
|
T | C | 1 | a0001c0001t0003g0259 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1336-2116A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933684 | ||||||
| chr1:84933744
|
T | C | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1336-2176A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933744 | ||||||
| chr1:84933802
|
A | G | 4 | a0001c0001t0002g0308a0001c0001t0002g0320a0004c0004t0001g0046others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1336-2234T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933802 | ||||||
| chr1:84933927
|
C | A | 8 | a0003c0003t0001g0086a0003c0003t0001g0095a0003c0003t0005g0002others(5): Show | 9 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1336-2359G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933927 | ||||||
| chr1:84934076
|
T | C | 1 | a0001c0001t0005g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1336-2508A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934076 | ||||||
| chr1:84934098
|
A | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0055a0001c0001t0001g0080others(75): Show | 81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-2530T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934098 | ||||||
| chr1:84934157
|
A | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0055a0001c0001t0001g0080others(75): Show | 81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-2589T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934157 | ||||||
| chr1:84934317
|
TCCATAAA others(6): Show |
T | 181 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0053others(178): Show | 186 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1336-2762_1336-275 others(17): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934317 | ||||||
| chr1:84934343
|
T | C | 4 | a0001c0001t0002g0308a0001c0001t0002g0320a0004c0004t0001g0046others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1336-2775A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934343 | ||||||
| chr1:84934383
|
A | G | 1 | a0001c0001t0003g0266 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1336-2815T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934383 | ||||||
| chr1:84934431
|
C | A | 85 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0057others(82): Show | 86 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1336-2863G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934431 | ||||||
| chr1:84934499
|
C | T | 177 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0053others(174): Show | 182 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.1336-2931G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934499 | ||||||
| chr1:84934574
|
GCA | G | 78 | a0001c0001t0001g0003a0001c0001t0001g0055a0001c0001t0001g0080others(75): Show | 81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-3008_1336-300 others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934574 | ||||||
| chr1:84934718
|
C | T | 1 | a0001c0001t0003g0206 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1335+3037G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934718 | ||||||
| chr1:84934880
|
T | C | 8 | a0001c0001t0002g0247a0001c0001t0002g0296a0001c0001t0005g0024others(5): Show | 8 | HG02559.hp2 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1335+2875A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934880 | ||||||
| chr1:84935055
|
C | T | 3 | a0002c0002t0001g0058a0002c0002t0002g0009a0002c0002t0002g0236 | 4 | HG01167.hp2 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1335+2700G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935055 | ||||||
| chr1:84935152
|
T | C | 6 | a0001c0001t0002g0308a0001c0001t0002g0319a0001c0001t0002g0320others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1335+2603A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935152 | ||||||
| chr1:84935155
|
G | A | 1 | a0001c0001t0003g0210 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1335+2600C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935155 | ||||||
| chr1:84935210
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1335+2545G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935210 | ||||||
| chr1:84935233
|
A | C | 1 | a0001c0001t0003g0213 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1335+2522T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935233 | ||||||
| chr1:84935252
|
C | T | 140 | a0001c0001t0001g0003a0001c0001t0001g0055a0001c0001t0001g0057others(137): Show | 143 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.1335+2503G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935252 | ||||||
| chr1:84935363
|
A | C | 1 | a0001c0001t0002g0198 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1335+2392T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935363 | ||||||
| chr1:84935426
|
A | C | 1 | a0001c0001t0007g0170 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1335+2329T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935426 | ||||||
| chr1:84935799
|
T | C | 16 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(13): Show | 18 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1335+1956A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935799 | ||||||
| chr1:84935842
|
T | G | 2 | a0001c0001t0001g0177a0001c0001t0029g0133 | 2 | NA18968.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1335+1913A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935842 | ||||||
| chr1:84935880
|
T | G | 1 | a0001c0001t0006g0283 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1335+1875A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935880 | ||||||
| chr1:84936033
|
C | T | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1335+1722G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936033 | ||||||
| chr1:84936035
|
G | T | 62 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0064others(59): Show | 62 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1335+1720C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936035 | ||||||
| chr1:84936110
|
C | T | 1 | a0001c0001t0002g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1335+1645G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936110 | ||||||
| chr1:84936187
|
G | C | 1 | a0004c0004t0001g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1335+1568C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936187 | ||||||
| chr1:84936559
|
A | C | 79 | a0001c0001t0001g0003a0001c0001t0001g0055a0001c0001t0001g0080others(76): Show | 82 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1335+1196T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936559 | ||||||
| chr1:84936561
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1335+1194T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936561 | ||||||
| chr1:84936790
|
A | G | 1 | a0001c0001t0026g0085 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1335+965T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936790 | ||||||
| chr1:84936806
|
C | T | 1 | a0001c0001t0003g0311 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1335+949G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936806 | ||||||
| chr1:84936961
|
C | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0080a0001c0001t0001g0090others(34): Show | 39 | HG00323.hp1 HG00735.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.1335+794G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936961 | ||||||
| chr1:84937189
|
C | T | 1 | a0001c0001t0005g0035 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1335+566G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937189 | ||||||
| chr1:84937250
|
A | G | 1 | a0001c0001t0007g0115 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1335+505T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937250 | ||||||
| chr1:84937283
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1335+472C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937283 | ||||||
| chr1:84937314
|
A | G | 105 | a0001c0001t0001g0003a0001c0001t0001g0055a0001c0001t0001g0080others(102): Show | 109 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1335+441T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937314 | ||||||
| chr1:84937429
|
C | T | 3 | a0002c0002t0001g0058a0002c0002t0002g0009a0002c0002t0002g0236 | 4 | HG01167.hp2 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1335+326G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937429 | ||||||
| chr1:84937462
|
C | T | 213 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0053others(210): Show | 219 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.1335+293G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937462 | ||||||
| chr1:84937491
|
C | T | 1 | a0002c0002t0028g0105 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1335+264G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937491 | ||||||
| chr1:84937492
|
G | A | 8 | a0003c0003t0001g0086a0003c0003t0001g0095a0003c0003t0005g0002others(5): Show | 9 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1335+263C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937492 | ||||||
| chr1:84937542
|
T | C | 2 | a0001c0001t0002g0325a0001c0001t0002g0329 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1335+213A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937542 | ||||||
| chr1:84937661
|
G | A | 1 | a0001c0001t0002g0309 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1335+94C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937661 | ||||||
| chr1:84937887
|
A | T | 8 | a0001c0001t0001g0116a0001c0001t0001g0120a0001c0001t0001g0121others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1213-10T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 10/13 | chr1 | 84937887 | ||||||
| chr1:84938672
|
C | T | 8 | a0001c0001t0002g0212a0001c0001t0006g0231a0001c0001t0006g0286others(5): Show | 8 | HG02056.hp1 HG02056.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1111-590G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 9/13 | chr1 | 84938672 | ||||||
| chr1:84939007
|
G | T | 1 | a0003c0003t0001g0095 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1110+546C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 9/13 | chr1 | 84939007 | ||||||
| chr1:84939078
|
G | A | 1 | a0001c0001t0001g0006 | 2 | NA18964.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1110+475C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 9/13 | chr1 | 84939078 | ||||||
| chr1:84939115
|
T | G | 1 | a0001c0001t0017g0100 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1110+438A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 9/13 | chr1 | 84939115 | ||||||
| chr1:84939543
|
C | T | 8 | a0001c0001t0002g0247a0001c0001t0002g0296a0001c0001t0005g0024others(5): Show | 8 | HG02559.hp2 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1110+10G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 9/13 | chr1 | 84939543 | ||||||
| chr1:84939706
|
T | G | 24 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0062others(21): Show | 25 | HG01981.hp1 HG01993.hp1 HG02055.hp1 others(22): Show |
splice_region_variant&intron_variant | LOW | c.961-4A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84939706 | ||||||
| chr1:84939911
|
T | G | 3 | a0006c0006t0001g0130a0006c0006t0003g0327a0006c0006t0025g0131 | 3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.961-209A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84939911 | ||||||
| chr1:84940003
|
C | T | 7 | a0003c0003t0001g0095a0003c0003t0005g0002a0003c0003t0005g0028others(4): Show | 8 | HG01884.hp2 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-301G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940003 | ||||||
| chr1:84940007
|
A | G | 3 | a0006c0006t0001g0130a0006c0006t0003g0327a0006c0006t0025g0131 | 3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.961-305T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940007 | ||||||
| chr1:84940041
|
C | A | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.961-339G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940041 | ||||||
| chr1:84940101
|
C | T | 18 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0069others(15): Show | 18 | HG02055.hp1 HG02055.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.961-399G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940101 | ||||||
| chr1:84940102
|
G | A | 3 | a0006c0006t0001g0130a0006c0006t0003g0327a0006c0006t0025g0131 | 3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.961-400C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940102 | ||||||
| chr1:84940156
|
C | G | 2 | a0006c0006t0001g0130a0006c0006t0025g0131 | 2 | HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.961-454G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940156 | ||||||
| chr1:84940204
|
A | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0053others(152): Show | 163 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.961-502T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940204 | ||||||
| chr1:84940211
|
A | G | 77 | a0001c0001t0001g0003a0001c0001t0001g0055a0001c0001t0001g0080others(74): Show | 80 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.961-509T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940211 | ||||||
| chr1:84940360
|
T | C | 1 | a0001c0001t0002g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.960+519A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940360 | ||||||
| chr1:84940390
|
C | A | 1 | a0001c0001t0002g0326 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.960+489G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940390 | ||||||
| chr1:84941100
|
G | C | 1 | a0001c0001t0003g0241 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.848-109C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941100 | ||||||
| chr1:84941119
|
T | C | 8 | a0001c0001t0002g0247a0001c0001t0002g0296a0001c0001t0005g0024others(5): Show | 8 | HG02559.hp2 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-128A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941119 | ||||||
| chr1:84941268
|
G | C | 3 | a0006c0006t0001g0130a0006c0006t0003g0327a0006c0006t0025g0131 | 3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.848-277C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941268 | ||||||
| chr1:84941278
|
C | T | 3 | a0006c0006t0001g0130a0006c0006t0003g0327a0006c0006t0025g0131 | 3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.848-287G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941278 | ||||||
| chr1:84941307
|
T | C | 3 | a0006c0006t0001g0130a0006c0006t0003g0327a0006c0006t0025g0131 | 3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.848-316A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941307 | ||||||
| chr1:84941315
|
T | C | 18 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(15): Show | 21 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.848-324A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941315 | ||||||
| chr1:84941369
|
C | A | 34 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0062others(31): Show | 35 | HG01981.hp1 HG01993.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.848-378G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941369 | ||||||
| chr1:84941415
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.848-424A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941415 | ||||||
| chr1:84941461
|
C | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 191 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.848-470G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941461 | ||||||
| chr1:84941462
|
G | A | 1 | a0001c0001t0007g0164 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.848-471C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941462 | ||||||
| chr1:84941501
|
C | CA | 9 | a0002c0002t0001g0052a0002c0002t0001g0061a0002c0002t0001g0065others(6): Show | 9 | HG00639.hp2 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.848-511dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941501 | ||||||
| chr1:84941508
|
C | G | 1 | a0001c0001t0002g0276 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.848-517G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941508 | ||||||
| chr1:84941565
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 207 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.848-574A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941565 | ||||||
| chr1:84941774
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.848-783G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941774 | ||||||
| chr1:84941926
|
T | C | 12 | a0001c0001t0001g0090a0001c0001t0001g0110a0001c0001t0002g0191others(9): Show | 12 | HG00323.hp1 HG01106.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.848-935A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941926 | ||||||
| chr1:84941963
|
C | G | 3 | a0005c0005t0001g0042a0005c0005t0001g0043a0005c0005t0001g0044 | 3 | HG02615.hp2 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.848-972G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941963 | ||||||
| chr1:84941965
|
C | T | 18 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(15): Show | 21 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.848-974G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941965 | ||||||
| chr1:84941966
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 207 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.848-975T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941966 | ||||||
| chr1:84942061
|
T | A | 3 | a0001c0001t0001g0150a0001c0001t0001g0160a0001c0001t0001g0162 | 3 | HG01243.hp1 NA18943.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.848-1070A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942061 | ||||||
| chr1:84942180
|
A | G | 39 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(36): Show | 42 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.848-1189T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942180 | ||||||
| chr1:84942280
|
C | T | 1 | a0001c0001t0023g0142 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.848-1289G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942280 | ||||||
| chr1:84942303
|
G | C | 61 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0064others(58): Show | 61 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.848-1312C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942303 | ||||||
| chr1:84942348
|
C | T | 1 | a0001c0001t0002g0229 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.848-1357G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942348 | ||||||
| chr1:84942447
|
G | A | 1 | a0001c0001t0005g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.848-1456C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942447 | ||||||
| chr1:84942583
|
TC | T | 62 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0064others(59): Show | 62 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.848-1593delG | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942583 | ||||||
| chr1:84942641
|
G | A | 62 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0064others(59): Show | 62 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.848-1650C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942641 | ||||||
| chr1:84942849
|
AC | A | 9 | a0001c0001t0002g0247a0001c0001t0002g0296a0001c0001t0005g0024others(6): Show | 9 | HG00642.hp2 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.848-1859delG | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942849 | ||||||
| chr1:84942933
|
G | T | 50 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0064others(47): Show | 50 | HG00323.hp2 HG00558.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.848-1942C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942933 | ||||||
| chr1:84943353
|
T | G | 114 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0057others(111): Show | 116 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.848-2362A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84943353 | ||||||
| chr1:84943372
|
G | A | 23 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(20): Show | 26 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.848-2381C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84943372 | ||||||
| chr1:84943508
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.848-2517C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84943508 | ||||||
| chr1:84943582
|
CCA | C | 10 | a0001c0001t0002g0247a0001c0001t0002g0296a0001c0001t0002g0319others(7): Show | 10 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.848-2593_848-2592d others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84943582 | ||||||
| chr1:84943670
|
G | A | 1 | a0001c0001t0007g0115 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.848-2679C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84943670 | ||||||
| chr1:84944261
|
G | A | 1 | a0001c0001t0006g0286 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.847+2772C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944261 | ||||||
| chr1:84944347
|
A | G | 8 | a0001c0001t0005g0038a0003c0003t0001g0095a0003c0003t0005g0002others(5): Show | 9 | HG01884.hp2 HG02818.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.847+2686T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944347 | ||||||
| chr1:84944378
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0174a0001c0001t0004g0146 | 3 | HG00558.hp2 NA18960.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.847+2655G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944378 | ||||||
| chr1:84944389
|
C | T | 1 | a0001c0001t0003g0208 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.847+2644G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944389 | ||||||
| chr1:84944392
|
G | A | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.847+2641C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944392 | ||||||
| chr1:84944479
|
G | GC | 14 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(11): Show | 15 | HG00642.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.847+2553dupG | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944479 | ||||||
| chr1:84944533
|
A | AAAAG | 9 | a0001c0001t0001g0169a0001c0001t0004g0148a0001c0001t0006g0271others(6): Show | 10 | HG01928.hp1 HG01943.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.847+2496_847+2499d others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944533 | ||||||
| chr1:84944533
|
A | G | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.847+2500T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944533 | ||||||
| chr1:84944533
|
AAAAG | A | 14 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(11): Show | 15 | HG00642.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.847+2496_847+2499d others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944533 | ||||||
| chr1:84944559
|
A | G | 32 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(29): Show | 35 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.847+2474T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944559 | ||||||
| chr1:84944591
|
C | T | 1 | a0001c0001t0003g0190 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.847+2442G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944591 | ||||||
| chr1:84944608
|
C | T | 2 | a0001c0001t0002g0205a0001c0001t0003g0206 | 2 | HG01952.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.847+2425G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944608 | ||||||
| chr1:84944657
|
C | T | 1 | a0010c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.847+2376G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944657 | ||||||
| chr1:84944857
|
A | C | 1 | a0001c0001t0001g0067 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.847+2176T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944857 | ||||||
| chr1:84944861
|
C | T | 82 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0057others(79): Show | 83 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+2172G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944861 | ||||||
| chr1:84945071
|
TA | T | 55 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(52): Show | 59 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.847+1961delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84945071 | ||||||
| chr1:84945136
|
T | C | 1 | a0001c0001t0003g0240 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.847+1897A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84945136 | ||||||
| chr1:84945366
|
T | TC | 18 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(15): Show | 21 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.847+1666dupG | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84945366 | ||||||
| chr1:84945674
|
T | C | 14 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(11): Show | 15 | HG00642.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.847+1359A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84945674 | ||||||
| chr1:84945748
|
T | C | 9 | a0002c0002t0001g0052a0002c0002t0001g0061a0002c0002t0001g0065others(6): Show | 9 | HG00639.hp2 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+1285A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84945748 | ||||||
| chr1:84946002
|
G | A | 14 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(11): Show | 15 | HG00642.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.847+1031C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946002 | ||||||
| chr1:84946038
|
T | C | 14 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(11): Show | 15 | HG00642.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.847+995A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946038 | ||||||
| chr1:84946123
|
C | T | 1 | a0001c0001t0003g0008 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.847+910G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946123 | ||||||
| chr1:84946320
|
G | A | 1 | a0002c0002t0002g0243 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.847+713C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946320 | ||||||
| chr1:84946448
|
A | G | 14 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(11): Show | 15 | HG00642.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.847+585T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946448 | ||||||
| chr1:84946464
|
T | C | 1 | a0001c0001t0003g0241 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.847+569A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946464 | ||||||
| chr1:84946482
|
T | A | 2 | a0001c0001t0001g0166a0001c0001t0002g0284 | 2 | HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.847+551A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946482 | ||||||
| chr1:84946607
|
T | C | 13 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(10): Show | 14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.847+426A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946607 | ||||||
| chr1:84946753
|
C | T | 82 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0057others(79): Show | 83 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+280G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946753 | ||||||
| chr1:84946778
|
C | T | 13 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(10): Show | 14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.847+255G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946778 | ||||||
| chr1:84946940
|
T | C | 13 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(10): Show | 14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.847+93A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946940 | ||||||
| chr1:84947306
|
C | CCACA | 16 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(13): Show | 18 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.748-178_748-175dup others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947306 | ||||||
| chr1:84947306
|
C | CCACACA | 11 | a0002c0002t0001g0052a0002c0002t0001g0058a0002c0002t0001g0061others(8): Show | 12 | HG01167.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.748-180_748-175dup others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947306 | ||||||
| chr1:84947306
|
CCA | C | 24 | a0001c0001t0002g0198a0001c0001t0002g0233a0001c0001t0002g0247others(21): Show | 25 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.748-176_748-175del others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947306 | ||||||
| chr1:84947329
|
C | A | 13 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(10): Show | 14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-197G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947329 | ||||||
| chr1:84947329
|
C | CACACAT | 3 | a0006c0006t0001g0130a0006c0006t0003g0327a0006c0006t0025g0131 | 3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.748-198_748-197ins others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947329 | ||||||
| chr1:84947518
|
A | G | 13 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(10): Show | 14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-386T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947518 | ||||||
| chr1:84947592
|
C | A | 47 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(44): Show | 51 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.748-460G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947592 | ||||||
| chr1:84947651
|
G | A | 13 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(10): Show | 14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-519C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947651 | ||||||
| chr1:84947673
|
C | T | 2 | a0003c0003t0001g0095a0003c0003t0013g0025 | 2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.748-541G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947673 | ||||||
| chr1:84947697
|
G | A | 36 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(33): Show | 40 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.748-565C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947697 | ||||||
| chr1:84947793
|
TTG | T | 13 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(10): Show | 14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-663_748-662del others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947793 | ||||||
| chr1:84947964
|
G | C | 13 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(10): Show | 14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-832C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947964 | ||||||
| chr1:84948082
|
T | C | 137 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0057others(134): Show | 142 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.748-950A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948082 | ||||||
| chr1:84948223
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.748-1091G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948223 | ||||||
| chr1:84948308
|
C | T | 19 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(16): Show | 22 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.748-1176G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948308 | ||||||
| chr1:84948403
|
A | C | 13 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(10): Show | 14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-1271T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948403 | ||||||
| chr1:84948428
|
T | C | 3 | a0006c0006t0001g0130a0006c0006t0003g0327a0006c0006t0025g0131 | 3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.748-1296A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948428 | ||||||
| chr1:84948440
|
T | G | 10 | a0001c0001t0002g0247a0001c0001t0002g0296a0001c0001t0002g0319others(7): Show | 10 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.748-1308A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948440 | ||||||
| chr1:84948445
|
C | A | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.748-1313G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948445 | ||||||
| chr1:84948464
|
T | C | 11 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0069others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.748-1332A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948464 | ||||||
| chr1:84948583
|
A | G | 13 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(10): Show | 14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-1451T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948583 | ||||||
| chr1:84948853
|
C | T | 11 | a0001c0001t0002g0233a0001c0001t0002g0247a0001c0001t0002g0296others(8): Show | 11 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.748-1721G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948853 | ||||||
| chr1:84948854
|
G | A | 1 | a0003c0003t0001g0095 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.748-1722C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948854 | ||||||
| chr1:84949001
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.748-1869C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949001 | ||||||
| chr1:84949008
|
C | T | 137 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0057others(134): Show | 142 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.748-1876G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949008 | ||||||
| chr1:84949010
|
A | T | 1 | a0010c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.748-1878T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949010 | ||||||
| chr1:84949044
|
C | T | 1 | a0001c0001t0003g0185 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.748-1912G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949044 | ||||||
| chr1:84949091
|
C | G | 13 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(10): Show | 14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-1959G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949091 | ||||||
| chr1:84949130
|
G | A | 1 | a0010c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.748-1998C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949130 | ||||||
| chr1:84949157
|
A | G | 1 | a0001c0001t0004g0181 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.748-2025T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949157 | ||||||
| chr1:84949157
|
A | T | 10 | a0001c0001t0002g0247a0001c0001t0002g0296a0001c0001t0002g0319others(7): Show | 10 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.748-2025T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949157 | ||||||
| chr1:84949335
|
G | A | 47 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(44): Show | 51 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.748-2203C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949335 | ||||||
| chr1:84949361
|
G | A | 5 | a0001c0001t0002g0233a0001c0001t0002g0308a0004c0004t0001g0039others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-2229C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949361 | ||||||
| chr1:84949366
|
C | T | 5 | a0001c0001t0005g0017a0001c0001t0005g0022a0001c0001t0014g0015others(2): Show | 5 | HG02257.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-2234G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949366 | ||||||
| chr1:84949421
|
G | A | 13 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(10): Show | 14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-2289C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949421 | ||||||
| chr1:84949455
|
G | A | 90 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0057others(87): Show | 91 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.748-2323C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949455 | ||||||
| chr1:84949482
|
C | CA | 5 | a0001c0001t0001g0082a0001c0001t0003g0213a0001c0001t0004g0097others(2): Show | 5 | HG01074.hp1 HG01175.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-2351dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949482 | ||||||
| chr1:84949482
|
CA | C | 12 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(9): Show | 13 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.748-2351delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949482 | ||||||
| chr1:84949497
|
T | C | 55 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(52): Show | 59 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.748-2365A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949497 | ||||||
| chr1:84949747
|
G | T | 13 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(10): Show | 14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.747+2496C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949747 | ||||||
| chr1:84950030
|
T | C | 1 | a0001c0001t0006g0287 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.747+2213A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84950030 | ||||||
| chr1:84950115
|
A | T | 90 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0057others(87): Show | 91 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.747+2128T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84950115 | ||||||
| chr1:84950389
|
A | C | 13 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(10): Show | 14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.747+1854T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84950389 | ||||||
| chr1:84950405
|
T | G | 1 | a0001c0001t0008g0211 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.747+1838A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84950405 | ||||||
| chr1:84950506
|
T | C | 13 | a0001c0001t0002g0233a0001c0001t0002g0308a0001c0001t0005g0038others(10): Show | 14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.747+1737A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84950506 | ||||||
| chr1:84950928
|
A | C | 29 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0076others(26): Show | 32 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.747+1315T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84950928 | ||||||
| chr1:84950931
|
A | G | 1 | a0010c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.747+1312T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84950931 | ||||||
| chr1:84951113
|
C | T | 65 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0064others(62): Show | 68 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.747+1130G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951113 | ||||||
| chr1:84951157
|
C | T | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0017g0100others(1): Show | 4 | HG00280.hp1 HG00735.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+1086G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951157 | ||||||
| chr1:84951158
|
G | A | 71 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0064others(68): Show | 73 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.747+1085C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951158 | ||||||
| chr1:84951166
|
G | A | 8 | a0003c0003t0001g0095a0003c0003t0005g0002a0003c0003t0005g0028others(5): Show | 9 | HG00642.hp2 HG01884.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.747+1077C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951166 | ||||||
| chr1:84951516
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.747+727T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951516 | ||||||
| chr1:84951695
|
T | C | 36 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0076others(33): Show | 37 | HG00639.hp2 HG01884.hp2 HG01981.hp1 others(34): Show |
intron_variant | MODIFIER | c.747+548A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951695 | ||||||
| chr1:84951844
|
A | G | 37 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0076others(34): Show | 38 | HG01884.hp2 HG01981.hp1 HG01993.hp1 others(35): Show |
intron_variant | MODIFIER | c.747+399T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951844 | ||||||
| chr1:84951845
|
G | A | 37 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0076others(34): Show | 38 | HG01884.hp2 HG01981.hp1 HG01993.hp1 others(35): Show |
intron_variant | MODIFIER | c.747+398C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951845 | ||||||
| chr1:84951863
|
A | T | 88 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0057others(85): Show | 90 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.747+380T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951863 | ||||||
| chr1:84951867
|
G | A | 1 | a0001c0001t0003g0185 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.747+376C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951867 | ||||||
| chr1:84951871
|
G | A | 3 | a0002c0002t0001g0122a0004c0004t0001g0045a0005c0005t0001g0044 | 3 | HG02615.hp2 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.747+372C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951871 | ||||||
| chr1:84951965
|
T | C | 2 | a0001c0001t0032g0246a0010c0010t0002g0245 | 2 | HG00642.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.747+278A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951965 | ||||||
| chr1:84952002
|
G | A | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.747+241C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84952002 | ||||||
| chr1:84952052
|
A | T | 1 | a0001c0001t0005g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.747+191T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84952052 | ||||||
| chr1:84952081
|
T | C | 42 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0076others(39): Show | 43 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(40): Show |
intron_variant | MODIFIER | c.747+162A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84952081 | ||||||
| chr1:84952096
|
G | A | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0057others(190): Show | 200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.747+147C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84952096 | ||||||
| chr1:84952136
|
A | C | 29 | a0001c0001t0002g0296a0001c0001t0005g0017a0001c0001t0005g0018others(26): Show | 30 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.747+107T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84952136 | ||||||
| chr1:84952624
|
C | G | 199 | a0001c0001t0001g0054a0001c0001t0001g0084a0001c0001t0002g0013others(196): Show | 208 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.566-94G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84952624 | ||||||
| chr1:84952658
|
G | C | 28 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(25): Show | 29 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.566-128C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84952658 | ||||||
| chr1:84952726
|
T | C | 1 | a0001c0001t0003g0213 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.566-196A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84952726 | ||||||
| chr1:84952962
|
A | G | 32 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(29): Show | 33 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.566-432T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84952962 | ||||||
| chr1:84953273
|
C | T | 27 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(24): Show | 28 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.566-743G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953273 | ||||||
| chr1:84953274
|
A | G | 33 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(30): Show | 34 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(31): Show |
intron_variant | MODIFIER | c.566-744T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953274 | ||||||
| chr1:84953376
|
G | A | 33 | a0001c0001t0002g0237a0001c0001t0002g0293a0001c0001t0002g0294others(30): Show | 35 | HG00597.hp1 HG01243.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.566-846C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953376 | ||||||
| chr1:84953407
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.566-877C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953407 | ||||||
| chr1:84953448
|
G | C | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.566-918C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953448 | ||||||
| chr1:84953529
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.566-999C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953529 | ||||||
| chr1:84953550
|
C | CA | 7 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0069others(4): Show | 7 | HG02055.hp2 HG02922.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-1021dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953550 | ||||||
| chr1:84953550
|
CA | C | 132 | a0001c0001t0001g0138a0001c0001t0002g0013a0001c0001t0002g0189others(129): Show | 139 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.566-1021delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953550 | ||||||
| chr1:84953550
|
CAAAA | C | 31 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(28): Show | 32 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.566-1024_566-1021d others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953550 | ||||||
| chr1:84953568
|
AT | A | 26 | a0001c0001t0002g0237a0001c0001t0002g0293a0001c0001t0002g0294others(23): Show | 27 | HG01243.hp2 HG02015.hp1 HG02132.hp2 others(24): Show |
intron_variant | MODIFIER | c.566-1039delA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953568 | ||||||
| chr1:84953569
|
T | A | 3 | a0001c0001t0001g0118a0001c0001t0007g0117a0001c0001t0021g0088 | 3 | HG01993.hp2 NA18974.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.566-1039A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953569 | ||||||
| chr1:84953592
|
T | A | 7 | a0001c0001t0002g0203a0001c0001t0002g0205a0001c0001t0003g0187others(4): Show | 7 | HG00639.hp1 HG01928.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-1062A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953592 | ||||||
| chr1:84953637
|
G | A | 23 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(20): Show | 24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.566-1107C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953637 | ||||||
| chr1:84953641
|
G | A | 3 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0006g0184 | 3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.566-1111C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953641 | ||||||
| chr1:84953668
|
T | C | 5 | a0002c0002t0001g0122a0004c0004t0001g0045a0005c0005t0001g0042others(2): Show | 5 | HG02615.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-1138A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953668 | ||||||
| chr1:84953694
|
T | C | 1 | a0001c0001t0007g0051 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.566-1164A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953694 | ||||||
| chr1:84953702
|
A | C | 64 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(61): Show | 67 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.566-1172T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953702 | ||||||
| chr1:84953705
|
A | G | 64 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(61): Show | 67 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.566-1175T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953705 | ||||||
| chr1:84953706
|
C | CTCA | 64 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(61): Show | 67 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.566-1177_566-1176i others(5): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953706 | ||||||
| chr1:84953708
|
G | T | 32 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(29): Show | 33 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.566-1178C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953708 | ||||||
| chr1:84953952
|
G | C | 1 | a0001c0001t0002g0199 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.566-1422C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953952 | ||||||
| chr1:84953993
|
A | G | 129 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(126): Show | 135 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.566-1463T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953993 | ||||||
| chr1:84954230
|
C | G | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.566-1700G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84954230 | ||||||
| chr1:84954264
|
T | C | 129 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(126): Show | 135 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.566-1734A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84954264 | ||||||
| chr1:84954361
|
A | C | 129 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(126): Show | 135 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.566-1831T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84954361 | ||||||
| chr1:84954665
|
G | A | 11 | a0001c0001t0002g0242a0001c0001t0002g0247a0001c0001t0003g0007others(8): Show | 14 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.565+1766C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84954665 | ||||||
| chr1:84954810
|
C | T | 129 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(126): Show | 135 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.565+1621G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84954810 | ||||||
| chr1:84955005
|
C | A | 1 | a0001c0001t0004g0136 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.565+1426G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955005 | ||||||
| chr1:84955094
|
C | T | 1 | a0001c0001t0003g0201 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.565+1337G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955094 | ||||||
| chr1:84955189
|
T | C | 9 | a0002c0002t0001g0122a0004c0004t0001g0039a0004c0004t0001g0040others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+1242A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955189 | ||||||
| chr1:84955305
|
C | T | 1 | a0001c0001t0010g0225 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.565+1126G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955305 | ||||||
| chr1:84955348
|
A | G | 1 | a0001c0001t0032g0246 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.565+1083T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955348 | ||||||
| chr1:84955359
|
G | A | 126 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(123): Show | 131 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.565+1072C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955359 | ||||||
| chr1:84955448
|
T | A | 129 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(126): Show | 135 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.565+983A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955448 | ||||||
| chr1:84955484
|
G | A | 129 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(126): Show | 135 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.565+947C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955484 | ||||||
| chr1:84955543
|
G | A | 3 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0006g0184 | 3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.565+888C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955543 | ||||||
| chr1:84955644
|
C | T | 55 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(52): Show | 56 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.565+787G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955644 | ||||||
| chr1:84955702
|
C | T | 1 | a0005c0005t0001g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.565+729G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955702 | ||||||
| chr1:84955954
|
A | G | 1 | a0001c0001t0002g0197 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.565+477T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955954 | ||||||
| chr1:84956112
|
T | C | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+319A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84956112 | ||||||
| chr1:84956154
|
G | GAA | 129 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(126): Show | 135 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.565+275_565+276dup others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84956154 | ||||||
| chr1:84956160
|
A | G | 3 | a0001c0001t0002g0296a0001c0001t0032g0246a0010c0010t0002g0245 | 3 | HG00642.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.565+271T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84956160 | ||||||
| chr1:84956215
|
C | T | 3 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0006g0184 | 3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.565+216G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84956215 | ||||||
| chr1:84956378
|
C | T | 197 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(194): Show | 206 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.565+53G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84956378 | ||||||
| chr1:84956695
|
T | C | 129 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(126): Show | 135 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.412-111A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84956695 | ||||||
| chr1:84956723
|
C | A | 1 | a0001c0001t0002g0308 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.412-139G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84956723 | ||||||
| chr1:84956869
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.412-285G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84956869 | ||||||
| chr1:84956951
|
C | T | 27 | a0001c0001t0002g0237a0001c0001t0002g0293a0001c0001t0002g0294others(24): Show | 28 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.412-367G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84956951 | ||||||
| chr1:84956979
|
G | T | 129 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(126): Show | 135 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.412-395C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84956979 | ||||||
| chr1:84957091
|
C | T | 3 | a0001c0001t0002g0296a0001c0001t0032g0246a0010c0010t0002g0245 | 3 | HG00642.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.412-507G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84957091 | ||||||
| chr1:84957125
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.412-541T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84957125 | ||||||
| chr1:84957537
|
T | C | 129 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(126): Show | 135 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.412-953A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84957537 | ||||||
| chr1:84957581
|
A | G | 129 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(126): Show | 135 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.411+948T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84957581 | ||||||
| chr1:84957792
|
G | T | 3 | a0001c0001t0001g0132a0006c0006t0001g0130a0006c0006t0025g0131 | 3 | HG01099.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.411+737C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84957792 | ||||||
| chr1:84957831
|
G | A | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.411+698C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84957831 | ||||||
| chr1:84957858
|
A | T | 129 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(126): Show | 135 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.411+671T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84957858 | ||||||
| chr1:84958037
|
T | C | 93 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(90): Show | 98 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.411+492A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84958037 | ||||||
| chr1:84958062
|
C | G | 23 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(20): Show | 24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.411+467G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84958062 | ||||||
| chr1:84958131
|
G | T | 1 | a0001c0001t0003g0280 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.411+398C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84958131 | ||||||
| chr1:84958198
|
C | T | 1 | a0001c0001t0003g0194 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.411+331G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84958198 | ||||||
| chr1:84958499
|
A | G | 128 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(125): Show | 134 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.411+30T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84958499 | ||||||
| chr1:84958796
|
A | G | 128 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(125): Show | 134 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.238-94T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84958796 | ||||||
| chr1:84958830
|
C | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0116a0001c0001t0001g0120others(1): Show | 4 | HG02630.hp2 HG02897.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-128G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84958830 | ||||||
| chr1:84958897
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.238-195G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84958897 | ||||||
| chr1:84958914
|
A | T | 128 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(125): Show | 134 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.238-212T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84958914 | ||||||
| chr1:84958977
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.238-275G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84958977 | ||||||
| chr1:84959012
|
T | G | 1 | a0001c0001t0003g0008 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.238-310A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959012 | ||||||
| chr1:84959187
|
A | T | 1 | a0001c0001t0003g0194 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.238-485T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959187 | ||||||
| chr1:84959255
|
A | G | 9 | a0002c0002t0001g0122a0004c0004t0001g0039a0004c0004t0001g0040others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.238-553T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959255 | ||||||
| chr1:84959404
|
G | A | 7 | a0001c0001t0002g0242a0001c0001t0003g0007a0001c0001t0003g0008others(4): Show | 9 | HG00140.hp1 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.238-702C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959404 | ||||||
| chr1:84959590
|
T | G | 1 | a0004c0004t0001g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.238-888A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959590 | ||||||
| chr1:84959591
|
C | A | 1 | a0004c0004t0001g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.238-889G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959591 | ||||||
| chr1:84959629
|
G | A | 23 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(20): Show | 24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.238-927C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959629 | ||||||
| chr1:84959646
|
A | C | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238-944T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959646 | ||||||
| chr1:84959746
|
C | A | 1 | a0001c0001t0003g0190 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.238-1044G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959746 | ||||||
| chr1:84959864
|
C | T | 1 | a0001c0001t0003g0185 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.238-1162G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959864 | ||||||
| chr1:84960023
|
A | G | 197 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(194): Show | 206 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.238-1321T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960023 | ||||||
| chr1:84960093
|
C | T | 6 | a0001c0001t0002g0257a0001c0001t0002g0285a0001c0001t0002g0291others(3): Show | 7 | HG01255.hp2 HG01358.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.238-1391G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960093 | ||||||
| chr1:84960106
|
G | T | 23 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(20): Show | 24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.238-1404C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960106 | ||||||
| chr1:84960138
|
T | C | 67 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(64): Show | 71 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.238-1436A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960138 | ||||||
| chr1:84960229
|
C | T | 23 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(20): Show | 24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.238-1527G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960229 | ||||||
| chr1:84960246
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0004g0091a0001c0001t0004g0092others(2): Show | 6 | HG00597.hp2 NA18964.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.238-1544C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960246 | ||||||
| chr1:84960391
|
T | C | 1 | a0001c0001t0002g0013 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.238-1689A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960391 | ||||||
| chr1:84960477
|
G | T | 121 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(118): Show | 126 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.238-1775C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960477 | ||||||
| chr1:84960573
|
T | C | 27 | a0001c0001t0002g0237a0001c0001t0002g0293a0001c0001t0002g0294others(24): Show | 28 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.238-1871A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960573 | ||||||
| chr1:84960689
|
G | A | 4 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0046others(1): Show | 4 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-1987C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960689 | ||||||
| chr1:84960701
|
G | A | 5 | a0002c0002t0001g0122a0004c0004t0001g0045a0005c0005t0001g0042others(2): Show | 5 | HG02615.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.238-1999C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960701 | ||||||
| chr1:84960739
|
A | C | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238-2037T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960739 | ||||||
| chr1:84960786
|
A | G | 1 | a0001c0001t0003g0214 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.238-2084T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960786 | ||||||
| chr1:84960791
|
T | C | 3 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0006g0184 | 3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.238-2089A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960791 | ||||||
| chr1:84960872
|
T | G | 124 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(121): Show | 130 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.238-2170A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960872 | ||||||
| chr1:84960879
|
C | T | 4 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0046others(1): Show | 4 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-2177G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960879 | ||||||
| chr1:84960888
|
G | GAAC | 124 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(121): Show | 130 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.238-2189_238-2187d others(5): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960888 | ||||||
| chr1:84960957
|
T | C | 1 | a0001c0001t0008g0227 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.238-2255A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960957 | ||||||
| chr1:84960981
|
C | A | 90 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(87): Show | 94 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.238-2279G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960981 | ||||||
| chr1:84961044
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.238-2342T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84961044 | ||||||
| chr1:84961124
|
G | A | 23 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(20): Show | 24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.238-2422C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84961124 | ||||||
| chr1:84961190
|
C | T | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238-2488G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84961190 | ||||||
| chr1:84961316
|
T | C | 4 | a0001c0001t0002g0192a0001c0001t0002g0296a0001c0001t0032g0246others(1): Show | 4 | HG00642.hp2 HG03130.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-2614A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84961316 | ||||||
| chr1:84961633
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.238-2931C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84961633 | ||||||
| chr1:84962009
|
C | T | 10 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0076others(7): Show | 10 | HG02055.hp1 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.238-3307G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84962009 | ||||||
| chr1:84962099
|
C | T | 4 | a0003c0003t0005g0028a0003c0003t0005g0029a0003c0003t0005g0030others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-3397G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84962099 | ||||||
| chr1:84962656
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.237+2893G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84962656 | ||||||
| chr1:84962705
|
C | T | 1 | a0001c0001t0002g0250 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.237+2844G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84962705 | ||||||
| chr1:84962708
|
G | C | 1 | a0001c0001t0001g0072 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.237+2841C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84962708 | ||||||
| chr1:84962721
|
A | G | 5 | a0002c0002t0001g0122a0004c0004t0001g0045a0005c0005t0001g0042others(2): Show | 5 | HG02615.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+2828T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84962721 | ||||||
| chr1:84962933
|
C | T | 1 | a0001c0001t0002g0303 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.237+2616G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84962933 | ||||||
| chr1:84963437
|
T | C | 27 | a0001c0001t0002g0237a0001c0001t0002g0293a0001c0001t0002g0294others(24): Show | 28 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.237+2112A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963437 | ||||||
| chr1:84963507
|
T | C | 1 | a0001c0001t0004g0146 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.237+2042A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963507 | ||||||
| chr1:84963588
|
T | C | 1 | a0001c0001t0003g0214 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.237+1961A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963588 | ||||||
| chr1:84963598
|
G | T | 1 | a0003c0003t0013g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.237+1951C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963598 | ||||||
| chr1:84963628
|
T | C | 1 | a0001c0001t0004g0156 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.237+1921A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963628 | ||||||
| chr1:84963761
|
A | G | 23 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(20): Show | 24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.237+1788T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963761 | ||||||
| chr1:84963804
|
T | C | 1 | a0001c0001t0002g0313 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.237+1745A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963804 | ||||||
| chr1:84963901
|
C | T | 125 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(122): Show | 130 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.237+1648G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963901 | ||||||
| chr1:84963912
|
T | C | 3 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0006g0184 | 3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.237+1637A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963912 | ||||||
| chr1:84964118
|
A | G | 72 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(69): Show | 76 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.237+1431T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964118 | ||||||
| chr1:84964207
|
C | T | 121 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(118): Show | 126 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.237+1342G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964207 | ||||||
| chr1:84964279
|
C | T | 1 | a0002c0002t0001g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.237+1270G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964279 | ||||||
| chr1:84964303
|
G | T | 5 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0016g0126others(2): Show | 5 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+1246C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964303 | ||||||
| chr1:84964526
|
T | TG | 122 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0113others(119): Show | 130 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.237+1022dupC | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964526 | ||||||
| chr1:84964527
|
G | T | 1 | a0001c0001t0002g0205 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.237+1022C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964527 | ||||||
| chr1:84964532
|
G | C | 8 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.237+1017C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964532 | ||||||
| chr1:84964533
|
G | GC | 3 | a0001c0001t0003g0012a0001c0001t0003g0259a0001c0001t0006g0287 | 4 | NA18970.hp1 NA18995.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+1015_237+1016i others(3): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964533 | ||||||
| chr1:84964681
|
A | C | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.237+868T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964681 | ||||||
| chr1:84964839
|
G | A | 125 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(122): Show | 130 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.237+710C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964839 | ||||||
| chr1:84964875
|
T | TA | 125 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(122): Show | 130 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.237+673dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964875 | ||||||
| chr1:84965027
|
A | G | 90 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(87): Show | 94 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.237+522T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84965027 | ||||||
| chr1:84965168
|
T | C | 125 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(122): Show | 130 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.237+381A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84965168 | ||||||
| chr1:84965192
|
T | C | 125 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(122): Show | 130 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.237+357A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84965192 | ||||||
| chr1:84965809
|
G | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0116a0001c0001t0001g0120others(1): Show | 4 | HG02630.hp2 HG02897.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.78-101C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84965809 | ||||||
| chr1:84966027
|
T | C | 125 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(122): Show | 130 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.78-319A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966027 | ||||||
| chr1:84966141
|
T | C | 125 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(122): Show | 130 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.78-433A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966141 | ||||||
| chr1:84966156
|
G | A | 125 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(122): Show | 130 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.78-448C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966156 | ||||||
| chr1:84966286
|
A | C | 1 | a0002c0002t0001g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.78-578T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966286 | ||||||
| chr1:84966716
|
C | A | 4 | a0001c0001t0002g0192a0001c0001t0002g0296a0001c0001t0032g0246others(1): Show | 4 | HG00642.hp2 HG03130.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-1008G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966716 | ||||||
| chr1:84966818
|
G | C | 1 | a0001c0001t0002g0296 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.78-1110C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966818 | ||||||
| chr1:84966822
|
A | G | 125 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(122): Show | 130 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.78-1114T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966822 | ||||||
| chr1:84966829
|
A | G | 1 | a0001c0001t0007g0115 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.78-1121T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966829 | ||||||
| chr1:84966834
|
A | C | 125 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(122): Show | 130 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.78-1126T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966834 | ||||||
| chr1:84966840
|
T | C | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.78-1132A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966840 | ||||||
| chr1:84966974
|
C | A | 3 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0006g0184 | 3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.78-1266G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966974 | ||||||
| chr1:84967120
|
T | C | 1 | a0001c0001t0009g0048 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.78-1412A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967120 | ||||||
| chr1:84967152
|
C | G | 4 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0069others(1): Show | 4 | HG02055.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-1444G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967152 | ||||||
| chr1:84967262
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.78-1554G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967262 | ||||||
| chr1:84967264
|
A | C | 67 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(64): Show | 71 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.78-1556T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967264 | ||||||
| chr1:84967580
|
A | G | 8 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.78-1872T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967580 | ||||||
| chr1:84967604
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.78-1896A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967604 | ||||||
| chr1:84967740
|
GGAGGGAG others(22): Show |
G | 21 | a0001c0001t0002g0293a0001c0001t0002g0298a0001c0001t0002g0300others(18): Show | 22 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.78-2061_78-2033del others(29): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967740 | ||||||
| chr1:84967748
|
G | A | 1 | a0001c0001t0006g0302 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.78-2040C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967748 | ||||||
| chr1:84967763
|
AAGG | A | 98 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(95): Show | 102 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.78-2058_78-2056del others(3): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967763 | ||||||
| chr1:84967782
|
G | A | 1 | a0001c0001t0006g0302 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.78-2074C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967782 | ||||||
| chr1:84967783
|
A | G | 1 | a0001c0001t0006g0302 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.78-2075T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967783 | ||||||
| chr1:84968393
|
G | C | 3 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0006g0184 | 3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.78-2685C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84968393 | ||||||
| chr1:84968417
|
T | C | 1 | a0001c0001t0009g0107 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.78-2709A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84968417 | ||||||
| chr1:84968423
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.78-2715T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84968423 | ||||||
| chr1:84968853
|
C | T | 93 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(90): Show | 97 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.78-3145G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84968853 | ||||||
| chr1:84968930
|
T | C | 197 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(194): Show | 206 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.78-3222A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84968930 | ||||||
| chr1:84969099
|
G | A | 11 | a0001c0001t0002g0242a0001c0001t0002g0247a0001c0001t0003g0007others(8): Show | 14 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.78-3391C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969099 | ||||||
| chr1:84969156
|
G | A | 2 | a0001c0001t0014g0015a0001c0001t0014g0020 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.78-3448C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969156 | ||||||
| chr1:84969326
|
T | G | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.78-3618A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969326 | ||||||
| chr1:84969362
|
G | A | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.78-3654C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969362 | ||||||
| chr1:84969487
|
T | C | 3 | a0001c0001t0002g0296a0001c0001t0032g0246a0010c0010t0002g0245 | 3 | HG00642.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.78-3779A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969487 | ||||||
| chr1:84969570
|
C | CA | 10 | a0001c0001t0001g0075a0001c0001t0001g0098a0001c0001t0001g0099others(7): Show | 10 | HG00735.hp1 HG01433.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.78-3863dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969570 | ||||||
| chr1:84969570
|
CA | C | 79 | a0001c0001t0002g0192a0001c0001t0002g0233a0001c0001t0002g0237others(76): Show | 84 | HG00140.hp1 HG00597.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.78-3863delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969570 | ||||||
| chr1:84969712
|
T | TA | 79 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(76): Show | 80 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.78-4005dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969712 | ||||||
| chr1:84969716
|
C | T | 3 | a0001c0001t0004g0127a0001c0001t0004g0128a0001c0001t0015g0125 | 3 | HG01081.hp1 HG01433.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.78-4008G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969716 | ||||||
| chr1:84969717
|
C | T | 23 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(20): Show | 24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.78-4009G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969717 | ||||||
| chr1:84969869
|
C | T | 125 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(122): Show | 130 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.78-4161G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969869 | ||||||
| chr1:84969877
|
G | A | 125 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(122): Show | 130 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.78-4169C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969877 | ||||||
| chr1:84969920
|
A | G | 3 | a0001c0001t0001g0118a0001c0001t0007g0117a0001c0001t0021g0088 | 3 | HG01993.hp2 NA18974.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.78-4212T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969920 | ||||||
| chr1:84969949
|
G | A | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.78-4241C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969949 | ||||||
| chr1:84969995
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.78-4287C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969995 | ||||||
| chr1:84970031
|
A | T | 3 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0006g0184 | 3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.78-4323T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970031 | ||||||
| chr1:84970043
|
A | G | 1 | a0001c0001t0002g0309 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.78-4335T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970043 | ||||||
| chr1:84970069
|
G | T | 125 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(122): Show | 130 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.78-4361C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970069 | ||||||
| chr1:84970204
|
G | T | 1 | a0001c0001t0002g0284 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.78-4496C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970204 | ||||||
| chr1:84970284
|
C | T | 1 | a0001c0001t0004g0148 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.78-4576G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970284 | ||||||
| chr1:84970292
|
C | T | 90 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(87): Show | 94 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.78-4584G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970292 | ||||||
| chr1:84970376
|
T | G | 1 | a0001c0001t0004g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.78-4668A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970376 | ||||||
| chr1:84970435
|
T | C | 129 | a0001c0001t0002g0192a0001c0001t0002g0197a0001c0001t0002g0198others(126): Show | 134 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.78-4727A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970435 | ||||||
| chr1:84970436
|
G | A | 1 | a0001c0001t0014g0019 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.78-4728C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970436 | ||||||
| chr1:84970445
|
G | A | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.78-4737C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970445 | ||||||
| chr1:84970515
|
CA | C | 10 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0002g0313others(7): Show | 10 | HG00558.hp1 HG01928.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.78-4808delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970515 | ||||||
| chr1:84970524
|
A | T | 2 | a0001c0001t0001g0118a0001c0001t0007g0117 | 2 | NA18974.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.78-4816T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970524 | ||||||
| chr1:84970528
|
A | T | 4 | a0001c0001t0001g0118a0001c0001t0003g0194a0001c0001t0007g0117others(1): Show | 4 | HG01993.hp2 HG02135.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.78-4820T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970528 | ||||||
| chr1:84970532
|
T | A | 1 | a0001c0001t0003g0201 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.78-4824A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970532 | ||||||
| chr1:84970613
|
G | T | 1 | a0001c0001t0002g0309 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.78-4905C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970613 | ||||||
| chr1:84970698
|
T | C | 1 | a0001c0001t0002g0296 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.78-4990A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970698 | ||||||
| chr1:84970707
|
G | C | 1 | a0001c0001t0004g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.78-4999C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970707 | ||||||
| chr1:84970715
|
T | C | 1 | a0001c0001t0002g0226 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.78-5007A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970715 | ||||||
| chr1:84970779
|
A | T | 197 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(194): Show | 206 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.78-5071T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970779 | ||||||
| chr1:84970945
|
G | A | 3 | a0001c0001t0002g0296a0001c0001t0032g0246a0010c0010t0002g0245 | 3 | HG00642.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.78-5237C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970945 | ||||||
| chr1:84971060
|
T | C | 1 | a0001c0001t0003g0252 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.78-5352A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971060 | ||||||
| chr1:84971243
|
G | A | 129 | a0001c0001t0002g0192a0001c0001t0002g0197a0001c0001t0002g0198others(126): Show | 134 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.78-5535C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971243 | ||||||
| chr1:84971254
|
T | C | 67 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(64): Show | 71 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.78-5546A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971254 | ||||||
| chr1:84971282
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.78-5574A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971282 | ||||||
| chr1:84971434
|
C | G | 9 | a0002c0002t0001g0122a0004c0004t0001g0039a0004c0004t0001g0040others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.78-5726G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971434 | ||||||
| chr1:84971499
|
T | TAC | 56 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(53): Show | 60 | HG00558.hp2 HG00621.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.78-5793_78-5792dup others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | ||||||
| chr1:84971499
|
T | TACAC | 5 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0007g0051others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.78-5795_78-5792dup others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | ||||||
| chr1:84971499
|
TAC | T | 66 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0066others(63): Show | 68 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.78-5793_78-5792del others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | ||||||
| chr1:84971499
|
TACAC | T | 57 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0078others(54): Show | 57 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.78-5795_78-5792del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | ||||||
| chr1:84971499
|
TACACAC | T | 66 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0193others(63): Show | 70 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.78-5797_78-5792del others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | ||||||
| chr1:84971499
|
TACACACA others(1): Show |
T | 15 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0177others(12): Show | 15 | HG00673.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.78-5799_78-5792del others(8): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | ||||||
| chr1:84971499
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0003g0186 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.78-5801_78-5792del others(10): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | ||||||
| chr1:84971499
|
TACACACA others(5): Show |
T | 5 | a0003c0003t0005g0002a0003c0003t0005g0028a0003c0003t0005g0029others(2): Show | 6 | HG01884.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.78-5803_78-5792del others(12): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | ||||||
| chr1:84971499
|
TACACACA others(9): Show |
T | 9 | a0002c0002t0001g0122a0004c0004t0001g0039a0004c0004t0001g0040others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.78-5807_78-5792del others(16): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | ||||||
| chr1:84971591
|
CAAAGT | C | 3 | a0001c0001t0002g0296a0001c0001t0032g0246a0010c0010t0002g0245 | 3 | HG00642.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.78-5888_78-5884del others(5): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971591 | ||||||
| chr1:84971605
|
A | G | 1 | a0001c0001t0007g0056 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.78-5897T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971605 | ||||||
| chr1:84971690
|
T | C | 3 | a0001c0001t0002g0296a0001c0001t0032g0246a0010c0010t0002g0245 | 3 | HG00642.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.78-5982A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971690 | ||||||
| chr1:84971803
|
C | T | 3 | a0001c0001t0002g0248a0001c0001t0003g0266a0001c0001t0003g0267 | 3 | NA18980.hp2 NA19057.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.78-6095G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971803 | ||||||
| chr1:84971804
|
G | A | 4 | a0001c0001t0002g0192a0001c0001t0002g0296a0001c0001t0032g0246others(1): Show | 4 | HG00642.hp2 HG03130.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-6096C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971804 | ||||||
| chr1:84972169
|
T | C | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.78-6461A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84972169 | ||||||
| chr1:84972204
|
C | A | 1 | a0001c0001t0002g0309 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.78-6496G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84972204 | ||||||
| chr1:84972349
|
T | C | 1 | a0001c0001t0005g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.78-6641A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84972349 | ||||||
| chr1:84972505
|
T | G | 2 | a0001c0001t0004g0129a0001c0001t0031g0087 | 2 | HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.78-6797A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84972505 | ||||||
| chr1:84972560
|
C | A | 120 | a0001c0001t0002g0192a0001c0001t0002g0197a0001c0001t0002g0198others(117): Show | 125 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.78-6852G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84972560 | ||||||
| chr1:84972636
|
G | A | 1 | a0001c0001t0011g0335 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.78-6928C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84972636 | ||||||
| chr1:84972726
|
T | C | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.78-7018A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84972726 | ||||||
| chr1:84972935
|
T | C | 1 | a0001c0001t0004g0155 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.78-7227A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84972935 | ||||||
| chr1:84973174
|
C | T | 3 | a0001c0001t0009g0048a0001c0001t0009g0049a0001c0001t0009g0050 | 3 | NA18747.hp1 NA18979.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.78-7466G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973174 | ||||||
| chr1:84973376
|
G | A | 190 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(187): Show | 199 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.78-7668C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973376 | ||||||
| chr1:84973464
|
G | A | 188 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(185): Show | 197 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.78-7756C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973464 | ||||||
| chr1:84973545
|
A | G | 23 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(20): Show | 24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.78-7837T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973545 | ||||||
| chr1:84973548
|
T | C | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.78-7840A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973548 | ||||||
| chr1:84973585
|
C | T | 67 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(64): Show | 71 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.78-7877G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973585 | ||||||
| chr1:84973621
|
T | G | 196 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(193): Show | 205 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.78-7913A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973621 | ||||||
| chr1:84973687
|
G | A | 5 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0078others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.78-7979C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973687 | ||||||
| chr1:84973771
|
T | C | 188 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(185): Show | 197 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.78-8063A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973771 | ||||||
| chr1:84973986
|
T | A | 188 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(185): Show | 197 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.78-8278A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973986 | ||||||
| chr1:84974021
|
C | A | 1 | a0001c0001t0001g0090 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.78-8313G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974021 | ||||||
| chr1:84974217
|
C | T | 8 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-8509G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974217 | ||||||
| chr1:84974313
|
C | A | 72 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(69): Show | 76 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.78-8605G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974313 | ||||||
| chr1:84974340
|
C | T | 67 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(64): Show | 71 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.78-8632G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974340 | ||||||
| chr1:84974341
|
C | G | 1 | a0001c0001t0002g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.78-8633G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974341 | ||||||
| chr1:84974451
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0007g0115 | 2 | NA18967.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.78-8743G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974451 | ||||||
| chr1:84974466
|
A | C | 1 | a0001c0001t0006g0231 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.78-8758T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974466 | ||||||
| chr1:84974530
|
C | T | 90 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(87): Show | 94 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.78-8822G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974530 | ||||||
| chr1:84974579
|
C | G | 1 | a0001c0001t0008g0211 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.78-8871G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974579 | ||||||
| chr1:84974633
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.78-8925C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974633 | ||||||
| chr1:84974665
|
G | T | 8 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-8957C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974665 | ||||||
| chr1:84974698
|
T | G | 1 | a0001c0001t0003g0324 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.78-8990A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974698 | ||||||
| chr1:84974708
|
G | C | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.78-9000C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974708 | ||||||
| chr1:84974964
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.78-9256C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974964 | ||||||
| chr1:84974965
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.78-9257T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974965 | ||||||
| chr1:84975017
|
G | A | 1 | a0001c0001t0004g0128 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.78-9309C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975017 | ||||||
| chr1:84975018
|
A | G | 3 | a0001c0001t0002g0296a0001c0001t0032g0246a0010c0010t0002g0245 | 3 | HG00642.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.78-9310T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975018 | ||||||
| chr1:84975110
|
G | A | 117 | a0001c0001t0002g0192a0001c0001t0002g0197a0001c0001t0002g0198others(114): Show | 122 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.78-9402C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975110 | ||||||
| chr1:84975110
|
G | T | 71 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(68): Show | 75 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.78-9402C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975110 | ||||||
| chr1:84975144
|
T | C | 1 | a0002c0002t0001g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.78-9436A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975144 | ||||||
| chr1:84975144
|
T | G | 1 | a0001c0001t0003g0208 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.78-9436A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975144 | ||||||
| chr1:84975154
|
C | T | 188 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(185): Show | 197 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.78-9446G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975154 | ||||||
| chr1:84975210
|
G | A | 1 | a0001c0001t0002g0309 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.78-9502C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975210 | ||||||
| chr1:84975234
|
C | G | 188 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(185): Show | 197 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.78-9526G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975234 | ||||||
| chr1:84975368
|
C | T | 196 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(193): Show | 205 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.78-9660G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975368 | ||||||
| chr1:84975521
|
A | C | 1 | a0001c0001t0002g0203 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.78-9813T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975521 | ||||||
| chr1:84975565
|
A | C | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.78-9857T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975565 | ||||||
| chr1:84975848
|
T | A | 1 | a0002c0002t0001g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.78-10140A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975848 | ||||||
| chr1:84975948
|
G | A | 3 | a0001c0001t0002g0308a0001c0001t0002g0319a0001c0001t0002g0320 | 3 | HG02145.hp2 HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.78-10240C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975948 | ||||||
| chr1:84976019
|
A | G | 90 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(87): Show | 94 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.78-10311T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976019 | ||||||
| chr1:84976102
|
C | T | 196 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(193): Show | 205 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.78-10394G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976102 | ||||||
| chr1:84976246
|
G | A | 196 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(193): Show | 205 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.78-10538C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976246 | ||||||
| chr1:84976263
|
G | T | 1 | a0001c0001t0006g0310 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.78-10555C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976263 | ||||||
| chr1:84976293
|
T | TA | 188 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(185): Show | 197 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.78-10586dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976293 | ||||||
| chr1:84976536
|
G | A | 71 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(68): Show | 75 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.78-10828C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976536 | ||||||
| chr1:84976553
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.78-10845C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976553 | ||||||
| chr1:84976564
|
G | A | 117 | a0001c0001t0002g0192a0001c0001t0002g0197a0001c0001t0002g0198others(114): Show | 122 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.78-10856C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976564 | ||||||
| chr1:84976697
|
T | C | 188 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(185): Show | 197 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.78-10989A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976697 | ||||||
| chr1:84976964
|
T | G | 196 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(193): Show | 205 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.78-11256A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976964 | ||||||
| chr1:84977025
|
A | G | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.78-11317T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977025 | ||||||
| chr1:84977123
|
A | G | 188 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(185): Show | 197 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.78-11415T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977123 | ||||||
| chr1:84977130
|
A | AT | 117 | a0001c0001t0002g0192a0001c0001t0002g0197a0001c0001t0002g0198others(114): Show | 122 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.78-11423dupA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977130 | ||||||
| chr1:84977130
|
A | T | 71 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(68): Show | 75 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.78-11422T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977130 | ||||||
| chr1:84977188
|
T | A | 1 | a0001c0001t0001g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.78-11480A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977188 | ||||||
| chr1:84977363
|
T | TAAC | 188 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(185): Show | 197 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.78-11656_78-11655i others(5): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977363 | ||||||
| chr1:84977440
|
T | C | 4 | a0001c0001t0002g0247a0002c0002t0002g0009a0002c0002t0002g0236others(1): Show | 5 | HG00639.hp2 HG01167.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-11732A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977440 | ||||||
| chr1:84977458
|
GA | G | 120 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0002g0192others(117): Show | 125 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.78-11751delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977458 | ||||||
| chr1:84977575
|
G | A | 17 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0021others(14): Show | 17 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.78-11867C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977575 | ||||||
| chr1:84977656
|
T | C | 10 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0068others(7): Show | 10 | HG01099.hp1 HG01109.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.78-11948A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977656 | ||||||
| chr1:84977737
|
G | T | 188 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(185): Show | 197 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.78-12029C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977737 | ||||||
| chr1:84977817
|
G | A | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.78-12109C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977817 | ||||||
| chr1:84977836
|
T | G | 188 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(185): Show | 197 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.78-12128A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977836 | ||||||
| chr1:84977849
|
C | T | 10 | a0001c0001t0002g0250a0001c0001t0002g0253a0001c0001t0002g0254others(7): Show | 10 | HG02071.hp1 HG02080.hp2 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.78-12141G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977849 | ||||||
| chr1:84977850
|
A | G | 71 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(68): Show | 75 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.78-12142T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977850 | ||||||
| chr1:84977922
|
A | G | 121 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0069others(118): Show | 126 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.78-12214T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977922 | ||||||
| chr1:84978124
|
C | T | 1 | a0001c0001t0017g0158 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.78-12416G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978124 | ||||||
| chr1:84978147
|
G | T | 188 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(185): Show | 197 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.78-12439C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978147 | ||||||
| chr1:84978276
|
CA | C | 179 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(176): Show | 188 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.78-12569delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978276 | ||||||
| chr1:84978334
|
AAAGC | A | 4 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0046others(1): Show | 4 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.78-12630_78-12627d others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978334 | ||||||
| chr1:84978404
|
T | A | 1 | a0003c0003t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.78-12696A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978404 | ||||||
| chr1:84978414
|
AAAAT | A | 188 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(185): Show | 197 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.78-12710_78-12707d others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978414 | ||||||
| chr1:84978542
|
C | T | 1 | a0001c0001t0013g0026 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.78-12834G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978542 | ||||||
| chr1:84978543
|
T | G | 70 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(67): Show | 74 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.78-12835A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978543 | ||||||
| chr1:84978562
|
A | C | 188 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(185): Show | 197 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.78-12854T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978562 | ||||||
| chr1:84978714
|
A | T | 1 | a0001c0001t0033g0282 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.78-13006T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978714 | ||||||
| chr1:84978718
|
T | A | 188 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(185): Show | 197 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.78-13010A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978718 | ||||||
| chr1:84978757
|
G | C | 8 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-13049C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978757 | ||||||
| chr1:84978799
|
A | T | 8 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-13091T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978799 | ||||||
| chr1:84978811
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.78-13103G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978811 | ||||||
| chr1:84978823
|
T | C | 7 | a0001c0001t0004g0079a0001c0001t0004g0129a0001c0001t0031g0087others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.78-13115A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978823 | ||||||
| chr1:84978926
|
C | G | 2 | a0001c0001t0001g0143a0001c0001t0023g0142 | 2 | NA18990.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.78-13218G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978926 | ||||||
| chr1:84979030
|
C | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 152 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.78-13322G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979030 | ||||||
| chr1:84979063
|
C | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 152 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.78-13355G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979063 | ||||||
| chr1:84979246
|
T | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 152 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.78-13538A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979246 | ||||||
| chr1:84979348
|
T | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 152 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.78-13640A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979348 | ||||||
| chr1:84979454
|
C | T | 3 | a0001c0001t0002g0248a0001c0001t0003g0266a0001c0001t0003g0267 | 3 | NA18980.hp2 NA19057.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.78-13746G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979454 | ||||||
| chr1:84979682
|
A | G | 8 | a0001c0001t0002g0250a0001c0001t0002g0269a0001c0001t0002g0270others(5): Show | 8 | HG02071.hp1 HG02080.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-13974T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979682 | ||||||
| chr1:84979701
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(144): Show | 153 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.78-13993A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979701 | ||||||
| chr1:84979717
|
C | A | 1 | a0001c0001t0002g0229 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.78-14009G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979717 | ||||||
| chr1:84979946
|
A | C | 1 | a0001c0001t0004g0156 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.78-14238T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979946 | ||||||
| chr1:84980001
|
C | T | 1 | a0001c0001t0003g0182 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.78-14293G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980001 | ||||||
| chr1:84980063
|
C | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 152 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.78-14355G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980063 | ||||||
| chr1:84980136
|
G | A | 1 | a0001c0001t0003g0259 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.78-14428C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980136 | ||||||
| chr1:84980143
|
G | A | 310 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(307): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.78-14435C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980143 | ||||||
| chr1:84980305
|
G | GA | 311 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(308): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.78-14598dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980305 | ||||||
| chr1:84980393
|
A | C | 3 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0006g0184 | 3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.78-14685T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980393 | ||||||
| chr1:84980439
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 144 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.78-14731G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980439 | ||||||
| chr1:84980580
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.78-14872C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980580 | ||||||
| chr1:84980803
|
G | A | 1 | a0003c0003t0005g0029 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.78-15095C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980803 | ||||||
| chr1:84981004
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.78-15296C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981004 | ||||||
| chr1:84981097
|
CAAT | C | 9 | a0001c0001t0001g0055a0001c0001t0001g0068a0001c0001t0001g0075others(6): Show | 9 | HG01099.hp1 HG01109.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.78-15392_78-15390d others(5): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981097 | ||||||
| chr1:84981651
|
G | A | 8 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+15145C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981651 | ||||||
| chr1:84981737
|
G | A | 3 | a0001c0001t0002g0296a0001c0001t0032g0246a0010c0010t0002g0245 | 3 | HG00642.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.77+15059C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981737 | ||||||
| chr1:84981740
|
C | T | 1 | a0001c0001t0003g0297 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.77+15056G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981740 | ||||||
| chr1:84981910
|
A | G | 44 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(41): Show | 44 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.77+14886T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981910 | ||||||
| chr1:84981951
|
CA | C | 169 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(166): Show | 177 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+14844delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981951 | ||||||
| chr1:84981976
|
A | T | 169 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(166): Show | 177 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+14820T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981976 | ||||||
| chr1:84981980
|
A | C | 168 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(165): Show | 176 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.77+14816T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981980 | ||||||
| chr1:84982074
|
G | GT | 157 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(154): Show | 165 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.77+14721dupA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982074 | ||||||
| chr1:84982074
|
G | GTT | 7 | a0001c0001t0002g0309a0001c0001t0010g0261a0004c0004t0001g0045others(4): Show | 7 | HG02615.hp2 HG02922.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+14720_77+14721d others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982074 | ||||||
| chr1:84982086
|
T | A | 1 | a0003c0003t0005g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.77+14710A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982086 | ||||||
| chr1:84982087
|
T | A | 5 | a0003c0003t0005g0002a0003c0003t0005g0028a0003c0003t0005g0029others(2): Show | 6 | HG01884.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+14709A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982087 | ||||||
| chr1:84982088
|
A | T | 174 | a0001c0001t0001g0067a0001c0001t0001g0116a0001c0001t0001g0120others(171): Show | 182 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.77+14708T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982088 | ||||||
| chr1:84982089
|
A | T | 77 | a0001c0001t0002g0013a0001c0001t0002g0191a0001c0001t0002g0192others(74): Show | 81 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.77+14707T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982089 | ||||||
| chr1:84982090
|
A | T | 13 | a0001c0001t0002g0253a0001c0001t0003g0190a0001c0001t0003g0281others(10): Show | 13 | HG00323.hp2 HG00558.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.77+14706T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982090 | ||||||
| chr1:84982146
|
T | C | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+14650A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982146 | ||||||
| chr1:84982156
|
A | G | 1 | a0001c0001t0003g0210 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.77+14640T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982156 | ||||||
| chr1:84982220
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0026g0085 | 2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.77+14576C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982220 | ||||||
| chr1:84982225
|
A | G | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+14571T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982225 | ||||||
| chr1:84982382
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0150a0001c0001t0007g0108 | 3 | HG01243.hp1 HG02148.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.77+14414G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982382 | ||||||
| chr1:84982383
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.77+14413C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982383 | ||||||
| chr1:84982445
|
T | A | 8 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+14351A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982445 | ||||||
| chr1:84982454
|
A | C | 1 | a0001c0001t0001g0106 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.77+14342T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982454 | ||||||
| chr1:84982579
|
G | A | 4 | a0001c0001t0002g0219a0001c0001t0002g0222a0001c0001t0012g0220others(1): Show | 4 | HG03654.hp1 HG03710.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+14217C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982579 | ||||||
| chr1:84982666
|
T | C | 169 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(166): Show | 177 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+14130A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982666 | ||||||
| chr1:84982668
|
A | G | 169 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(166): Show | 177 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+14128T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982668 | ||||||
| chr1:84982768
|
T | A | 7 | a0001c0001t0002g0309a0001c0001t0002g0313a0001c0001t0002g0322others(4): Show | 7 | HG04228.hp1 NA18951.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+14028A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982768 | ||||||
| chr1:84982778
|
C | T | 1 | a0001c0001t0005g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.77+14018G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982778 | ||||||
| chr1:84982901
|
A | G | 2 | a0001c0001t0003g0183a0001c0001t0006g0184 | 2 | NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.77+13895T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982901 | ||||||
| chr1:84982917
|
T | A | 2 | a0001c0001t0002g0250a0001c0001t0008g0273 | 2 | HG02071.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.77+13879A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982917 | ||||||
| chr1:84982983
|
G | A | 1 | a0001c0001t0002g0296 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.77+13813C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982983 | ||||||
| chr1:84983013
|
C | T | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+13783G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983013 | ||||||
| chr1:84983129
|
G | A | 9 | a0001c0001t0005g0024a0001c0001t0005g0027a0001c0001t0005g0032others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.77+13667C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983129 | ||||||
| chr1:84983228
|
C | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0116a0001c0001t0001g0120others(1): Show | 4 | HG02630.hp2 HG02897.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+13568G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983228 | ||||||
| chr1:84983264
|
TTTTTC | T | 169 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(166): Show | 177 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+13527_77+13531d others(7): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983264 | ||||||
| chr1:84983371
|
G | A | 3 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0006g0184 | 3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.77+13425C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983371 | ||||||
| chr1:84983397
|
T | C | 169 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(166): Show | 177 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+13399A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983397 | ||||||
| chr1:84983422
|
C | T | 28 | a0001c0001t0002g0237a0001c0001t0002g0293a0001c0001t0002g0294others(25): Show | 29 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.77+13374G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983422 | ||||||
| chr1:84983536
|
A | G | 169 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(166): Show | 177 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+13260T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983536 | ||||||
| chr1:84983568
|
T | C | 169 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(166): Show | 177 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+13228A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983568 | ||||||
| chr1:84983676
|
C | CT | 21 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0068others(18): Show | 21 | HG01099.hp1 HG01109.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.77+13119dupA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983676 | ||||||
| chr1:84983676
|
CT | C | 77 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(74): Show | 81 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.77+13119delA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983676 | ||||||
| chr1:84983802
|
G | A | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+12994C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983802 | ||||||
| chr1:84983822
|
G | A | 5 | a0001c0001t0001g0113a0001c0001t0004g0081a0001c0001t0004g0103others(2): Show | 5 | HG00408.hp1 HG00621.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+12974C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983822 | ||||||
| chr1:84983882
|
G | A | 3 | a0001c0001t0004g0127a0001c0001t0004g0128a0001c0001t0015g0125 | 3 | HG01081.hp1 HG01433.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.77+12914C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983882 | ||||||
| chr1:84983925
|
C | T | 1 | a0001c0001t0009g0107 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.77+12871G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983925 | ||||||
| chr1:84983966
|
G | C | 170 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(167): Show | 178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.77+12830C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983966 | ||||||
| chr1:84984014
|
T | C | 170 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(167): Show | 178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.77+12782A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984014 | ||||||
| chr1:84984040
|
T | C | 1 | a0001c0001t0018g0223 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.77+12756A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984040 | ||||||
| chr1:84984370
|
C | G | 4 | a0001c0001t0001g0154a0001c0001t0001g0174a0001c0001t0004g0155others(1): Show | 4 | HG00408.hp2 HG00621.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+12426G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984370 | ||||||
| chr1:84984386
|
G | T | 169 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(166): Show | 177 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+12410C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984386 | ||||||
| chr1:84984396
|
C | CT | 169 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(166): Show | 177 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+12399dupA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984396 | ||||||
| chr1:84984637
|
G | A | 169 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(166): Show | 177 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+12159C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984637 | ||||||
| chr1:84984681
|
A | G | 1 | a0001c0001t0002g0308 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.77+12115T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984681 | ||||||
| chr1:84984705
|
A | T | 1 | a0001c0001t0001g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.77+12091T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984705 | ||||||
| chr1:84984725
|
G | A | 2 | a0001c0001t0002g0013a0001c0001t0002g0276 | 3 | HG00280.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.77+12071C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984725 | ||||||
| chr1:84984789
|
G | A | 69 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(66): Show | 73 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.77+12007C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984789 | ||||||
| chr1:84984924
|
A | T | 1 | a0001c0001t0002g0260 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.77+11872T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984924 | ||||||
| chr1:84984944
|
T | C | 163 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(160): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.77+11852A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984944 | ||||||
| chr1:84984983
|
G | C | 8 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+11813C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984983 | ||||||
| chr1:84985043
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 147 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.77+11753G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985043 | ||||||
| chr1:84985237
|
T | C | 166 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(163): Show | 174 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.77+11559A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985237 | ||||||
| chr1:84985404
|
C | T | 166 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(163): Show | 174 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.77+11392G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985404 | ||||||
| chr1:84985460
|
G | A | 166 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(163): Show | 174 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.77+11336C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985460 | ||||||
| chr1:84985522
|
A | G | 1 | a0001c0001t0003g0316 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.77+11274T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985522 | ||||||
| chr1:84985571
|
G | T | 1 | a0004c0004t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.77+11225C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985571 | ||||||
| chr1:84985702
|
A | C | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+11094T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985702 | ||||||
| chr1:84985745
|
A | G | 1 | a0001c0001t0003g0186 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.77+11051T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985745 | ||||||
| chr1:84985942
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.77+10854A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985942 | ||||||
| chr1:84986082
|
T | C | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+10714A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986082 | ||||||
| chr1:84986159
|
C | T | 1 | a0001c0001t0002g0330 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.77+10637G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986159 | ||||||
| chr1:84986162
|
C | T | 3 | a0001c0001t0001g0132a0006c0006t0001g0130a0006c0006t0025g0131 | 3 | HG01099.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.77+10634G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986162 | ||||||
| chr1:84986163
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.77+10633C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986163 | ||||||
| chr1:84986241
|
T | C | 1 | a0001c0001t0002g0308 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.77+10555A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986241 | ||||||
| chr1:84986262
|
C | T | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+10534G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986262 | ||||||
| chr1:84986339
|
A | G | 311 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(308): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.77+10457T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986339 | ||||||
| chr1:84986404
|
G | C | 8 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+10392C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986404 | ||||||
| chr1:84986474
|
C | T | 1 | a0001c0001t0004g0181 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.77+10322G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986474 | ||||||
| chr1:84986475
|
G | A | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+10321C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986475 | ||||||
| chr1:84986543
|
C | CA | 79 | a0001c0001t0001g0173a0001c0001t0002g0013a0001c0001t0002g0189others(76): Show | 83 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.77+10252dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986543 | ||||||
| chr1:84986543
|
CA | C | 8 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0069others(5): Show | 8 | HG02055.hp2 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+10252delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986543 | ||||||
| chr1:84986592
|
G | GAATA | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+10200_77+10203d others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986592 | ||||||
| chr1:84986595
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.77+10201A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986595 | ||||||
| chr1:84986639
|
T | TGACAAAG others(65): Show |
1 | a0001c0001t0002g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.77+10085_77+10156d others(74): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986639 | ||||||
| chr1:84986711
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.77+10085C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986711 | ||||||
| chr1:84986769
|
C | T | 1 | a0001c0001t0002g0326 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.77+10027G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986769 | ||||||
| chr1:84986897
|
G | A | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9899C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986897 | ||||||
| chr1:84986967
|
A | T | 1 | a0003c0003t0013g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.77+9829T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986967 | ||||||
| chr1:84987025
|
G | A | 2 | a0001c0001t0003g0014a0001c0001t0003g0318 | 3 | NA18983.hp2 NA19000.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.77+9771C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987025 | ||||||
| chr1:84987054
|
T | C | 8 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+9742A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987054 | ||||||
| chr1:84987176
|
A | ATATC | 5 | a0001c0001t0001g0098a0001c0001t0002g0237a0001c0001t0003g0182others(2): Show | 5 | HG01433.hp2 HG02155.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+9616_77+9619dup others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987176 | ||||||
| chr1:84987176
|
ATATC | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 129 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.77+9616_77+9619del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987176 | ||||||
| chr1:84987176
|
ATATCTAT others(1): Show |
A | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0007g0056 | 3 | HG01099.hp1 HG02683.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.77+9612_77+9619del others(8): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987176 | ||||||
| chr1:84987184
|
C | G | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9612G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987184 | ||||||
| chr1:84987200
|
CTATCTAT others(7): Show |
C | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9582_77+9595del others(14): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987200 | ||||||
| chr1:84987206
|
A | T | 11 | a0001c0001t0002g0242a0001c0001t0002g0247a0001c0001t0003g0007others(8): Show | 14 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.77+9590T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987206 | ||||||
| chr1:84987208
|
C | A | 7 | a0001c0001t0001g0140a0001c0001t0001g0169a0001c0001t0004g0148others(4): Show | 8 | HG01928.hp1 HG01943.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+9588G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987208 | ||||||
| chr1:84987208
|
CTATA | C | 62 | a0001c0001t0002g0192a0001c0001t0002g0197a0001c0001t0002g0198others(59): Show | 65 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.77+9584_77+9587del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987208 | ||||||
| chr1:84987212
|
A | C | 29 | a0001c0001t0002g0237a0001c0001t0002g0293a0001c0001t0002g0294others(26): Show | 30 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.77+9584T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987212 | ||||||
| chr1:84987244
|
T | G | 70 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(67): Show | 74 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.77+9552A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987244 | ||||||
| chr1:84987245
|
G | A | 1 | a0001c0001t0035g0321 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.77+9551C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987245 | ||||||
| chr1:84987257
|
A | G | 1 | a0002c0002t0001g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.77+9539T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987257 | ||||||
| chr1:84987267
|
GTA | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.77+9527_77+9528del others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987267 | ||||||
| chr1:84987271
|
A | ATATATC | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9524_77+9525ins others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987271 | ||||||
| chr1:84987365
|
T | G | 9 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0076others(6): Show | 9 | HG02055.hp1 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+9431A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987365 | ||||||
| chr1:84987374
|
T | G | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9422A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987374 | ||||||
| chr1:84987386
|
A | G | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9410T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987386 | ||||||
| chr1:84987411
|
T | C | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9385A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987411 | ||||||
| chr1:84987413
|
T | C | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9383A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987413 | ||||||
| chr1:84987424
|
C | A | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9372G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987424 | ||||||
| chr1:84987432
|
G | GTATATAT others(65): Show |
8 | a0001c0001t0002g0250a0001c0001t0002g0269a0001c0001t0002g0270others(5): Show | 8 | HG02071.hp1 HG02080.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+9363_77+9364ins others(72): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987432 | ||||||
| chr1:84987439
|
G | C | 9 | a0001c0001t0002g0235a0001c0001t0002g0250a0001c0001t0002g0269others(6): Show | 9 | HG02071.hp1 HG02080.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.77+9357C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987439 | ||||||
| chr1:84987440
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.77+9356T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987440 | ||||||
| chr1:84987471
|
G | C | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.77+9325C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987471 | ||||||
| chr1:84987471
|
G | T | 45 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(42): Show | 46 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.77+9325C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987471 | ||||||
| chr1:84987472
|
A | C | 1 | a0001c0001t0008g0227 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.77+9324T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987472 | ||||||
| chr1:84987473
|
T | C | 45 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(42): Show | 46 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.77+9323A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987473 | ||||||
| chr1:84987474
|
A | ATATACAT others(193): Show |
1 | a0001c0001t0002g0235 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.77+9321_77+9322ins others(200): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987474 | ||||||
| chr1:84987488
|
A | G | 5 | a0001c0001t0002g0235a0004c0004t0001g0045a0005c0005t0001g0042others(2): Show | 5 | HG02615.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+9308T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987488 | ||||||
| chr1:84987489
|
C | CAT | 16 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0078others(13): Show | 16 | HG00609.hp2 HG00642.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.77+9305_77+9306dup others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | ||||||
| chr1:84987489
|
C | CATATATA others(161): Show |
13 | a0001c0001t0002g0257a0001c0001t0002g0285a0001c0001t0002g0291others(10): Show | 16 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.77+9306_77+9307ins others(168): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | ||||||
| chr1:84987489
|
C | CATATATA others(405): Show |
1 | a0004c0004t0001g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77+9306_77+9307ins others(412): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | ||||||
| chr1:84987489
|
C | CATATATA others(381): Show |
1 | a0007c0007t0004g0041 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+9306_77+9307ins others(388): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | ||||||
| chr1:84987489
|
C | CATATATA others(333): Show |
1 | a0004c0004t0001g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.77+9306_77+9307ins others(340): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | ||||||
| chr1:84987489
|
C | CATATATA others(123): Show |
1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+9306_77+9307ins others(130): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | ||||||
| chr1:84987489
|
C | CATATATG others(157): Show |
1 | a0001c0001t0002g0288 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.77+9306_77+9307ins others(164): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | ||||||
| chr1:84987489
|
C | CATATATG others(195): Show |
31 | a0001c0001t0002g0189a0001c0001t0002g0193a0001c0001t0002g0260others(28): Show | 31 | HG00323.hp2 HG00558.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.77+9306_77+9307ins others(202): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | ||||||
| chr1:84987489
|
C | CATATATG others(213): Show |
1 | a0001c0001t0006g0286 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.77+9306_77+9307ins others(220): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | ||||||
| chr1:84987489
|
C | CATATATG others(275): Show |
1 | a0001c0001t0002g0191 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.77+9306_77+9307ins others(282): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | ||||||
| chr1:84987489
|
C | CATATATG others(229): Show |
2 | a0001c0001t0002g0013a0001c0001t0002g0276 | 3 | HG00280.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.77+9306_77+9307ins others(236): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | ||||||
| chr1:84987489
|
C | CATATATG others(187): Show |
1 | a0001c0001t0002g0326 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.77+9306_77+9307ins others(194): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | ||||||
| chr1:84987489
|
C | CATATGTA others(37): Show |
20 | a0001c0001t0005g0018a0001c0001t0005g0021a0001c0001t0005g0024others(17): Show | 21 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.77+9306_77+9307ins others(44): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | ||||||
| chr1:84987489
|
C | T | 5 | a0001c0001t0002g0235a0004c0004t0001g0045a0005c0005t0001g0042others(2): Show | 5 | HG02615.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+9307G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | ||||||
| chr1:84987490
|
A | ATATGTAT others(49): Show |
4 | a0001c0001t0002g0228a0001c0001t0002g0320a0001c0001t0006g0234others(1): Show | 4 | HG02145.hp2 HG02155.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+9305_77+9306ins others(56): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987490 | ||||||
| chr1:84987490
|
A | ATATGTAT others(73): Show |
1 | a0001c0001t0002g0229 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.77+9305_77+9306ins others(80): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987490 | ||||||
| chr1:84987494
|
G | A | 65 | a0001c0001t0001g0059a0001c0001t0002g0013a0001c0001t0002g0189others(62): Show | 69 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.77+9302C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987494 | ||||||
| chr1:84987494
|
G | GTGTATAC others(3): Show |
1 | a0001c0001t0003g0202 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.77+9301_77+9302ins others(10): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987494 | ||||||
| chr1:84987495
|
T | TACATATA others(49): Show |
1 | a0004c0004t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.77+9300_77+9301ins others(56): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987495 | ||||||
| chr1:84987495
|
T | TAGATATA others(75): Show |
4 | a0004c0004t0001g0045a0005c0005t0001g0042a0005c0005t0001g0043others(1): Show | 4 | HG02615.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+9300_77+9301ins others(82): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987495 | ||||||
| chr1:84987495
|
T | TATATACC others(7): Show |
135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.77+9300_77+9301ins others(14): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987495 | ||||||
| chr1:84987495
|
T | TATATATC others(7): Show |
1 | a0001c0001t0007g0056 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.77+9300_77+9301ins others(14): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987495 | ||||||
| chr1:84987495
|
T | TGTATATA others(9): Show |
9 | a0001c0001t0001g0059a0001c0001t0002g0250a0001c0001t0002g0269others(6): Show | 9 | HG01346.hp1 HG02071.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+9300_77+9301ins others(16): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987495 | ||||||
| chr1:84987496
|
A | ATATACCT others(7): Show |
58 | a0001c0001t0001g0150a0001c0001t0002g0197a0001c0001t0002g0198others(55): Show | 60 | HG00609.hp1 HG00639.hp1 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.77+9299_77+9300ins others(14): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987496 | ||||||
| chr1:84987497
|
TAC | T | 28 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0069others(25): Show | 28 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.77+9297_77+9298del others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987497 | ||||||
| chr1:84987499
|
C | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.77+9297G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987499 | ||||||
| chr1:84987500
|
A | C | 1 | a0003c0003t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.77+9296T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987500 | ||||||
| chr1:84987503
|
G | C | 28 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0069others(25): Show | 28 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.77+9293C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987503 | ||||||
| chr1:84987503
|
G | T | 52 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0193others(49): Show | 56 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.77+9293C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987503 | ||||||
| chr1:84987504
|
A | ATATATAT others(177): Show |
1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+9291_77+9292ins others(184): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987504 | ||||||
| chr1:84987504
|
A | ATATATAT others(39): Show |
4 | a0001c0001t0001g0068a0001c0001t0001g0078a0001c0001t0001g0080others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+9291_77+9292ins others(46): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987504 | ||||||
| chr1:84987504
|
A | C | 28 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0069others(25): Show | 28 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.77+9292T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987504 | ||||||
| chr1:84987504
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.77+9292T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987504 | ||||||
| chr1:84987506
|
G | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(255): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.77+9290C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987506 | ||||||
| chr1:84987507
|
T | C | 1 | a0003c0003t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.77+9289A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987507 | ||||||
| chr1:84987509
|
T | TATACATA others(297): Show |
1 | a0001c0001t0002g0255 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.77+9286_77+9287ins others(304): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987509 | ||||||
| chr1:84987511
|
C | T | 62 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0193others(59): Show | 66 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.77+9285G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987511 | ||||||
| chr1:84987511
|
CATAT | C | 18 | a0001c0001t0002g0293a0001c0001t0002g0298a0001c0001t0002g0300others(15): Show | 18 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.77+9281_77+9284del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987511 | ||||||
| chr1:84987512
|
A | ACATATAT others(253): Show |
1 | a0001c0001t0003g0186 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.77+9283_77+9284ins others(260): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987512 | ||||||
| chr1:84987512
|
A | ATC | 5 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0320others(2): Show | 5 | HG00673.hp1 HG02145.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+9283_77+9284ins others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987512 | ||||||
| chr1:84987512
|
ATATG | A | 9 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0069others(6): Show | 9 | HG02055.hp2 HG02257.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+9280_77+9283del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987512 | ||||||
| chr1:84987513
|
T | C | 8 | a0001c0001t0002g0248a0001c0001t0002g0253a0001c0001t0002g0254others(5): Show | 8 | HG00609.hp2 HG00642.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+9283A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987513 | ||||||
| chr1:84987515
|
T | G | 1 | a0003c0003t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.77+9281A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987515 | ||||||
| chr1:84987515
|
TGTATATA others(43): Show |
T | 1 | a0008c0012t0005g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.77+9231_77+9280del others(50): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987515 | ||||||
| chr1:84987516
|
G | A | 63 | a0001c0001t0001g0075a0001c0001t0002g0013a0001c0001t0002g0189others(60): Show | 67 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.77+9280C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987516 | ||||||
| chr1:84987517
|
T | C | 27 | a0001c0001t0002g0189a0001c0001t0002g0193a0001c0001t0002g0257others(24): Show | 30 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.77+9279A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987517 | ||||||
| chr1:84987517
|
T | TAC | 25 | a0001c0001t0001g0075a0001c0001t0002g0013a0001c0001t0002g0235others(22): Show | 26 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.77+9278_77+9279ins others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987517 | ||||||
| chr1:84987517
|
T | TATAC | 5 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0320others(2): Show | 5 | HG00673.hp1 HG02145.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+9278_77+9279ins others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987517 | ||||||
| chr1:84987518
|
A | G | 2 | a0004c0004t0001g0040a0007c0007t0004g0041 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.77+9278T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987518 | ||||||
| chr1:84987521
|
T | C | 8 | a0001c0001t0002g0248a0001c0001t0002g0253a0001c0001t0002g0254others(5): Show | 8 | HG00609.hp2 HG00642.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+9275A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987521 | ||||||
| chr1:84987521
|
T | G | 6 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0320others(3): Show | 6 | HG00673.hp1 HG02145.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+9275A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987521 | ||||||
| chr1:84987521
|
T | TATGTATA others(17): Show |
59 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0078others(56): Show | 59 | HG00609.hp1 HG00639.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.77+9251_77+9274dup others(24): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987521 | ||||||
| chr1:84987523
|
T | C | 1 | a0003c0003t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.77+9273A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987523 | ||||||
| chr1:84987523
|
T | G | 27 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0069others(24): Show | 27 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.77+9273A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987523 | ||||||
| chr1:84987524
|
G | A | 15 | a0001c0001t0002g0191a0001c0001t0002g0248a0001c0001t0002g0253others(12): Show | 15 | HG00609.hp2 HG00642.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.77+9272C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987524 | ||||||
| chr1:84987526
|
ATACATCT others(3): Show |
A | 2 | a0001c0001t0005g0017a0001c0001t0005g0022 | 2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.77+9260_77+9269del others(10): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987526 | ||||||
| chr1:84987528
|
A | G | 1 | a0003c0003t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.77+9268T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987528 | ||||||
| chr1:84987529
|
C | T | 90 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0069others(87): Show | 94 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.77+9267G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987529 | ||||||
| chr1:84987531
|
T | C | 25 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0069others(22): Show | 25 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.77+9265A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987531 | ||||||
| chr1:84987531
|
T | G | 12 | a0001c0001t0002g0250a0001c0001t0002g0269a0001c0001t0002g0270others(9): Show | 12 | HG02071.hp1 HG02080.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.77+9265A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987531 | ||||||
| chr1:84987532
|
C | A | 54 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0069others(51): Show | 54 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.77+9264G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987532 | ||||||
| chr1:84987533
|
T | G | 51 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0193others(48): Show | 55 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.77+9263A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987533 | ||||||
| chr1:84987533
|
T | TATGTATA others(17): Show |
1 | a0001c0001t0002g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.77+9262_77+9263ins others(24): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987533 | ||||||
| chr1:84987536
|
G | A | 64 | a0001c0001t0001g0075a0001c0001t0002g0013a0001c0001t0002g0189others(61): Show | 68 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.77+9260C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987536 | ||||||
| chr1:84987536
|
GTATACAT others(41): Show |
G | 5 | a0001c0001t0001g0120a0001c0001t0002g0200a0001c0001t0002g0230others(2): Show | 5 | HG00642.hp1 HG01515.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+9212_77+9259del others(48): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987536 | ||||||
| chr1:84987537
|
T | C | 12 | a0001c0001t0002g0250a0001c0001t0002g0269a0001c0001t0002g0270others(9): Show | 12 | HG02071.hp1 HG02080.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.77+9259A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987537 | ||||||
| chr1:84987537
|
TATAC | T | 21 | a0001c0001t0002g0293a0001c0001t0002g0298a0001c0001t0002g0300others(18): Show | 21 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.77+9255_77+9258del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987537 | ||||||
| chr1:84987537
|
TATACATA others(33): Show |
T | 4 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0069others(1): Show | 4 | HG02055.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+9219_77+9258del others(40): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987537 | ||||||
| chr1:84987540
|
A | C | 1 | a0004c0004t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.77+9256T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987540 | ||||||
| chr1:84987541
|
C | CATATATA others(43): Show |
1 | a0001c0001t0001g0075 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.77+9254_77+9255ins others(50): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987541 | ||||||
| chr1:84987541
|
C | T | 15 | a0001c0001t0002g0191a0001c0001t0002g0248a0001c0001t0002g0253others(12): Show | 15 | HG00609.hp2 HG00642.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.77+9255G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987541 | ||||||
| chr1:84987544
|
A | C | 1 | a0001c0001t0002g0255 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.77+9252T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987544 | ||||||
| chr1:84987545
|
G | GATATATA others(3): Show |
2 | a0001c0001t0032g0246a0010c0010t0002g0245 | 2 | HG00642.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.77+9250_77+9251ins others(10): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987545 | ||||||
| chr1:84987545
|
G | T | 73 | a0001c0001t0001g0075a0001c0001t0002g0013a0001c0001t0002g0189others(70): Show | 77 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.77+9251C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987545 | ||||||
| chr1:84987548
|
G | A | 27 | a0001c0001t0002g0191a0001c0001t0002g0248a0001c0001t0002g0250others(24): Show | 27 | HG00609.hp2 HG00642.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.77+9248C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987548 | ||||||
| chr1:84987552
|
A | ATACATAT others(215): Show |
1 | a0001c0001t0002g0323 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.77+9243_77+9244ins others(222): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987552 | ||||||
| chr1:84987552
|
A | ATACATAT others(263): Show |
1 | a0001c0001t0002g0248 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.77+9243_77+9244ins others(270): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987552 | ||||||
| chr1:84987552
|
A | ATACATAT others(225): Show |
2 | a0001c0001t0003g0281a0001c0001t0012g0256 | 2 | HG02135.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.77+9243_77+9244ins others(232): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987552 | ||||||
| chr1:84987552
|
A | ATACATAT others(235): Show |
2 | a0001c0001t0002g0253a0001c0001t0002g0254 | 2 | NA19081.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.77+9243_77+9244ins others(242): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987552 | ||||||
| chr1:84987552
|
ACATC | A | 3 | a0001c0001t0003g0280a0001c0001t0005g0017a0001c0001t0005g0022 | 3 | HG01978.hp2 HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.77+9240_77+9243del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987552 | ||||||
| chr1:84987553
|
C | T | 56 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0193others(53): Show | 60 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.77+9243G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987553 | ||||||
| chr1:84987556
|
C | A | 27 | a0001c0001t0002g0191a0001c0001t0002g0248a0001c0001t0002g0250others(24): Show | 27 | HG00609.hp2 HG00642.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.77+9240G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987556 | ||||||
| chr1:84987557
|
T | G | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+9239A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987557 | ||||||
| chr1:84987560
|
G | A | 57 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0193others(54): Show | 61 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.77+9236C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987560 | ||||||
| chr1:84987560
|
G | GTATATAG others(3): Show |
3 | a0004c0004t0001g0040a0004c0004t0001g0046a0007c0007t0004g0041 | 3 | HG02109.hp2 HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.77+9235_77+9236ins others(10): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987560 | ||||||
| chr1:84987560
|
G | GTATATAT others(1): Show |
3 | a0001c0001t0002g0191a0001c0001t0002g0255a0001c0001t0003g0186 | 3 | HG01515.hp1 NA18975.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.77+9235_77+9236ins others(8): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987560 | ||||||
| chr1:84987560
|
G | GTATATAT others(173): Show |
1 | a0001c0001t0008g0274 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.77+9235_77+9236ins others(180): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987560 | ||||||
| chr1:84987560
|
G | GTATATAT others(173): Show |
7 | a0001c0001t0002g0250a0001c0001t0002g0269a0001c0001t0002g0270others(4): Show | 7 | HG02071.hp1 HG03669.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+9235_77+9236ins others(180): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987560 | ||||||
| chr1:84987560
|
GTATACAT others(17): Show |
G | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.77+9212_77+9235del others(24): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987560 | ||||||
| chr1:84987561
|
T | TATCTATA others(147): Show |
1 | a0004c0004t0001g0045 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.77+9234_77+9235ins others(154): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987561 | ||||||
| chr1:84987561
|
T | TATCTATA others(147): Show |
1 | a0005c0005t0001g0043 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.77+9234_77+9235ins others(154): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987561 | ||||||
| chr1:84987561
|
T | TATCTATA others(147): Show |
2 | a0005c0005t0001g0042a0005c0005t0001g0044 | 2 | HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.77+9234_77+9235ins others(154): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987561 | ||||||
| chr1:84987564
|
A | C | 1 | a0004c0004t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.77+9232T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987564 | ||||||
| chr1:84987565
|
C | T | 1 | a0004c0004t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.77+9231G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987565 | ||||||
| chr1:84987566
|
A | C | 2 | a0001c0001t0032g0246a0010c0010t0002g0245 | 2 | HG00642.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.77+9230T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987566 | ||||||
| chr1:84987569
|
G | T | 77 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(74): Show | 81 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.77+9227C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987569 | ||||||
| chr1:84987570
|
A | G | 1 | a0008c0012t0005g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.77+9226T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987570 | ||||||
| chr1:84987572
|
G | A | 4 | a0001c0001t0032g0246a0004c0004t0001g0039a0008c0012t0005g0016others(1): Show | 4 | HG00642.hp2 HG02145.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+9224C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987572 | ||||||
| chr1:84987573
|
T | C | 2 | a0001c0001t0032g0246a0010c0010t0002g0245 | 2 | HG00642.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.77+9223A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987573 | ||||||
| chr1:84987577
|
C | CATCTATG others(13): Show |
1 | a0001c0001t0004g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.77+9218_77+9219ins others(20): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987577 | ||||||
| chr1:84987577
|
C | T | 77 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(74): Show | 81 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.77+9219G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987577 | ||||||
| chr1:84987580
|
A | AGATATAT others(273): Show |
1 | a0010c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.77+9215_77+9216ins others(280): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987580 | ||||||
| chr1:84987580
|
A | AGATATAT others(251): Show |
1 | a0001c0001t0032g0246 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.77+9215_77+9216ins others(258): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987580 | ||||||
| chr1:84987580
|
A | ATATGTAT others(339): Show |
1 | a0004c0004t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.77+9215_77+9216ins others(346): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987580 | ||||||
| chr1:84987580
|
A | C | 129 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0067others(126): Show | 129 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(126): Show |
intron_variant | MODIFIER | c.77+9216T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987580 | ||||||
| chr1:84987581
|
G | C | 1 | a0001c0001t0004g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.77+9215C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987581 | ||||||
| chr1:84987581
|
G | T | 107 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(104): Show | 107 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.77+9215C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987581 | ||||||
| chr1:84987582
|
A | G | 2 | a0001c0001t0005g0017a0001c0001t0005g0022 | 2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.77+9214T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987582 | ||||||
| chr1:84987584
|
A | G | 107 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(104): Show | 107 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.77+9212T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987584 | ||||||
| chr1:84987585
|
T | G | 4 | a0004c0004t0001g0045a0005c0005t0001g0042a0005c0005t0001g0043others(1): Show | 4 | HG02615.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+9211A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987585 | ||||||
| chr1:84987589
|
C | CAT | 31 | a0001c0001t0002g0191a0001c0001t0002g0248a0001c0001t0002g0250others(28): Show | 31 | HG00609.hp2 HG01081.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.77+9205_77+9206dup others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | ||||||
| chr1:84987589
|
C | CATATATG others(61): Show |
3 | a0001c0001t0003g0010a0001c0001t0003g0251a0001c0001t0003g0252 | 4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+9206_77+9207ins others(68): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | ||||||
| chr1:84987589
|
C | CATATATG others(63): Show |
4 | a0001c0001t0002g0289a0001c0001t0003g0190a0001c0001t0006g0279others(1): Show | 4 | HG00323.hp2 NA18612.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+9206_77+9207ins others(70): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | ||||||
| chr1:84987589
|
C | CATATATG others(33): Show |
2 | a0001c0001t0002g0325a0001c0001t0002g0329 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.77+9206_77+9207ins others(40): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | ||||||
| chr1:84987589
|
C | CATATATG others(63): Show |
1 | a0001c0001t0002g0285 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.77+9206_77+9207ins others(70): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | ||||||
| chr1:84987589
|
C | CATATATG others(61): Show |
2 | a0001c0001t0002g0276a0001c0001t0013g0026 | 2 | HG00280.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.77+9206_77+9207ins others(68): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | ||||||
| chr1:84987589
|
C | CATATATG others(57): Show |
4 | a0001c0001t0002g0326a0001c0001t0002g0328a0001c0001t0002g0330others(1): Show | 4 | HG00741.hp2 HG01884.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+9206_77+9207ins others(64): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | ||||||
| chr1:84987589
|
C | CATATATG others(63): Show |
28 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0193others(25): Show | 31 | HG00558.hp1 HG01255.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.77+9206_77+9207ins others(70): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | ||||||
| chr1:84987589
|
C | T | 1 | a0008c0012t0005g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.77+9207G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | ||||||
| chr1:84987592
|
A | G | 1 | a0008c0012t0005g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.77+9204T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987592 | ||||||
| chr1:84987594
|
G | A | 1 | a0008c0012t0005g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.77+9202C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987594 | ||||||
| chr1:84987597
|
T | C | 1 | a0008c0012t0005g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.77+9199A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987597 | ||||||
| chr1:84987613
|
T | C | 1 | a0010c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.77+9183A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987613 | ||||||
| chr1:84987619
|
T | TATAC | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9173_77+9176dup others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987619 | ||||||
| chr1:84987619
|
T | TATACATA others(61): Show |
1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+9176_77+9177ins others(68): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987619 | ||||||
| chr1:84987631
|
T | C | 8 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+9165A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987631 | ||||||
| chr1:84987657
|
C | CATATGTA others(23): Show |
5 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0003g0010others(2): Show | 6 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+9138_77+9139ins others(30): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987657 | ||||||
| chr1:84987657
|
C | CATATGTA others(103): Show |
7 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+9138_77+9139ins others(110): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987657 | ||||||
| chr1:84987657
|
C | CATATGTA others(129): Show |
1 | a0007c0007t0004g0041 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+9138_77+9139ins others(136): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987657 | ||||||
| chr1:84987657
|
C | CGTATGTA others(41): Show |
1 | a0001c0001t0002g0191 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.77+9138_77+9139ins others(48): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987657 | ||||||
| chr1:84987659
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.77+9137A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987659 | ||||||
| chr1:84987659
|
T | TATGTATA others(41): Show |
55 | a0001c0001t0002g0189a0001c0001t0002g0193a0001c0001t0002g0235others(52): Show | 57 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.77+9136_77+9137ins others(48): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987659 | ||||||
| chr1:84987659
|
T | TATGTATA others(67): Show |
6 | a0001c0001t0002g0276a0001c0001t0006g0277a0001c0001t0006g0278others(3): Show | 6 | HG00280.hp2 HG02056.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+9136_77+9137ins others(74): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987659 | ||||||
| chr1:84987659
|
T | TATGTATA others(93): Show |
1 | a0010c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.77+9136_77+9137ins others(100): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987659 | ||||||
| chr1:84987659
|
T | TATGTATA others(119): Show |
1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+9136_77+9137ins others(126): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987659 | ||||||
| chr1:84987659
|
T | TATGTATA others(101): Show |
1 | a0001c0001t0002g0013 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.77+9136_77+9137ins others(108): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987659 | ||||||
| chr1:84987669
|
T | G | 13 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0003g0010others(10): Show | 14 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.77+9127A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987669 | ||||||
| chr1:84987670
|
G | A | 13 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0003g0010others(10): Show | 14 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.77+9126C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987670 | ||||||
| chr1:84987670
|
G | GTATATAG others(1): Show |
65 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(62): Show | 68 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.77+9118_77+9125dup others(8): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987670 | ||||||
| chr1:84987679
|
T | A | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+9117A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987679 | ||||||
| chr1:84987705
|
T | C | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9091A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987705 | ||||||
| chr1:84987730
|
T | C | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9066A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987730 | ||||||
| chr1:84987788
|
C | T | 88 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(85): Show | 92 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.77+9008G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987788 | ||||||
| chr1:84987903
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.77+8893A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987903 | ||||||
| chr1:84987978
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.77+8818A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987978 | ||||||
| chr1:84987996
|
T | C | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+8800A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987996 | ||||||
| chr1:84988132
|
G | A | 1 | a0001c0001t0009g0178 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.77+8664C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988132 | ||||||
| chr1:84988133
|
C | T | 1 | a0001c0001t0002g0250 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.77+8663G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988133 | ||||||
| chr1:84988182
|
A | G | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+8614T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988182 | ||||||
| chr1:84988210
|
T | A | 1 | a0001c0001t0002g0242 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.77+8586A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988210 | ||||||
| chr1:84988210
|
TA | T | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+8585delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988210 | ||||||
| chr1:84988211
|
A | T | 1 | a0001c0001t0001g0149 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.77+8585T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988211 | ||||||
| chr1:84988313
|
A | G | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+8483T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988313 | ||||||
| chr1:84988418
|
T | C | 3 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0006g0184 | 3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.77+8378A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988418 | ||||||
| chr1:84988426
|
C | G | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+8370G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988426 | ||||||
| chr1:84988442
|
G | A | 7 | a0001c0001t0002g0309a0001c0001t0002g0313a0001c0001t0002g0322others(4): Show | 7 | HG04228.hp1 NA18951.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+8354C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988442 | ||||||
| chr1:84988493
|
C | T | 3 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0006g0184 | 3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.77+8303G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988493 | ||||||
| chr1:84988495
|
C | G | 1 | a0003c0003t0005g0002 | 2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.77+8301G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988495 | ||||||
| chr1:84988545
|
C | A | 8 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+8251G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988545 | ||||||
| chr1:84988731
|
G | T | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.77+8065C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988731 | ||||||
| chr1:84988764
|
A | C | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+8032T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988764 | ||||||
| chr1:84988918
|
T | C | 7 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(4): Show | 7 | HG02257.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+7878A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988918 | ||||||
| chr1:84988918
|
T | G | 1 | a0004c0004t0001g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77+7878A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988918 | ||||||
| chr1:84988919
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.77+7877G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988919 | ||||||
| chr1:84988930
|
T | C | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+7866A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988930 | ||||||
| chr1:84989198
|
C | G | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+7598G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84989198 | ||||||
| chr1:84989325
|
T | C | 1 | a0001c0001t0009g0049 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.77+7471A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84989325 | ||||||
| chr1:84989679
|
A | C | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+7117T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84989679 | ||||||
| chr1:84989689
|
C | A | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+7107G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84989689 | ||||||
| chr1:84989690
|
A | T | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+7106T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84989690 | ||||||
| chr1:84989845
|
T | C | 3 | a0001c0001t0004g0091a0001c0001t0004g0092a0001c0001t0004g0094 | 3 | NA18966.hp2 NA18967.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.77+6951A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84989845 | ||||||
| chr1:84989849
|
C | T | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+6947G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84989849 | ||||||
| chr1:84989993
|
T | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 147 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.77+6803A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84989993 | ||||||
| chr1:84990019
|
G | A | 11 | a0001c0001t0002g0242a0001c0001t0002g0247a0001c0001t0003g0007others(8): Show | 14 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.77+6777C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990019 | ||||||
| chr1:84990024
|
T | C | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+6772A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990024 | ||||||
| chr1:84990140
|
C | CA | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+6655dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990140 | ||||||
| chr1:84990142
|
A | C | 88 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(85): Show | 92 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.77+6654T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990142 | ||||||
| chr1:84990213
|
G | T | 1 | a0001c0001t0004g0148 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.77+6583C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990213 | ||||||
| chr1:84990230
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.77+6566C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990230 | ||||||
| chr1:84990253
|
G | C | 78 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+6543C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990253 | ||||||
| chr1:84990297
|
C | CA | 32 | a0001c0001t0001g0057a0001c0001t0001g0070a0001c0001t0001g0080others(29): Show | 32 | HG00597.hp2 HG01099.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.77+6498dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990297 | ||||||
| chr1:84990297
|
CA | C | 82 | a0001c0001t0001g0082a0001c0001t0001g0106a0001c0001t0001g0175others(79): Show | 87 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.77+6498delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990297 | ||||||
| chr1:84990297
|
CAAA | C | 10 | a0001c0001t0002g0193a0001c0001t0002g0284a0001c0001t0002g0285others(7): Show | 10 | HG00558.hp1 HG00642.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.77+6496_77+6498del others(3): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990297 | ||||||
| chr1:84990297
|
CAAAA | C | 55 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0235others(52): Show | 59 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.77+6495_77+6498del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990297 | ||||||
| chr1:84990297
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0006g0295 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.77+6487_77+6498del others(12): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990297 | ||||||
| chr1:84990297
|
CAAAAAAA others(6): Show |
C | 12 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0003g0249others(9): Show | 12 | HG02015.hp1 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.77+6486_77+6498del others(13): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990297 | ||||||
| chr1:84990328
|
T | A | 2 | a0001c0001t0001g0114a0001c0001t0007g0115 | 2 | NA18967.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.77+6468A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990328 | ||||||
| chr1:84990436
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.77+6360A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990436 | ||||||
| chr1:84990446
|
T | TA | 77 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(74): Show | 81 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.77+6349dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990446 | ||||||
| chr1:84990447
|
A | T | 1 | a0001c0001t0002g0198 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.77+6349T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990447 | ||||||
| chr1:84990508
|
T | C | 3 | a0001c0001t0001g0118a0001c0001t0007g0117a0001c0001t0021g0088 | 3 | HG01993.hp2 NA18974.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.77+6288A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990508 | ||||||
| chr1:84990523
|
C | T | 7 | a0001c0001t0013g0026a0003c0003t0005g0002a0003c0003t0005g0028others(4): Show | 8 | HG01884.hp2 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+6273G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990523 | ||||||
| chr1:84990641
|
G | C | 4 | a0004c0004t0001g0045a0005c0005t0001g0042a0005c0005t0001g0043others(1): Show | 4 | HG02615.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+6155C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990641 | ||||||
| chr1:84990813
|
A | T | 1 | a0001c0001t0002g0197 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.77+5983T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990813 | ||||||
| chr1:84990826
|
TG | T | 67 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(64): Show | 71 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.77+5969delC | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990826 | ||||||
| chr1:84990906
|
G | A | 8 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+5890C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990906 | ||||||
| chr1:84990942
|
A | G | 5 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0003g0249others(2): Show | 5 | HG02015.hp1 NA18961.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+5854T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990942 | ||||||
| chr1:84991096
|
G | C | 1 | a0001c0001t0001g0174 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.77+5700C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84991096 | ||||||
| chr1:84991219
|
T | C | 68 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(65): Show | 72 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.77+5577A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84991219 | ||||||
| chr1:84991278
|
T | G | 68 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(65): Show | 72 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.77+5518A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84991278 | ||||||
| chr1:84991383
|
C | T | 301 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.77+5413G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84991383 | ||||||
| chr1:84991400
|
C | T | 1 | a0001c0001t0027g0147 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.77+5396G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84991400 | ||||||
| chr1:84991604
|
A | G | 1 | a0001c0001t0005g0027 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.77+5192T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84991604 | ||||||
| chr1:84991678
|
T | C | 309 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(306): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.77+5118A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84991678 | ||||||
| chr1:84992248
|
C | G | 1 | a0010c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.77+4548G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992248 | ||||||
| chr1:84992250
|
C | G | 162 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(159): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.77+4546G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992250 | ||||||
| chr1:84992372
|
C | T | 5 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0004g0146others(2): Show | 5 | HG00558.hp2 NA18960.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+4424G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992372 | ||||||
| chr1:84992374
|
C | T | 8 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+4422G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992374 | ||||||
| chr1:84992400
|
A | T | 8 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+4396T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992400 | ||||||
| chr1:84992402
|
A | G | 2 | a0001c0001t0032g0246a0010c0010t0002g0245 | 2 | HG00642.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.77+4394T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992402 | ||||||
| chr1:84992435
|
A | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(95): Show | 104 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.77+4361T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992435 | ||||||
| chr1:84992465
|
C | T | 162 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(159): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.77+4331G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992465 | ||||||
| chr1:84992752
|
T | TA | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.77+4043dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992752 | ||||||
| chr1:84992759
|
A | AC | 77 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(74): Show | 78 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.77+4036dupG | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992759 | ||||||
| chr1:84992879
|
T | TC | 162 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(159): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.77+3916dupG | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992879 | ||||||
| chr1:84993063
|
C | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.77+3733G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993063 | ||||||
| chr1:84993179
|
G | T | 162 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(159): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.77+3617C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993179 | ||||||
| chr1:84993309
|
G | A | 1 | a0004c0004t0001g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77+3487C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993309 | ||||||
| chr1:84993325
|
T | C | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+3471A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993325 | ||||||
| chr1:84993380
|
T | G | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+3416A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993380 | ||||||
| chr1:84993505
|
T | C | 162 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(159): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.77+3291A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993505 | ||||||
| chr1:84993506
|
G | A | 1 | a0001c0001t0003g0290 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.77+3290C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993506 | ||||||
| chr1:84993515
|
G | A | 161 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(158): Show | 169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+3281C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993515 | ||||||
| chr1:84993575
|
G | T | 162 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(159): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.77+3221C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993575 | ||||||
| chr1:84993616
|
T | TAA | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(152): Show | 162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.77+3179_77+3180ins others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993616 | ||||||
| chr1:84993616
|
T | TAG | 161 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(158): Show | 169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+3179_77+3180ins others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993616 | ||||||
| chr1:84993617
|
G | A | 1 | a0001c0001t0006g0196 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.77+3179C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993617 | ||||||
| chr1:84993618
|
T | G | 1 | a0001c0001t0006g0196 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.77+3178A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993618 | ||||||
| chr1:84993619
|
C | CT | 16 | a0001c0001t0001g0059a0001c0001t0001g0072a0001c0001t0001g0123others(13): Show | 16 | HG01106.hp2 HG01346.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.77+3176dupA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993619 | ||||||
| chr1:84993619
|
C | G | 1 | a0001c0001t0006g0196 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.77+3177G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993619 | ||||||
| chr1:84993619
|
CTTT | C | 166 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(163): Show | 174 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.77+3174_77+3176del others(3): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993619 | ||||||
| chr1:84993621
|
T | C | 1 | a0001c0001t0006g0196 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.77+3175A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993621 | ||||||
| chr1:84993672
|
G | A | 1 | a0001c0001t0006g0234 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.77+3124C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993672 | ||||||
| chr1:84993716
|
C | T | 3 | a0001c0001t0004g0047a0001c0001t0004g0097a0001c0001t0004g0181 | 3 | HG00735.hp2 HG01074.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.77+3080G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993716 | ||||||
| chr1:84993742
|
T | C | 1 | a0002c0002t0001g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.77+3054A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993742 | ||||||
| chr1:84993786
|
A | G | 310 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(307): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.77+3010T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993786 | ||||||
| chr1:84993791
|
C | T | 8 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+3005G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993791 | ||||||
| chr1:84993792
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.77+3004C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993792 | ||||||
| chr1:84993868
|
G | A | 1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+2928C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993868 | ||||||
| chr1:84993882
|
G | A | 6 | a0001c0001t0032g0246a0004c0004t0001g0039a0004c0004t0001g0040others(3): Show | 6 | HG00642.hp2 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+2914C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993882 | ||||||
| chr1:84993893
|
G | A | 8 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+2903C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993893 | ||||||
| chr1:84994047
|
C | T | 162 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(159): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.77+2749G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994047 | ||||||
| chr1:84994048
|
A | G | 162 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(159): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.77+2748T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994048 | ||||||
| chr1:84994065
|
T | C | 2 | a0001c0001t0032g0246a0010c0010t0002g0245 | 2 | HG00642.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.77+2731A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994065 | ||||||
| chr1:84994086
|
A | G | 8 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0045others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+2710T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994086 | ||||||
| chr1:84994338
|
T | C | 67 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(64): Show | 71 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.77+2458A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994338 | ||||||
| chr1:84994354
|
CCTCT | C | 162 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(159): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.77+2438_77+2441del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994354 | ||||||
| chr1:84994390
|
C | T | 1 | a0001c0001t0007g0096 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.77+2406G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994390 | ||||||
| chr1:84994442
|
CCTTCATC others(6): Show |
C | 1 | a0001c0001t0002g0291 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.77+2341_77+2353del others(13): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994442 | ||||||
| chr1:84994464
|
C | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(305): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.77+2332G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994464 | ||||||
| chr1:84994820
|
C | T | 1 | a0001c0001t0009g0048 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.77+1976G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994820 | ||||||
| chr1:84994876
|
C | A | 5 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0009g0178others(2): Show | 5 | HG00673.hp2 NA18968.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+1920G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994876 | ||||||
| chr1:84995203
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.77+1593T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995203 | ||||||
| chr1:84995229
|
C | A | 170 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(167): Show | 178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.77+1567G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995229 | ||||||
| chr1:84995239
|
T | C | 162 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(159): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.77+1557A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995239 | ||||||
| chr1:84995248
|
A | G | 8 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0076others(5): Show | 8 | HG02055.hp1 HG02486.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+1548T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995248 | ||||||
| chr1:84995262
|
CT | C | 162 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(159): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.77+1533delA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995262 | ||||||
| chr1:84995283
|
T | C | 1 | a0001c0001t0001g0006 | 2 | NA18964.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.77+1513A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995283 | ||||||
| chr1:84995347
|
A | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 146 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.77+1449T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995347 | ||||||
| chr1:84995469
|
G | C | 1 | a0001c0001t0002g0247 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.77+1327C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995469 | ||||||
| chr1:84995573
|
C | T | 162 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(159): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.77+1223G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995573 | ||||||
| chr1:84995586
|
AG | A | 162 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(159): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.77+1209delC | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995586 | ||||||
| chr1:84995724
|
C | T | 162 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(159): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.77+1072G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995724 | ||||||
| chr1:84995804
|
T | A | 2 | a0001c0001t0003g0194a0001c0001t0003g0195 | 2 | HG02135.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.77+992A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995804 | ||||||
| chr1:84995804
|
T | TA | 3 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0006g0184 | 3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.77+991_77+992insT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995804 | ||||||
| chr1:84995804
|
T | TAA | 15 | a0001c0001t0002g0237a0001c0001t0002g0242a0001c0001t0002g0247others(12): Show | 18 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.77+991_77+992insTT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995804 | ||||||
| chr1:84995804
|
T | TAAA | 33 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0296others(30): Show | 34 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(31): Show |
intron_variant | MODIFIER | c.77+991_77+992insTT others(1): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995804 | ||||||
| chr1:84995804
|
T | TAAAA | 9 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0001t0002g0325others(6): Show | 9 | HG00609.hp2 HG00741.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.77+991_77+992insTT others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995804 | ||||||
| chr1:84995805
|
T | A | 62 | a0001c0001t0002g0237a0001c0001t0002g0242a0001c0001t0002g0247others(59): Show | 66 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.77+991A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995805 | ||||||
| chr1:84995805
|
T | TAAA | 42 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199others(39): Show | 42 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.77+990_77+991insTT others(1): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995805 | ||||||
| chr1:84995805
|
T | TAAAA | 53 | a0001c0001t0002g0013a0001c0001t0002g0248a0001c0001t0002g0250others(50): Show | 57 | HG00280.hp2 HG00558.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.77+990_77+991insTT others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995805 | ||||||
| chr1:84995806
|
T | A | 159 | a0001c0001t0002g0013a0001c0001t0002g0192a0001c0001t0002g0193others(156): Show | 167 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.77+990A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995806 | ||||||
| chr1:84995807
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.77+989T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995807 | ||||||
| chr1:84995869
|
T | A | 4 | a0004c0004t0001g0039a0004c0004t0001g0040a0004c0004t0001g0046others(1): Show | 4 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+927A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995869 | ||||||
| chr1:84995981
|
A | G | 2 | a0001c0001t0003g0187a0001c0001t0003g0188 | 2 | HG02040.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.77+815T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995981 | ||||||
| chr1:84996030
|
A | C | 1 | a0001c0001t0003g0186 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.77+766T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996030 | ||||||
| chr1:84996113
|
A | G | 1 | a0001c0001t0005g0032 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.77+683T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996113 | ||||||
| chr1:84996179
|
A | C | 1 | a0001c0001t0003g0185 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.77+617T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996179 | ||||||
| chr1:84996263
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.77+533T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996263 | ||||||
| chr1:84996292
|
T | C | 6 | a0001c0001t0002g0325a0001c0001t0002g0326a0001c0001t0002g0328others(3): Show | 6 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+504A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996292 | ||||||
| chr1:84996393
|
C | CAT | 10 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0093others(7): Show | 10 | HG00323.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.77+401_77+402dupAT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
C | CATAT | 8 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0004g0081others(5): Show | 8 | HG01993.hp2 HG02280.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.77+399_77+402dupAT others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
C | CATATAT | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG02258.hp2 HG02486.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+397_77+402dupAT others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
C | CATATATA others(1): Show |
5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0074others(2): Show | 5 | HG02109.hp1 HG02809.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+395_77+402dupAT others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
C | CATATATA others(3): Show |
5 | a0001c0001t0001g0003a0001c0001t0001g0068a0001c0001t0001g0069others(2): Show | 6 | HG01109.hp2 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+393_77+402dupAT others(8): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
C | CATATATA others(5): Show |
6 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0066others(3): Show | 6 | HG01106.hp2 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+391_77+402dupAT others(10): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
C | CATATATA others(7): Show |
6 | a0001c0001t0001g0059a0001c0001t0004g0047a0001c0001t0007g0060others(3): Show | 6 | HG00735.hp2 HG01346.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+389_77+402dupAT others(12): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
C | CATATATA others(9): Show |
5 | a0001c0001t0001g0057a0001c0001t0007g0056a0002c0002t0001g0058others(2): Show | 5 | HG02683.hp2 HG02922.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+387_77+402dupAT others(14): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
C | CATATATA others(11): Show |
2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG01099.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.77+385_77+402dupAT others(16): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
C | CATATATA others(13): Show |
4 | a0001c0001t0001g0053a0002c0002t0001g0052a0004c0004t0001g0040others(1): Show | 4 | HG02572.hp2 HG02896.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+383_77+402dupAT others(18): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
C | CATATATA others(15): Show |
2 | a0001c0001t0007g0051a0004c0004t0001g0039 | 2 | HG02257.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.77+381_77+402dupAT others(20): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
CAT | C | 17 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0109others(14): Show | 18 | HG00621.hp2 HG01070.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.77+401_77+402delAT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
CATAT | C | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG02886.hp2 HG02897.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+399_77+402delAT others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
CATATAT | C | 8 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0005g0027others(5): Show | 9 | HG01884.hp2 HG02055.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+397_77+402delAT others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
CATATATA others(3): Show |
C | 11 | a0001c0001t0004g0127a0001c0001t0004g0128a0001c0001t0004g0129others(8): Show | 11 | HG00140.hp2 HG01081.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.77+393_77+402delAT others(8): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
CATATATA others(5): Show |
C | 1 | a0001c0001t0005g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.77+391_77+402delAT others(10): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
CATATATA others(7): Show |
C | 1 | a0006c0006t0001g0130 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.77+389_77+402delAT others(12): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
CATATATA others(11): Show |
C | 3 | a0001c0001t0001g0132a0001c0001t0029g0133a0006c0006t0025g0131 | 3 | HG01099.hp2 HG03209.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.77+385_77+402delAT others(16): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
CATATATA others(13): Show |
C | 51 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0134others(48): Show | 55 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.77+383_77+402delAT others(18): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
CATATATA others(17): Show |
C | 4 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0004g0179others(1): Show | 4 | HG02155.hp1 HG03453.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+379_77+402delAT others(22): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996393
|
CATATATA others(19): Show |
C | 159 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(156): Show | 167 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.77+377_77+402delAT others(24): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | ||||||
| chr1:84996429
|
T | TATATATA others(4): Show |
1 | a0011c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+366_77+367insTA others(9): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996429 | ||||||
| chr1:84996449
|
C | T | 3 | a0001c0001t0009g0048a0001c0001t0009g0049a0001c0001t0009g0050 | 3 | NA18747.hp1 NA18979.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.77+347G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996449 | ||||||
| chr1:84996511
|
G | C | 162 | a0001c0001t0002g0013a0001c0001t0002g0189a0001c0001t0002g0191others(159): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.77+285C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996511 | ||||||
| chr1:84996520
|
C | T | 1 | a0001c0001t0004g0047 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.77+276G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996520 | ||||||
| chr1:84996563
|
G | A | 1 | a0001c0001t0004g0181 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.77+233C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996563 | ||||||
| chr1:84996619
|
A | T | 1 | a0001c0001t0014g0015 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.77+177T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996619 |