| geneid | 4124 |
|---|---|
| ensemblid | ENSG00000112893.10 |
| hgncid | 6824 |
| symbol | MAN2A1 |
| name | mannosidase alpha class 2A member 1 |
| refseq_nuc | NM_002372.4 |
| refseq_prot | NP_002363.2 |
| ensembl_nuc | ENST00000261483.5 |
| ensembl_prot | ENSP00000261483.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 109689927 |
| end | 109869625 |
| strand | + |
| ver | v1.2 |
| region | chr5:109689927-109869625 |
| region5000 | chr5:109684927-109874625 |
| regionname0 | MAN2A1_chr5_109689927_109869625 |
| regionname5000 | MAN2A1_chr5_109684927_109874625 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1144 | 198 | 61 | 56 | 48 | 12 | 19 | 38 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0002 | 0/0 | 1143 | 79 | 4 | 15 | 44 | 2 | 14 | 32 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0003 | 0/0 | 1144 | 8 | 0 | 0 | 8 | 0 | 0 | 4 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0004 | 0/0 | 1144 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0005 | 0/0 | 1144 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0006 | 0/0 | 1144 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0007 | 0/0 | 1143 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0008 | 0/0 | 1143 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0009 | 0/0 | 1144 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0010 | 0/0 | 1144 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3435 | 78 | 27 | 22 | 22 | 4 | 2 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0002 | 0/0 | 3432 | 78 | 4 | 14 | 44 | 2 | 14 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0003 | 1/0 | 3435 | 60 | 2 | 22 | 18 | 5 | 12 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0004 | 0/0 | 3435 | 27 | 15 | 8 | 0 | 1 | 3 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0005 | 0/0 | 3435 | 15 | 2 | 4 | 6 | 2 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0006 | 0/0 | 3435 | 10 | 10 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0007 | 0/0 | 3435 | 8 | 0 | 0 | 8 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0008 | 0/0 | 3435 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0009 | 0/0 | 3435 | 3 | 1 | 0 | 2 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0010 | 0/0 | 3435 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0011 | 0/0 | 3435 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0012 | 0/0 | 3435 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0013 | 0/0 | 3435 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0014 | 0/0 | 3432 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0015 | 0/0 | 3435 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0016 | 0/0 | 3435 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0017 | 0/0 | 3432 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0018 | 0/0 | 3435 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0019 | 0/0 | 3432 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| c0020 | 0/0 | 3435 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3118 | 81 | 27 | 18 | 29 | 4 | 2 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0002 | 0/0 | 3119 | 67 | 4 | 14 | 37 | 2 | 10 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0003 | 1/0 | 3119 | 55 | 2 | 19 | 20 | 2 | 11 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0004 | 0/0 | 3119 | 19 | 12 | 6 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0005 | 0/0 | 3119 | 8 | 3 | 2 | 3 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0006 | 0/0 | 3119 | 6 | 6 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0007 | 0/0 | 3119 | 6 | 1 | 2 | 0 | 2 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0008 | 0/0 | 3119 | 6 | 0 | 3 | 0 | 2 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0009 | 0/0 | 3118 | 5 | 1 | 2 | 1 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0010 | 0/0 | 3119 | 5 | 0 | 0 | 5 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0011 | 0/0 | 3120 | 4 | 0 | 0 | 2 | 0 | 2 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0012 | 0/0 | 3120 | 3 | 0 | 2 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0013 | 0/0 | 3119 | 3 | 0 | 1 | 0 | 0 | 2 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0014 | 0/0 | 3118 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0015 | 0/0 | 3120 | 2 | 1 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0016 | 0/0 | 3119 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0017 | 0/0 | 3119 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0018 | 0/0 | 3119 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0019 | 0/0 | 3107 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0020 | 0/0 | 3119 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0021 | 0/0 | 3119 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0022 | 0/0 | 3119 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0023 | 0/0 | 3119 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0024 | 0/0 | 3119 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0025 | 0/0 | 3119 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0026 | 0/0 | 3119 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0027 | 0/0 | 3119 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0028 | 0/0 | 3119 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0029 | 0/0 | 3118 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0030 | 0/0 | 3118 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0031 | 0/0 | 3118 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0032 | 0/0 | 3118 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0033 | 0/0 | 3118 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0034 | 0/0 | 3118 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0035 | 0/0 | 3118 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| t0036 | 0/0 | 3119 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0108 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0123 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3435 | 78 | 27 | 22 | 22 | 4 | 2 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0003 | 1/0 | 3435 | 60 | 2 | 22 | 18 | 5 | 12 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0004 | 0/0 | 3435 | 27 | 15 | 8 | 0 | 1 | 3 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0005 | 0/0 | 3435 | 15 | 2 | 4 | 6 | 2 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0006 | 0/0 | 3435 | 10 | 10 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0009 | 0/0 | 3435 | 3 | 1 | 0 | 2 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0011 | 0/0 | 3435 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0013 | 0/0 | 3435 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0016 | 0/0 | 3435 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0018 | 0/0 | 3435 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0002c0002 | 0/0 | 3432 | 78 | 4 | 14 | 44 | 2 | 14 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0002c0017 | 0/0 | 3432 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0003c0007 | 0/0 | 3435 | 8 | 0 | 0 | 8 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0004c0008 | 0/0 | 3435 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0005c0010 | 0/0 | 3435 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0006c0012 | 0/0 | 3435 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0007c0014 | 0/0 | 3432 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0008c0019 | 0/0 | 3432 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0009c0015 | 0/0 | 3435 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0010c0020 | 0/0 | 3435 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6552 | 69 | 25 | 18 | 19 | 4 | 2 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0001t0005 | 0/0 | 6553 | 7 | 2 | 2 | 3 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0001t0030 | 0/0 | 6552 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0001t0031 | 0/0 | 6552 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0003t0003 | 1/0 | 6553 | 49 | 1 | 18 | 17 | 2 | 10 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0003t0007 | 0/0 | 6553 | 6 | 1 | 2 | 0 | 2 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0003t0012 | 0/0 | 6554 | 3 | 0 | 2 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0003t0018 | 0/0 | 6553 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0003t0019 | 0/0 | 6541 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0004t0004 | 0/0 | 6553 | 19 | 12 | 6 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0004t0013 | 0/0 | 6553 | 3 | 0 | 1 | 0 | 0 | 2 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0004t0015 | 0/0 | 6554 | 2 | 1 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0004t0029 | 0/0 | 6552 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0004t0033 | 0/0 | 6552 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0004t0036 | 0/0 | 6553 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0005t0003 | 0/0 | 6553 | 2 | 1 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0005t0008 | 0/0 | 6553 | 6 | 0 | 3 | 0 | 2 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0005t0010 | 0/0 | 6553 | 5 | 0 | 0 | 5 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0005t0021 | 0/0 | 6553 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0005t0035 | 0/0 | 6552 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0006t0002 | 0/0 | 6553 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0006t0005 | 0/0 | 6553 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0006t0006 | 0/0 | 6553 | 6 | 6 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0006t0022 | 0/0 | 6553 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0009t0001 | 0/0 | 6552 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0009t0002 | 0/0 | 6553 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0009t0028 | 0/0 | 6553 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0011t0016 | 0/0 | 6553 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0013t0003 | 0/0 | 6553 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0016t0020 | 0/0 | 6553 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0001c0018t0032 | 0/0 | 6552 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0002c0002t0002 | 0/0 | 6550 | 61 | 2 | 12 | 36 | 2 | 9 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0002c0002t0009 | 0/0 | 6549 | 5 | 1 | 2 | 1 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0002c0002t0011 | 0/0 | 6551 | 4 | 0 | 0 | 2 | 0 | 2 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0002c0002t0017 | 0/0 | 6550 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0002c0002t0023 | 0/0 | 6550 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0002c0002t0024 | 0/0 | 6550 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0002c0002t0025 | 0/0 | 6550 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0002c0002t0026 | 0/0 | 6550 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0002c0002t0027 | 0/0 | 6550 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0002c0002t0034 | 0/0 | 6549 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0002c0017t0002 | 0/0 | 6550 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0003c0007t0001 | 0/0 | 6552 | 8 | 0 | 0 | 8 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0004c0008t0014 | 0/0 | 6552 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0005c0010t0003 | 0/0 | 6553 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0006c0012t0001 | 0/0 | 6552 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0007c0014t0002 | 0/0 | 6550 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0008c0019t0002 | 0/0 | 6550 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0009c0015t0001 | 0/0 | 6552 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| a0010c0020t0003 | 0/0 | 6553 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | copy fasta | chr5 | 109684927 | 109874625 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0108 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0030g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0001t0031g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0123 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0007g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0007g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0007g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0007g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0007g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0012g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0012g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0012g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0018g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0003t0019g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0013g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0013g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0013g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0015g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0015g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0029g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0033g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0004t0036g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0005t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0005t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0005t0008g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0005t0008g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0005t0008g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0005t0008g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0005t0008g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0005t0008g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0005t0010g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0005t0010g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0005t0010g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0005t0010g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0005t0010g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0005t0021g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0005t0035g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0006t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0006t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0006t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0006t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0006t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0006t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0006t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0006t0006g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0006t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0006t0022g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0009t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0009t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0009t0028g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0011t0016g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0011t0016g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0013t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0016t0020g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0001c0018t0032g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0009g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0009g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0009g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0009g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0011g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0011g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0011g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0011g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0017g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0017g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0023g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0024g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0025g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0026g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0027g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0002t0034g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0002c0017t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0003c0007t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0003c0007t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0003c0007t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0003c0007t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0003c0007t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0003c0007t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0003c0007t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0004c0008t0014g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0004c0008t0014g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0004c0008t0014g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0005c0010t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0006c0012t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0006c0012t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0007c0014t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0008c0019t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0009c0015t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| a0010c0020t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0008 | g0011 | EUR | GBR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0248 | EUR | GBR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00140 | hp1 | a0001 | c0005 | t0008 | g0016 | EUR | GBR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00140 | hp2 | a0001 | c0003 | t0018 | g0144 | EUR | GBR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00438 | hp2 | a0002 | c0002 | t0023 | g0223 | EAS | CHS | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00597 | hp1 | a0001 | c0003 | t0003 | g0162 | EAS | CHS | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0255 | EAS | CHS | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00609 | hp1 | a0003 | c0007 | t0001 | g0194 | EAS | CHS | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00609 | hp2 | a0002 | c0002 | t0025 | g0263 | EAS | CHS | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00639 | hp2 | a0001 | c0005 | t0008 | g0010 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00642 | hp1 | a0002 | c0002 | t0009 | g0215 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00642 | hp2 | a0001 | c0003 | t0003 | g0135 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00673 | hp1 | a0003 | c0007 | t0001 | g0195 | EAS | CHS | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0206 | EAS | CHS | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00733 | hp1 | a0001 | c0003 | t0003 | g0027 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00733 | hp2 | a0002 | c0002 | t0009 | g0270 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0237 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00735 | hp2 | a0001 | c0003 | t0003 | g0146 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0110 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG00741 | hp2 | a0001 | c0003 | t0003 | g0165 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01069 | hp1 | a0001 | c0003 | t0003 | g0145 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01069 | hp2 | a0001 | c0004 | t0015 | g0210 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01071 | hp2 | a0001 | c0004 | t0004 | g0211 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01074 | hp2 | a0001 | c0003 | t0003 | g0134 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01081 | hp2 | a0001 | c0005 | t0008 | g0017 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01106 | hp1 | a0001 | c0004 | t0004 | g0036 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01106 | hp2 | a0001 | c0003 | t0007 | g0177 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01109 | hp1 | a0001 | c0003 | t0003 | g0125 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01109 | hp2 | a0001 | c0005 | t0003 | g0054 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01167 | hp1 | a0001 | c0003 | t0003 | g0213 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01168 | hp1 | a0001 | c0004 | t0004 | g0030 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01168 | hp2 | a0001 | c0003 | t0007 | g0141 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01169 | hp2 | a0001 | c0004 | t0004 | g0031 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01175 | hp1 | a0001 | c0004 | t0004 | g0037 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01175 | hp2 | a0001 | c0003 | t0012 | g0166 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01192 | hp1 | a0001 | c0004 | t0013 | g0282 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01192 | hp2 | a0001 | c0003 | t0003 | g0159 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01243 | hp1 | a0001 | c0004 | t0004 | g0046 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01255 | hp1 | a0001 | c0003 | t0003 | g0164 | AMR | CLM | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01256 | hp1 | a0001 | c0003 | t0003 | g0138 | AMR | CLM | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01257 | hp1 | a0001 | c0001 | t0030 | g0085 | AMR | CLM | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01257 | hp2 | a0001 | c0003 | t0003 | g0129 | AMR | CLM | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01346 | hp2 | a0001 | c0003 | t0003 | g0124 | AMR | CLM | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01361 | hp2 | a0002 | c0017 | t0002 | g0101 | AMR | CLM | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01433 | hp1 | a0001 | c0003 | t0012 | g0168 | AMR | CLM | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0258 | AMR | CLM | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01515 | hp2 | a0001 | c0003 | t0007 | g0140 | EUR | IBS | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01516 | hp1 | a0001 | c0004 | t0033 | g0032 | EUR | IBS | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01516 | hp2 | a0001 | c0003 | t0003 | g0170 | EUR | IBS | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01517 | hp1 | a0001 | c0003 | t0003 | g0171 | EUR | IBS | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0105 | AFR | ACB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01891 | hp2 | a0001 | c0006 | t0002 | g0279 | AFR | ACB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01928 | hp2 | a0001 | c0003 | t0003 | g0156 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0239 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01934 | hp2 | a0001 | c0001 | t0031 | g0122 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01943 | hp2 | a0001 | c0003 | t0003 | g0209 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01952 | hp2 | a0001 | c0003 | t0003 | g0201 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0256 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01975 | hp2 | a0007 | c0014 | t0002 | g0193 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0236 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0243 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0269 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02027 | hp1 | a0001 | c0005 | t0010 | g0020 | EAS | KHV | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0252 | EAS | KHV | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02040 | hp1 | a0003 | c0007 | t0001 | g0199 | EAS | KHV | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02040 | hp2 | a0001 | c0009 | t0001 | g0208 | EAS | KHV | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02055 | hp1 | a0001 | c0011 | t0016 | g0026 | AFR | ACB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02056 | hp1 | a0001 | c0003 | t0003 | g0167 | EAS | KHV | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0240 | EAS | KHV | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0244 | EAS | KHV | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0220 | EAS | KHV | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02132 | hp1 | a0001 | c0003 | t0003 | g0158 | EAS | KHV | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | KHV | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02135 | hp2 | a0002 | c0002 | t0011 | g0261 | EAS | KHV | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02145 | hp1 | a0001 | c0003 | t0003 | g0131 | AFR | ACB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0251 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0289 | EAS | CDX | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CDX | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0284 | AFR | ACB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02257 | hp2 | a0001 | c0005 | t0003 | g0169 | AFR | ACB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02258 | hp2 | a0001 | c0004 | t0029 | g0052 | AFR | ACB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02273 | hp1 | a0001 | c0003 | t0003 | g0157 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0257 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02280 | hp1 | a0001 | c0004 | t0004 | g0001 | AFR | ACB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0245 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02293 | hp2 | a0001 | c0003 | t0003 | g0173 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0178 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02300 | hp2 | a0001 | c0005 | t0008 | g0012 | AMR | PEL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02451 | hp2 | a0001 | c0006 | t0002 | g0278 | AFR | ACB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02523 | hp1 | a0003 | c0007 | t0001 | g0005 | EAS | KHV | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0253 | EAS | KHV | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02630 | hp1 | a0001 | c0004 | t0004 | g0034 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02647 | hp2 | a0001 | c0009 | t0028 | g0008 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02717 | hp1 | a0004 | c0008 | t0014 | g0023 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02717 | hp2 | a0001 | c0004 | t0004 | g0048 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0241 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02735 | hp2 | a0001 | c0003 | t0003 | g0142 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02738 | hp1 | a0001 | c0003 | t0003 | g0137 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02738 | hp2 | a0002 | c0002 | t0011 | g0268 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02809 | hp2 | a0001 | c0004 | t0036 | g0024 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02895 | hp1 | a0001 | c0006 | t0006 | g0288 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02895 | hp2 | a0001 | c0005 | t0035 | g0013 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02896 | hp2 | a0001 | c0004 | t0004 | g0053 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02897 | hp2 | a0001 | c0006 | t0006 | g0287 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02922 | hp2 | a0001 | c0004 | t0004 | g0001 | AFR | ESN | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0212 | AFR | ESN | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03017 | hp1 | a0001 | c0004 | t0013 | g0049 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0267 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03041 | hp1 | a0001 | c0004 | t0004 | g0051 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03041 | hp2 | a0004 | c0008 | t0014 | g0022 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03098 | hp2 | a0001 | c0004 | t0004 | g0041 | AFR | MSL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03130 | hp1 | a0001 | c0006 | t0006 | g0285 | AFR | ESN | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03139 | hp1 | a0001 | c0011 | t0016 | g0025 | AFR | ESN | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0099 | AFR | ESN | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03195 | hp2 | a0001 | c0006 | t0006 | g0172 | AFR | ESN | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03209 | hp1 | a0001 | c0004 | t0004 | g0044 | AFR | MSL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03225 | hp2 | a0001 | c0006 | t0022 | g0035 | AFR | MSL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0283 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03239 | hp2 | a0002 | c0002 | t0034 | g0218 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03453 | hp1 | a0001 | c0016 | t0020 | g0112 | AFR | MSL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03453 | hp2 | a0001 | c0006 | t0006 | g0286 | AFR | MSL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03486 | hp1 | a0001 | c0006 | t0006 | g0038 | AFR | MSL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03486 | hp2 | a0006 | c0012 | t0001 | g0028 | AFR | MSL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03490 | hp1 | a0001 | c0003 | t0003 | g0143 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03491 | hp1 | a0001 | c0003 | t0003 | g0130 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0242 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03492 | hp2 | a0001 | c0003 | t0003 | g0132 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03516 | hp1 | a0001 | c0018 | t0032 | g0084 | AFR | ESN | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03516 | hp2 | a0004 | c0008 | t0014 | g0021 | AFR | ESN | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03579 | hp2 | a0002 | c0002 | t0027 | g0234 | AFR | MSL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03654 | hp1 | a0001 | c0004 | t0004 | g0033 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0189 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03669 | hp1 | a0001 | c0005 | t0008 | g0009 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03669 | hp2 | a0001 | c0003 | t0003 | g0133 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03704 | hp1 | a0002 | c0002 | t0011 | g0179 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03704 | hp2 | a0001 | c0013 | t0003 | g0155 | SAS | PJL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03834 | hp1 | a0001 | c0003 | t0019 | g0180 | SAS | BEB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0266 | SAS | BEB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03927 | hp1 | a0001 | c0003 | t0003 | g0139 | SAS | BEB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03927 | hp2 | a0002 | c0002 | t0009 | g0217 | SAS | BEB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03942 | hp1 | a0001 | c0003 | t0003 | g0128 | SAS | BEB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03942 | hp2 | a0008 | c0019 | t0002 | g0250 | SAS | BEB | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG04115 | hp1 | a0001 | c0003 | t0003 | g0127 | SAS | STU | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0265 | SAS | STU | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG04199 | hp1 | a0001 | c0003 | t0007 | g0050 | SAS | STU | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0229 | SAS | STU | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0230 | SAS | STU | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG04228 | hp2 | a0001 | c0004 | t0013 | g0214 | SAS | STU | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18906 | hp1 | a0006 | c0012 | t0001 | g0029 | AFR | YRI | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18906 | hp2 | a0001 | c0004 | t0004 | g0043 | AFR | YRI | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18942 | hp2 | a0001 | c0003 | t0003 | g0147 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18944 | hp2 | a0001 | c0005 | t0010 | g0019 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0221 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18945 | hp2 | a0001 | c0003 | t0003 | g0152 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18947 | hp1 | a0001 | c0003 | t0003 | g0207 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18949 | hp2 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18952 | hp2 | a0002 | c0002 | t0026 | g0231 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18956 | hp1 | a0009 | c0015 | t0001 | g0075 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18957 | hp1 | a0001 | c0003 | t0003 | g0150 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18959 | hp1 | a0001 | c0005 | t0010 | g0014 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18959 | hp2 | a0002 | c0002 | t0017 | g0275 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18962 | hp1 | a0002 | c0002 | t0009 | g0200 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18962 | hp2 | a0003 | c0007 | t0001 | g0197 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18965 | hp1 | a0001 | c0003 | t0012 | g0153 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18966 | hp2 | a0001 | c0003 | t0003 | g0160 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18969 | hp2 | a0001 | c0003 | t0003 | g0151 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18975 | hp2 | a0001 | c0003 | t0003 | g0126 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18981 | hp1 | a0005 | c0010 | t0003 | g0004 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18982 | hp1 | a0001 | c0003 | t0003 | g0149 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18983 | hp1 | a0002 | c0002 | t0017 | g0276 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0260 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18991 | hp1 | a0003 | c0007 | t0001 | g0198 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18991 | hp2 | a0001 | c0005 | t0021 | g0262 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18998 | hp1 | a0002 | c0002 | t0011 | g0181 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18998 | hp2 | a0001 | c0003 | t0003 | g0161 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19000 | hp2 | a0001 | c0003 | t0003 | g0154 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19003 | hp2 | a0003 | c0007 | t0001 | g0196 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19007 | hp2 | a0001 | c0003 | t0003 | g0187 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19009 | hp1 | a0001 | c0005 | t0010 | g0018 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19030 | hp1 | a0001 | c0004 | t0004 | g0045 | AFR | LWK | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19043 | hp1 | a0001 | c0004 | t0015 | g0040 | AFR | LWK | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19043 | hp2 | a0002 | c0002 | t0009 | g0007 | AFR | LWK | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0264 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19058 | hp1 | a0005 | c0010 | t0003 | g0004 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19060 | hp1 | a0010 | c0020 | t0003 | g0174 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19064 | hp1 | a0001 | c0005 | t0010 | g0015 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19064 | hp2 | a0001 | c0003 | t0003 | g0163 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0235 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0226 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19085 | hp2 | a0001 | c0003 | t0003 | g0185 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19089 | hp2 | a0001 | c0003 | t0003 | g0148 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19240 | hp1 | a0001 | c0004 | t0004 | g0042 | AFR | YRI | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | YRI | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0259 | EUR | TSI | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | TSI | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA20805 | hp1 | a0001 | c0003 | t0007 | g0136 | EUR | TSI | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA20905 | hp1 | a0001 | c0003 | t0003 | g0192 | SAS | GIH | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA20905 | hp2 | a0002 | c0002 | t0024 | g0233 | SAS | GIH | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0280 | AMR | CLM | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0111 | AMR | CLM | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03471 | hp1 | a0001 | c0003 | t0007 | g0176 | AFR | MSL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG03471 | hp2 | a0001 | c0004 | t0004 | g0047 | AFR | MSL | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | USA | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| HG06807 | hp2 | a0001 | c0006 | t0005 | g0281 | AFR | USA | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18955 | hp1 | a0001 | c0009 | t0002 | g0227 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| NA18955 | hp2 | a0003 | c0007 | t0001 | g0005 | EAS | JPT | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0108 | REF | REF | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0003 | g0123 | REF | REF | MAN2A1_chr5_109684927_109874625 | MAN2A1 | chr5 | 109684927 | 109874625 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:109713722
|
C | A | 1 | a0005 | 2 | NA18981.hp1 NA19058.hp1 |
missense_variant | MODERATE | c.338C>A | p.Thr113Asn | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/22 | 829/6553 | 338/3435 | 113/1144 | chr5 | 109713722 | ||
| chr5:109767648
|
G | T | 1 | a0010 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.949G>T | p.Ala317Ser | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/22 | 1440/6553 | 949/3435 | 317/1144 | chr5 | 109767648 | ||
| chr5:109817383
|
T | C | 2 | a0003a0007 | 9 | HG00609.hp1 HG00673.hp1 HG01975.hp2 others(6): Show |
missense_variant | MODERATE | c.2054T>C | p.Val685Ala | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/22 | 2545/6553 | 2054/3435 | 685/1144 | chr5 | 109817383 | ||
| chr5:109819719
|
T | G | 1 | a0009 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.2160T>G | p.Ile720Met | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 14/22 | 2651/6553 | 2160/3435 | 720/1144 | chr5 | 109819719 | ||
| chr5:109820306
|
T | A | 1 | a0009 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.2415T>A | p.Ser805Arg | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/22 | 2906/6553 | 2415/3435 | 805/1144 | chr5 | 109820306 | ||
| chr5:109823793
|
T | A | 1 | a0004 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.2522T>A | p.Phe841Tyr | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/22 | 3013/6553 | 2522/3435 | 841/1144 | chr5 | 109823793 | ||
| chr5:109855234
|
TCTC | T | 3 | a0002a0007a0008 | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
disruptive_inframe_deletion | MODERATE | c.3075_3077delCTC | p.Ser1026del | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/22 | 3566/6553 | 3075/3435 | 1025/1144 | INFO_REALIGN_3_PRIME | chr5 | 109855234 | |
| chr5:109855242
|
C | T | 1 | a0004 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.3079C>T | p.Pro1027Ser | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/22 | 3570/6553 | 3079/3435 | 1027/1144 | chr5 | 109855242 | ||
| chr5:109866963
|
A | G | 1 | a0008 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.3400A>G | p.Met1134Val | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 3891/6553 | 3400/3435 | 1134/1144 | chr5 | 109866963 | ||
| chr5:109866969
|
A | G | 1 | a0006 | 2 | HG03486.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.3406A>G | p.Ile1136Val | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 3897/6553 | 3406/3435 | 1136/1144 | chr5 | 109866969 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:109716239
|
G | A | 1 | a0001c0013 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.510G>A | p.Val170Val | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/22 | 1001/6553 | 510/3435 | 170/1144 | chr5 | 109716239 | ||
| chr5:109774836
|
T | A | 9 | a0001c0001a0001c0011a0001c0016others(6): Show | 95 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(92): Show |
synonymous_variant | LOW | c.1245T>A | p.Arg415Arg | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/22 | 1736/6553 | 1245/3435 | 415/1144 | chr5 | 109774836 | ||
| chr5:109774890
|
G | A | 2 | a0001c0005a0001c0006 | 25 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(22): Show |
synonymous_variant | LOW | c.1299G>A | p.Thr433Thr | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/22 | 1790/6553 | 1299/3435 | 433/1144 | chr5 | 109774890 | ||
| chr5:109781470
|
A | G | 3 | a0001c0009a0002c0002a0008c0019 | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
synonymous_variant | LOW | c.1449A>G | p.Gln483Gln | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/22 | 1940/6553 | 1449/3435 | 483/1144 | chr5 | 109781470 | ||
| chr5:109817288
|
T | C | 1 | a0001c0011 | 2 | HG02055.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.1959T>C | p.Tyr653Tyr | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/22 | 2450/6553 | 1959/3435 | 653/1144 | chr5 | 109817288 | ||
| chr5:109845981
|
A | T | 14 | a0001c0001a0001c0004a0001c0006others(11): Show | 216 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(213): Show |
synonymous_variant | LOW | c.2817A>T | p.Ser939Ser | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 18/22 | 3308/6553 | 2817/3435 | 939/1144 | chr5 | 109845981 | ||
| chr5:109855241
|
A | G | 1 | a0001c0018 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.3078A>G | p.Ser1026Ser | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/22 | 3569/6553 | 3078/3435 | 1026/1144 | chr5 | 109855241 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:109689998
|
G | C | 1 | a0001c0003t0018 | 1 | HG00140.hp2 | 5_prime_UTR_variant | MODIFIER | c.-420G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/22 | 420 | chr5 | 109689998 | |||||
| chr5:109690011
|
A | G | 1 | a0001c0004t0036 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-407A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/22 | 407 | chr5 | 109690011 | |||||
| chr5:109690115
|
C | G | 3 | a0001c0005t0008a0001c0005t0010a0001c0005t0035 | 12 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-303C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/22 | 303 | chr5 | 109690115 | |||||
| chr5:109690217
|
CAGGCCAG others(5): Show |
C | 1 | a0001c0003t0019 | 1 | HG03834.hp1 | 5_prime_UTR_variant | MODIFIER | c.-194_-183delGGGCGA others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/22 | 183 | INFO_REALIGN_3_PRIME | chr5 | 109690217 | ||||
| chr5:109867022
|
A | G | 1 | a0004c0008t0014 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*24A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 24 | chr5 | 109867022 | |||||
| chr5:109867024
|
A | G | 1 | a0001c0003t0007 | 6 | HG01106.hp2 HG01168.hp2 HG01515.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*26A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 26 | chr5 | 109867024 | |||||
| chr5:109867157
|
G | GA | 3 | a0001c0003t0012a0001c0004t0015a0002c0002t0011 | 9 | HG01069.hp2 HG01175.hp2 HG01433.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*180dupA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 181 | INFO_REALIGN_3_PRIME | chr5 | 109867157 | ||||
| chr5:109867157
|
GA | G | 14 | a0001c0001t0001a0001c0001t0030a0001c0001t0031others(11): Show | 96 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*180delA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 180 | INFO_REALIGN_3_PRIME | chr5 | 109867157 | ||||
| chr5:109867194
|
A | G | 1 | a0001c0009t0028 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*196A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 196 | chr5 | 109867194 | |||||
| chr5:109867341
|
G | A | 10 | a0001c0001t0001a0001c0001t0005a0001c0001t0030others(7): Show | 92 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*343G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 343 | chr5 | 109867341 | |||||
| chr5:109867595
|
A | G | 17 | a0001c0004t0036a0001c0006t0002a0001c0009t0002others(14): Show | 86 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*597A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 597 | chr5 | 109867595 | |||||
| chr5:109867930
|
A | G | 1 | a0002c0002t0027 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*932A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 932 | chr5 | 109867930 | |||||
| chr5:109868016
|
A | G | 1 | a0001c0001t0031 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1018A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 1018 | chr5 | 109868016 | |||||
| chr5:109868017
|
C | T | 1 | a0001c0006t0022 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1019C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 1019 | chr5 | 109868017 | |||||
| chr5:109868220
|
C | T | 17 | a0001c0004t0036a0001c0006t0002a0001c0009t0002others(14): Show | 86 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1222C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 1222 | chr5 | 109868220 | |||||
| chr5:109868227
|
A | G | 1 | a0002c0002t0026 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1229A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 1229 | chr5 | 109868227 | |||||
| chr5:109868323
|
G | A | 36 | a0001c0001t0001a0001c0001t0005a0001c0001t0030others(33): Show | 216 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*1325G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 1325 | chr5 | 109868323 | |||||
| chr5:109868337
|
T | C | 1 | a0001c0004t0029 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1339T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 1339 | chr5 | 109868337 | |||||
| chr5:109868356
|
T | A | 5 | a0001c0006t0006a0001c0006t0022a0001c0011t0016others(2): Show | 13 | HG02055.hp1 HG02717.hp1 HG02895.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1358T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 1358 | chr5 | 109868356 | |||||
| chr5:109868369
|
T | A | 1 | a0002c0002t0017 | 2 | NA18959.hp2 NA18983.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1371T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 1371 | chr5 | 109868369 | |||||
| chr5:109868380
|
T | C | 1 | a0001c0016t0020 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1382T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 1382 | chr5 | 109868380 | |||||
| chr5:109868406
|
G | T | 37 | a0001c0001t0001a0001c0001t0005a0001c0001t0030others(34): Show | 217 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*1408G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 1408 | chr5 | 109868406 | |||||
| chr5:109868669
|
A | T | 1 | a0001c0011t0016 | 2 | HG02055.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1671A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 1671 | chr5 | 109868669 | |||||
| chr5:109868740
|
T | C | 1 | a0002c0002t0023 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1742T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 1742 | chr5 | 109868740 | |||||
| chr5:109868780
|
G | A | 1 | a0002c0002t0024 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1782G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 1782 | chr5 | 109868780 | |||||
| chr5:109868791
|
C | T | 1 | a0002c0002t0034 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1793C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 1793 | chr5 | 109868791 | |||||
| chr5:109868975
|
C | G | 2 | a0001c0005t0010a0001c0005t0021 | 6 | HG02027.hp1 NA18944.hp2 NA18959.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1977C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 1977 | chr5 | 109868975 | |||||
| chr5:109869157
|
A | G | 1 | a0001c0004t0013 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2159A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 2159 | chr5 | 109869157 | |||||
| chr5:109869255
|
G | A | 1 | a0001c0001t0030 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2257G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 2257 | chr5 | 109869255 | |||||
| chr5:109869352
|
C | T | 1 | a0002c0002t0025 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2354C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 22/22 | 2354 | chr5 | 109869352 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:109690738
|
G | C | 1 | a0002c0002t0009g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.135+186G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109690738 | ||||||
| chr5:109690784
|
C | G | 92 | a0001c0001t0001g0290a0001c0003t0003g0201a0001c0003t0003g0207others(89): Show | 93 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.135+232C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109690784 | ||||||
| chr5:109690949
|
G | C | 1 | a0001c0003t0003g0201 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.135+397G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109690949 | ||||||
| chr5:109690962
|
G | C | 138 | a0001c0001t0001g0039a0001c0003t0003g0027a0001c0003t0003g0201others(135): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.135+410G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109690962 | ||||||
| chr5:109690971
|
C | T | 3 | a0001c0004t0004g0051a0001c0004t0004g0053a0001c0004t0029g0052 | 3 | HG02258.hp2 HG02896.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.135+419C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109690971 | ||||||
| chr5:109690991
|
G | C | 13 | a0001c0005t0008g0009a0001c0005t0008g0010a0001c0005t0008g0011others(10): Show | 13 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.135+439G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109690991 | ||||||
| chr5:109691014
|
T | A | 1 | a0001c0005t0003g0054 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.135+462T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109691014 | ||||||
| chr5:109691130
|
C | T | 9 | a0002c0002t0009g0200a0003c0007t0001g0005a0003c0007t0001g0194others(6): Show | 10 | HG00609.hp1 HG00673.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.135+578C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109691130 | ||||||
| chr5:109691264
|
A | G | 2 | a0001c0003t0007g0050a0001c0004t0013g0049 | 2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.135+712A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109691264 | ||||||
| chr5:109691381
|
C | T | 42 | a0001c0001t0001g0039a0001c0003t0003g0027a0001c0004t0004g0001others(39): Show | 43 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.135+829C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109691381 | ||||||
| chr5:109691731
|
G | C | 3 | a0002c0002t0002g0202a0002c0002t0002g0203a0002c0002t0002g0204 | 3 | NA18957.hp2 NA18969.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.135+1179G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109691731 | ||||||
| chr5:109691759
|
A | G | 1 | a0002c0002t0002g0289 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.135+1207A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109691759 | ||||||
| chr5:109691856
|
C | T | 12 | a0001c0005t0008g0009a0001c0005t0008g0010a0001c0005t0008g0011others(9): Show | 12 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.135+1304C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109691856 | ||||||
| chr5:109691893
|
T | G | 1 | a0002c0002t0002g0205 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.135+1341T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109691893 | ||||||
| chr5:109691925
|
T | C | 12 | a0001c0005t0008g0009a0001c0005t0008g0010a0001c0005t0008g0011others(9): Show | 12 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.135+1373T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109691925 | ||||||
| chr5:109691934
|
G | A | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.135+1382G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109691934 | ||||||
| chr5:109691972
|
C | T | 14 | a0001c0001t0001g0039a0001c0004t0004g0001a0001c0004t0004g0041others(11): Show | 15 | HG01243.hp1 HG02258.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+1420C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109691972 | ||||||
| chr5:109692109
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.135+1557C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109692109 | ||||||
| chr5:109692150
|
C | T | 49 | a0001c0001t0001g0039a0001c0003t0003g0027a0001c0004t0004g0001others(46): Show | 50 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.135+1598C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109692150 | ||||||
| chr5:109692178
|
C | T | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.135+1626C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109692178 | ||||||
| chr5:109692225
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.135+1673C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109692225 | ||||||
| chr5:109692643
|
A | G | 35 | a0001c0003t0003g0027a0001c0004t0004g0030a0001c0004t0004g0031others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.135+2091A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109692643 | ||||||
| chr5:109692697
|
A | C | 1 | a0002c0002t0002g0280 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.135+2145A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109692697 | ||||||
| chr5:109692724
|
G | A | 35 | a0001c0003t0003g0027a0001c0004t0004g0030a0001c0004t0004g0031others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.135+2172G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109692724 | ||||||
| chr5:109692735
|
C | A | 2 | a0001c0003t0007g0050a0001c0004t0013g0049 | 2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.135+2183C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109692735 | ||||||
| chr5:109692746
|
G | A | 12 | a0001c0005t0008g0009a0001c0005t0008g0010a0001c0005t0008g0011others(9): Show | 12 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.135+2194G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109692746 | ||||||
| chr5:109692775
|
T | G | 1 | a0002c0002t0002g0206 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.135+2223T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109692775 | ||||||
| chr5:109692783
|
C | T | 1 | a0001c0003t0003g0192 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.135+2231C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109692783 | ||||||
| chr5:109692787
|
CA | C | 9 | a0001c0004t0013g0282a0001c0006t0005g0281a0001c0006t0006g0285others(6): Show | 9 | HG01192.hp1 HG02257.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+2236delA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109692787 | ||||||
| chr5:109692900
|
C | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01346.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.135+2348C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109692900 | ||||||
| chr5:109693112
|
C | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+2560C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109693112 | ||||||
| chr5:109693185
|
AC | A | 125 | a0001c0001t0001g0188a0001c0003t0003g0027a0001c0003t0003g0201others(122): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.135+2636delC | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109693185 | |||||
| chr5:109693188
|
C | G | 1 | a0001c0003t0003g0187 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.135+2636C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109693188 | ||||||
| chr5:109693270
|
T | A | 1 | a0001c0004t0013g0049 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.135+2718T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109693270 | ||||||
| chr5:109693463
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.135+2911C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109693463 | ||||||
| chr5:109693572
|
C | T | 1 | a0001c0006t0006g0038 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.135+3020C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109693572 | ||||||
| chr5:109693623
|
A | G | 3 | a0001c0004t0004g0051a0001c0004t0004g0053a0001c0004t0029g0052 | 3 | HG02258.hp2 HG02896.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.135+3071A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109693623 | ||||||
| chr5:109693664
|
A | T | 1 | a0001c0003t0003g0185 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.135+3112A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109693664 | ||||||
| chr5:109693759
|
G | A | 1 | a0001c0006t0006g0038 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.135+3207G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109693759 | ||||||
| chr5:109693909
|
A | G | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.135+3357A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109693909 | ||||||
| chr5:109693934
|
T | C | 1 | a0001c0009t0001g0208 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.135+3382T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109693934 | ||||||
| chr5:109694116
|
G | A | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.135+3564G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109694116 | ||||||
| chr5:109694167
|
C | T | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG01167.hp2 HG01169.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.135+3615C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109694167 | ||||||
| chr5:109694222
|
G | A | 1 | a0002c0002t0002g0289 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.135+3670G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109694222 | ||||||
| chr5:109694331
|
A | G | 2 | a0001c0005t0010g0019a0001c0005t0010g0020 | 2 | HG02027.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.135+3779A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109694331 | ||||||
| chr5:109694340
|
C | G | 93 | a0001c0001t0001g0290a0001c0003t0003g0201a0001c0003t0003g0213others(90): Show | 94 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.135+3788C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109694340 | ||||||
| chr5:109694347
|
T | C | 3 | a0001c0004t0004g0051a0001c0004t0004g0053a0001c0004t0029g0052 | 3 | HG02258.hp2 HG02896.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.135+3795T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109694347 | ||||||
| chr5:109694426
|
C | G | 1 | a0001c0001t0001g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.135+3874C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109694426 | ||||||
| chr5:109694447
|
C | T | 1 | a0010c0020t0003g0174 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.135+3895C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109694447 | ||||||
| chr5:109694551
|
T | C | 4 | a0003c0007t0001g0194a0003c0007t0001g0195a0003c0007t0001g0196others(1): Show | 4 | HG00609.hp1 HG00673.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+3999T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109694551 | ||||||
| chr5:109694593
|
C | T | 1 | a0001c0003t0003g0173 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.135+4041C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109694593 | ||||||
| chr5:109694658
|
G | GT | 105 | a0001c0001t0001g0290a0001c0003t0003g0170a0001c0003t0003g0171others(102): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.135+4118dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109694658 | |||||
| chr5:109694658
|
G | GTT | 25 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(22): Show | 26 | HG00673.hp2 HG01106.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.135+4117_135+4118d others(4): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109694658 | |||||
| chr5:109694779
|
A | G | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.135+4227A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109694779 | ||||||
| chr5:109694958
|
A | G | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.135+4406A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109694958 | ||||||
| chr5:109694975
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.135+4423G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109694975 | ||||||
| chr5:109695298
|
A | G | 2 | a0001c0004t0004g0036a0001c0004t0004g0037 | 2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.135+4746A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109695298 | ||||||
| chr5:109695819
|
T | G | 2 | a0001c0001t0001g0039a0001c0004t0036g0024 | 2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.135+5267T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109695819 | ||||||
| chr5:109696024
|
A | G | 8 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(5): Show | 8 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+5472A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109696024 | ||||||
| chr5:109696186
|
C | T | 1 | a0002c0002t0009g0270 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.135+5634C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109696186 | ||||||
| chr5:109696226
|
G | A | 2 | a0001c0004t0004g0030a0001c0004t0004g0031 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.135+5674G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109696226 | ||||||
| chr5:109696291
|
G | C | 28 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(25): Show | 29 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.135+5739G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109696291 | ||||||
| chr5:109696350
|
T | C | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(223): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.135+5798T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109696350 | ||||||
| chr5:109696387
|
C | T | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.135+5835C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109696387 | ||||||
| chr5:109696390
|
C | T | 1 | a0001c0001t0031g0122 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.135+5838C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109696390 | ||||||
| chr5:109696496
|
C | T | 13 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(10): Show | 14 | HG01243.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.135+5944C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109696496 | ||||||
| chr5:109696523
|
A | G | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.135+5971A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109696523 | ||||||
| chr5:109696635
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.135+6083A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109696635 | ||||||
| chr5:109696816
|
G | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(90): Show | 96 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.135+6264G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109696816 | ||||||
| chr5:109696832
|
A | G | 1 | a0002c0002t0011g0181 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.135+6280A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109696832 | ||||||
| chr5:109696995
|
A | G | 8 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(5): Show | 8 | HG01255.hp2 HG01361.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+6443A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109696995 | ||||||
| chr5:109697049
|
G | C | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.135+6497G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109697049 | ||||||
| chr5:109697123
|
C | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(86): Show | 92 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.135+6571C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109697123 | ||||||
| chr5:109697176
|
T | G | 4 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+6624T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109697176 | ||||||
| chr5:109697692
|
A | G | 85 | a0001c0001t0001g0290a0001c0003t0003g0201a0001c0003t0019g0180others(82): Show | 86 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.135+7140A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109697692 | ||||||
| chr5:109697745
|
A | G | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+7193A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109697745 | ||||||
| chr5:109697800
|
A | T | 2 | a0001c0004t0004g0047a0001c0004t0004g0048 | 2 | HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.135+7248A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109697800 | ||||||
| chr5:109697842
|
G | C | 1 | a0001c0001t0001g0082 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.135+7290G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109697842 | ||||||
| chr5:109697854
|
G | C | 1 | a0001c0001t0001g0078 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.135+7302G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109697854 | ||||||
| chr5:109698198
|
C | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.135+7646C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109698198 | ||||||
| chr5:109698476
|
A | G | 20 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(17): Show | 21 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.135+7924A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109698476 | ||||||
| chr5:109698491
|
T | A | 2 | a0001c0005t0003g0054a0001c0005t0003g0169 | 2 | HG01109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.135+7939T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109698491 | ||||||
| chr5:109698514
|
G | GGT | 43 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(40): Show | 44 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.135+7963_135+7964d others(4): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109698514 | |||||
| chr5:109698604
|
C | T | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.135+8052C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109698604 | ||||||
| chr5:109698681
|
T | C | 85 | a0001c0001t0001g0290a0001c0003t0003g0201a0001c0003t0019g0180others(82): Show | 86 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.135+8129T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109698681 | ||||||
| chr5:109698914
|
C | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(88): Show | 94 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.135+8362C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109698914 | ||||||
| chr5:109698991
|
A | G | 1 | a0001c0016t0020g0112 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.135+8439A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109698991 | ||||||
| chr5:109699255
|
T | C | 1 | a0002c0002t0009g0215 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.135+8703T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109699255 | ||||||
| chr5:109699320
|
A | G | 1 | a0001c0003t0007g0177 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.135+8768A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109699320 | ||||||
| chr5:109699347
|
A | G | 20 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(17): Show | 21 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.135+8795A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109699347 | ||||||
| chr5:109699409
|
T | C | 1 | a0001c0004t0015g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.135+8857T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109699409 | ||||||
| chr5:109699433
|
C | A | 1 | a0001c0001t0001g0083 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.135+8881C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109699433 | ||||||
| chr5:109699434
|
A | AT | 289 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.135+8883dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109699434 | |||||
| chr5:109699601
|
T | TAAAG | 130 | a0001c0001t0001g0290a0001c0003t0003g0201a0001c0003t0019g0180others(127): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.135+9050_135+9051i others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109699601 | |||||
| chr5:109699601
|
T | TAGAG | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(95): Show | 101 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.135+9050_135+9053d others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109699601 | |||||
| chr5:109699629
|
G | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(89): Show | 95 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.135+9077G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109699629 | ||||||
| chr5:109699717
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.135+9165G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109699717 | ||||||
| chr5:109699795
|
A | G | 84 | a0001c0001t0001g0290a0001c0003t0019g0180a0001c0005t0021g0262others(81): Show | 85 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.135+9243A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109699795 | ||||||
| chr5:109699864
|
T | TA | 14 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.135+9320dupA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109699864 | |||||
| chr5:109699905
|
A | T | 2 | a0001c0004t0004g0036a0001c0004t0004g0037 | 2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.135+9353A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109699905 | ||||||
| chr5:109699971
|
A | G | 1 | a0001c0001t0005g0111 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.135+9419A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109699971 | ||||||
| chr5:109700055
|
A | G | 1 | a0002c0002t0002g0269 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.135+9503A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109700055 | ||||||
| chr5:109700097
|
T | C | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.135+9545T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109700097 | ||||||
| chr5:109700097
|
T | G | 83 | a0001c0001t0001g0290a0001c0005t0021g0262a0001c0009t0001g0208others(80): Show | 84 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.135+9545T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109700097 | ||||||
| chr5:109700130
|
C | T | 14 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.135+9578C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109700130 | ||||||
| chr5:109700281
|
G | GT | 6 | a0001c0003t0003g0167a0001c0003t0003g0173a0001c0003t0012g0166others(3): Show | 6 | HG01175.hp2 HG01433.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+9746dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109700281 | |||||
| chr5:109700281
|
GT | G | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0055others(196): Show | 204 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.135+9746delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109700281 | |||||
| chr5:109700283
|
T | A | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+9731T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109700283 | ||||||
| chr5:109700316
|
G | A | 1 | a0001c0003t0003g0209 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.135+9764G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109700316 | ||||||
| chr5:109700365
|
C | T | 83 | a0001c0001t0001g0290a0001c0005t0021g0262a0001c0009t0001g0208others(80): Show | 84 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.135+9813C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109700365 | ||||||
| chr5:109700435
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.135+9883C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109700435 | ||||||
| chr5:109700485
|
C | G | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.135+9933C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109700485 | ||||||
| chr5:109700516
|
G | A | 1 | a0002c0002t0002g0216 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.135+9964G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109700516 | ||||||
| chr5:109700533
|
A | C | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(223): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.135+9981A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109700533 | ||||||
| chr5:109700642
|
AAAG | A | 3 | a0001c0004t0036g0024a0001c0006t0002g0278a0001c0006t0002g0279 | 3 | HG01891.hp2 HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.135+10091_135+1009 others(7): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109700642 | ||||||
| chr5:109700790
|
A | T | 1 | a0002c0002t0009g0270 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.135+10238A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109700790 | ||||||
| chr5:109700803
|
C | G | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.135+10251C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109700803 | ||||||
| chr5:109700813
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.135+10261A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109700813 | ||||||
| chr5:109700966
|
G | C | 2 | a0001c0005t0003g0054a0001c0005t0003g0169 | 2 | HG01109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.135+10414G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109700966 | ||||||
| chr5:109701005
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.135+10453G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109701005 | ||||||
| chr5:109701052
|
G | T | 4 | a0002c0002t0002g0265a0002c0002t0002g0266a0002c0002t0002g0267others(1): Show | 4 | HG02738.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+10500G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109701052 | ||||||
| chr5:109701201
|
A | T | 2 | a0001c0005t0008g0016a0001c0005t0008g0017 | 2 | HG00140.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.135+10649A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109701201 | ||||||
| chr5:109701336
|
G | A | 14 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.135+10784G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109701336 | ||||||
| chr5:109701336
|
G | C | 8 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(5): Show | 8 | HG01255.hp2 HG01361.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+10784G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109701336 | ||||||
| chr5:109701337
|
C | T | 81 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.135+10785C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109701337 | ||||||
| chr5:109701351
|
G | T | 1 | a0002c0002t0002g0264 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.135+10799G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109701351 | ||||||
| chr5:109701376
|
T | C | 16 | a0002c0002t0002g0205a0002c0002t0002g0219a0002c0002t0002g0220others(13): Show | 16 | HG00438.hp2 HG00733.hp2 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.135+10824T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109701376 | ||||||
| chr5:109701386
|
G | T | 2 | a0001c0003t0003g0164a0001c0003t0003g0165 | 2 | HG00741.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.135+10834G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109701386 | ||||||
| chr5:109701398
|
G | C | 1 | a0001c0011t0016g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.135+10846G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109701398 | ||||||
| chr5:109701685
|
T | C | 1 | a0001c0001t0001g0182 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.135+11133T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109701685 | ||||||
| chr5:109701808
|
A | T | 1 | a0001c0003t0012g0168 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.135+11256A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109701808 | ||||||
| chr5:109701829
|
T | C | 83 | a0001c0003t0019g0180a0001c0005t0021g0262a0001c0009t0001g0208others(80): Show | 84 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.135+11277T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109701829 | ||||||
| chr5:109701831
|
G | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(89): Show | 95 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.135+11279G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109701831 | ||||||
| chr5:109701836
|
G | A | 1 | a0002c0002t0002g0273 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.135+11284G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109701836 | ||||||
| chr5:109702247
|
C | A | 2 | a0002c0002t0002g0006a0002c0002t0002g0274 | 3 | NA18947.hp2 NA19000.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.136-11273C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109702247 | ||||||
| chr5:109702268
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.136-11252A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109702268 | ||||||
| chr5:109702276
|
A | T | 42 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(39): Show | 43 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.136-11244A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109702276 | ||||||
| chr5:109702296
|
G | C | 42 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(39): Show | 43 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.136-11224G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109702296 | ||||||
| chr5:109702315
|
T | TTG | 89 | a0001c0003t0003g0147a0001c0003t0003g0148a0001c0003t0003g0149others(86): Show | 91 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.136-11169_136-1116 others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109702315 | |||||
| chr5:109702315
|
T | TTGTG | 15 | a0001c0005t0003g0169a0001c0005t0008g0009a0001c0005t0008g0010others(12): Show | 15 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.136-11171_136-1116 others(8): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109702315 | |||||
| chr5:109702315
|
T | TTGTGTG | 7 | a0001c0004t0004g0034a0001c0005t0003g0054a0001c0005t0008g0011others(4): Show | 7 | HG00099.hp1 HG01109.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-11173_136-1116 others(10): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109702315 | |||||
| chr5:109702315
|
T | TTGTGTGT others(1): Show |
4 | a0001c0004t0013g0214a0001c0004t0013g0282a0001c0005t0010g0015others(1): Show | 4 | HG01192.hp1 HG04228.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-11175_136-1116 others(12): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109702315 | |||||
| chr5:109702315
|
T | TTGTGTGT others(3): Show |
4 | a0001c0005t0010g0019a0002c0002t0002g0212a0002c0002t0002g0283others(1): Show | 4 | HG02257.hp1 HG02970.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-11177_136-1116 others(14): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109702315 | |||||
| chr5:109702315
|
T | TTGTGTGT others(5): Show |
2 | a0001c0004t0013g0049a0001c0005t0010g0020 | 2 | HG02027.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.136-11179_136-1116 others(16): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109702315 | |||||
| chr5:109702315
|
T | TTGTGTGT others(7): Show |
1 | a0001c0006t0006g0172 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.136-11181_136-1116 others(18): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109702315 | |||||
| chr5:109702315
|
TTG | T | 17 | a0001c0001t0001g0081a0001c0001t0001g0108a0001c0001t0001g0109others(14): Show | 17 | HG01109.hp1 HG01168.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.136-11169_136-1116 others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109702315 | |||||
| chr5:109702315
|
TTGTG | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(89): Show | 96 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.136-11171_136-1116 others(8): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109702315 | |||||
| chr5:109702315
|
TTGTGTG | T | 8 | a0001c0004t0004g0041a0001c0004t0004g0042a0001c0004t0004g0043others(5): Show | 8 | HG02258.hp2 HG02717.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-11173_136-1116 others(10): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109702315 | |||||
| chr5:109702315
|
TTGTGTGT others(3): Show |
T | 1 | a0001c0004t0004g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.136-11177_136-1116 others(14): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109702315 | |||||
| chr5:109702353
|
C | G | 1 | a0002c0002t0009g0200 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.136-11167C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109702353 | ||||||
| chr5:109702360
|
T | G | 1 | a0002c0002t0002g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.136-11160T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109702360 | ||||||
| chr5:109702380
|
C | A | 222 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(219): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.136-11140C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109702380 | ||||||
| chr5:109702693
|
A | C | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.136-10827A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109702693 | ||||||
| chr5:109702737
|
T | A | 82 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.136-10783T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109702737 | ||||||
| chr5:109702815
|
C | G | 82 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.136-10705C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109702815 | ||||||
| chr5:109702848
|
T | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.136-10672T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109702848 | ||||||
| chr5:109702928
|
G | A | 83 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0005t0021g0262others(80): Show | 84 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.136-10592G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109702928 | ||||||
| chr5:109703058
|
G | A | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.136-10462G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109703058 | ||||||
| chr5:109703085
|
C | T | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.136-10435C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109703085 | ||||||
| chr5:109703375
|
A | G | 14 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.136-10145A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109703375 | ||||||
| chr5:109703479
|
C | T | 220 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.136-10041C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109703479 | ||||||
| chr5:109703531
|
A | C | 10 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(7): Show | 11 | HG01243.hp1 HG02280.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.136-9989A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109703531 | ||||||
| chr5:109703598
|
T | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(90): Show | 96 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.136-9922T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109703598 | ||||||
| chr5:109703624
|
T | C | 10 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(7): Show | 11 | HG01243.hp1 HG02280.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.136-9896T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109703624 | ||||||
| chr5:109703656
|
A | C | 1 | a0002c0002t0002g0273 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.136-9864A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109703656 | ||||||
| chr5:109703713
|
A | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.136-9807A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109703713 | ||||||
| chr5:109703867
|
A | G | 1 | a0001c0003t0003g0163 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.136-9653A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109703867 | ||||||
| chr5:109703942
|
A | G | 1 | a0002c0002t0025g0263 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.136-9578A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109703942 | ||||||
| chr5:109704072
|
G | T | 14 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.136-9448G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109704072 | ||||||
| chr5:109704188
|
C | A | 1 | a0002c0002t0002g0216 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.136-9332C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109704188 | ||||||
| chr5:109704199
|
C | A | 1 | a0001c0006t0006g0172 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.136-9321C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109704199 | ||||||
| chr5:109704247
|
A | T | 1 | a0001c0001t0001g0076 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.136-9273A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109704247 | ||||||
| chr5:109704265
|
G | A | 82 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.136-9255G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109704265 | ||||||
| chr5:109704415
|
G | A | 14 | a0001c0003t0003g0126a0001c0003t0003g0147a0001c0003t0003g0148others(11): Show | 15 | NA18942.hp2 NA18945.hp2 NA18947.hp1 others(12): Show |
intron_variant | MODIFIER | c.136-9105G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109704415 | ||||||
| chr5:109704541
|
G | A | 83 | a0001c0001t0001g0290a0001c0005t0021g0262a0001c0009t0001g0208others(80): Show | 84 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.136-8979G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109704541 | ||||||
| chr5:109704614
|
T | G | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.136-8906T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109704614 | ||||||
| chr5:109704736
|
C | G | 1 | a0001c0001t0001g0076 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.136-8784C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109704736 | ||||||
| chr5:109704797
|
C | T | 2 | a0001c0001t0001g0107a0002c0002t0002g0272 | 2 | HG01243.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.136-8723C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109704797 | ||||||
| chr5:109704800
|
C | T | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.136-8720C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109704800 | ||||||
| chr5:109704829
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG02145.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.136-8691G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109704829 | ||||||
| chr5:109705051
|
G | A | 222 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(219): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.136-8469G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109705051 | ||||||
| chr5:109705321
|
T | G | 1 | a0001c0001t0001g0108 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.136-8199T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109705321 | ||||||
| chr5:109705394
|
T | G | 20 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(17): Show | 21 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.136-8126T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109705394 | ||||||
| chr5:109705488
|
G | C | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.136-8032G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109705488 | ||||||
| chr5:109705591
|
G | A | 222 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(219): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.136-7929G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109705591 | ||||||
| chr5:109705603
|
A | G | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00438.hp1 HG02074.hp2 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.136-7917A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109705603 | ||||||
| chr5:109705607
|
G | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(88): Show | 94 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.136-7913G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109705607 | ||||||
| chr5:109705645
|
A | G | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.136-7875A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109705645 | ||||||
| chr5:109705734
|
A | T | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.136-7786A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109705734 | ||||||
| chr5:109705841
|
A | G | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.136-7679A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109705841 | ||||||
| chr5:109705890
|
C | T | 3 | a0001c0004t0036g0024a0001c0006t0002g0278a0001c0006t0002g0279 | 3 | HG01891.hp2 HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.136-7630C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109705890 | ||||||
| chr5:109706021
|
G | C | 1 | a0001c0009t0002g0227 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.136-7499G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109706021 | ||||||
| chr5:109706095
|
C | T | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.136-7425C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109706095 | ||||||
| chr5:109706124
|
C | G | 8 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(5): Show | 8 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-7396C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109706124 | ||||||
| chr5:109706143
|
T | C | 42 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(39): Show | 43 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.136-7377T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109706143 | ||||||
| chr5:109706164
|
C | T | 1 | a0009c0015t0001g0075 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.136-7356C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109706164 | ||||||
| chr5:109706316
|
G | T | 14 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.136-7204G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109706316 | ||||||
| chr5:109706389
|
C | G | 1 | a0002c0002t0011g0261 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.136-7131C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109706389 | ||||||
| chr5:109706440
|
C | T | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.136-7080C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109706440 | ||||||
| chr5:109706464
|
A | G | 20 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(17): Show | 21 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.136-7056A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109706464 | ||||||
| chr5:109706529
|
A | G | 1 | a0002c0002t0002g0273 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.136-6991A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109706529 | ||||||
| chr5:109706660
|
A | G | 1 | a0001c0004t0015g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.136-6860A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109706660 | ||||||
| chr5:109706904
|
A | AT | 3 | a0001c0005t0010g0014a0001c0005t0010g0015a0001c0005t0010g0018 | 3 | NA18959.hp1 NA19009.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.136-6613dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109706904 | |||||
| chr5:109706967
|
G | A | 1 | a0001c0011t0016g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.136-6553G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109706967 | ||||||
| chr5:109707170
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.136-6350A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109707170 | ||||||
| chr5:109707224
|
C | G | 1 | a0002c0002t0002g0260 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.136-6296C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109707224 | ||||||
| chr5:109707287
|
T | C | 83 | a0001c0003t0019g0180a0001c0005t0021g0262a0001c0009t0001g0208others(80): Show | 84 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.136-6233T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109707287 | ||||||
| chr5:109707288
|
G | A | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.136-6232G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109707288 | ||||||
| chr5:109707371
|
C | A | 13 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(10): Show | 14 | HG01243.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.136-6149C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109707371 | ||||||
| chr5:109707399
|
T | TC | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.136-6120dupC | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109707399 | |||||
| chr5:109707456
|
A | T | 8 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(5): Show | 8 | HG01255.hp2 HG01361.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-6064A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109707456 | ||||||
| chr5:109707482
|
G | A | 81 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.136-6038G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109707482 | ||||||
| chr5:109707507
|
T | A | 2 | a0002c0002t0009g0007a0002c0002t0009g0215 | 2 | HG00642.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.136-6013T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109707507 | ||||||
| chr5:109707528
|
C | T | 82 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.136-5992C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109707528 | ||||||
| chr5:109707615
|
T | G | 1 | a0001c0003t0003g0127 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.136-5905T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109707615 | ||||||
| chr5:109707746
|
T | A | 3 | a0002c0002t0002g0202a0002c0002t0002g0203a0002c0002t0002g0204 | 3 | NA18957.hp2 NA18969.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.136-5774T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109707746 | ||||||
| chr5:109707949
|
A | T | 3 | a0001c0004t0036g0024a0001c0006t0002g0278a0001c0006t0002g0279 | 3 | HG01891.hp2 HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.136-5571A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109707949 | ||||||
| chr5:109707981
|
G | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(89): Show | 95 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.136-5539G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109707981 | ||||||
| chr5:109708043
|
AAG | A | 82 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.136-5472_136-5471d others(4): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708043 | |||||
| chr5:109708080
|
C | T | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-5440C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109708080 | ||||||
| chr5:109708366
|
T | C | 42 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(39): Show | 43 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.136-5154T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109708366 | ||||||
| chr5:109708433
|
A | T | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.136-5087A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109708433 | ||||||
| chr5:109708464
|
G | C | 1 | a0001c0005t0021g0262 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.136-5056G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109708464 | ||||||
| chr5:109708509
|
G | GAC | 10 | a0001c0003t0003g0163a0001c0003t0003g0207a0001c0003t0007g0177others(7): Show | 10 | HG01106.hp2 HG02895.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.136-4975_136-4974d others(4): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACAC | 7 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0082others(4): Show | 7 | HG01433.hp2 HG01981.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-4977_136-4974d others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACACAC | 56 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(53): Show | 58 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.136-4979_136-4974d others(8): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACACACA others(1): Show |
29 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(26): Show | 29 | HG00639.hp1 HG00642.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.136-4981_136-4974d others(10): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACACACA others(3): Show |
12 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0030g0085others(9): Show | 12 | HG00673.hp2 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.136-4983_136-4974d others(12): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACACACA others(5): Show |
11 | a0001c0004t0004g0001a0001c0004t0004g0043a0001c0004t0004g0044others(8): Show | 13 | HG01109.hp2 HG01192.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.136-4985_136-4974d others(14): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACACACA others(7): Show |
5 | a0001c0004t0004g0042a0001c0004t0015g0040a0001c0006t0002g0279others(2): Show | 5 | HG01891.hp2 HG06807.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-4987_136-4974d others(16): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACACACA others(9): Show |
8 | a0001c0004t0004g0041a0001c0004t0004g0047a0001c0004t0004g0048others(5): Show | 8 | HG02027.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-4989_136-4974d others(18): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACACACA others(11): Show |
13 | a0001c0005t0008g0017a0001c0005t0010g0015a0001c0005t0010g0018others(10): Show | 13 | HG00438.hp2 HG01081.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.136-4991_136-4974d others(20): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACACACA others(13): Show |
11 | a0001c0001t0001g0057a0001c0005t0008g0010a0001c0005t0008g0012others(8): Show | 12 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.136-4993_136-4974d others(22): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACACACA others(15): Show |
14 | a0001c0005t0008g0009a0001c0009t0002g0227a0001c0009t0028g0008others(11): Show | 14 | HG02027.hp2 HG02129.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.136-4995_136-4974d others(24): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACACACA others(17): Show |
7 | a0001c0005t0003g0169a0002c0002t0002g0202a0002c0002t0002g0219others(4): Show | 7 | HG02155.hp1 HG02257.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-4997_136-4974d others(26): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACACACA others(19): Show |
6 | a0001c0009t0001g0208a0001c0011t0016g0026a0002c0002t0002g0226others(3): Show | 6 | HG00099.hp2 HG02040.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-4999_136-4974d others(28): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACACACA others(21): Show |
11 | a0001c0011t0016g0025a0002c0002t0002g0212a0002c0002t0002g0230others(8): Show | 11 | HG02132.hp2 HG02135.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-5001_136-4974d others(30): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACACACA others(23): Show |
8 | a0002c0002t0002g0178a0002c0002t0002g0229a0002c0002t0002g0241others(5): Show | 8 | HG00733.hp2 HG01981.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-5003_136-4974d others(32): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACACACA others(25): Show |
7 | a0001c0005t0008g0011a0001c0005t0021g0262a0002c0002t0002g0204others(4): Show | 7 | HG00099.hp1 HG02056.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-5005_136-4974d others(34): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACACACA others(27): Show |
7 | a0001c0001t0001g0290a0002c0002t0002g0189a0002c0002t0002g0205others(4): Show | 7 | HG00735.hp1 HG01934.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-5007_136-4974d others(36): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACACACA others(29): Show |
3 | a0002c0002t0002g0235a0002c0002t0002g0236a0002c0002t0025g0263 | 3 | HG00609.hp2 HG01978.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.136-5009_136-4974d others(38): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACACACA others(33): Show |
1 | a0002c0002t0002g0269 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.136-4974_136-4973i others(42): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GACAGACA others(27): Show |
1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-5008_136-5007i others(36): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708509
|
G | GAGACACA others(5): Show |
1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.136-5010_136-5009i others(14): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708509 | |||||
| chr5:109708545
|
CAT | C | 3 | a0001c0003t0003g0146a0001c0003t0003g0170a0001c0003t0003g0171 | 3 | HG00735.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.136-4974_136-4973d others(4): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109708545 | ||||||
| chr5:109708547
|
T | C | 112 | a0001c0001t0001g0290a0001c0003t0003g0027a0001c0004t0004g0001others(109): Show | 114 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.136-4973T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109708547 | ||||||
| chr5:109708569
|
AT | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.136-4949delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109708569 | |||||
| chr5:109708608
|
T | C | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.136-4912T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109708608 | ||||||
| chr5:109708707
|
T | A | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.136-4813T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109708707 | ||||||
| chr5:109708767
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.136-4753G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109708767 | ||||||
| chr5:109708789
|
A | G | 3 | a0001c0003t0003g0143a0001c0003t0003g0145a0001c0003t0018g0144 | 3 | HG00140.hp2 HG01069.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.136-4731A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109708789 | ||||||
| chr5:109708857
|
C | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(89): Show | 95 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.136-4663C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109708857 | ||||||
| chr5:109708991
|
A | G | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.136-4529A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109708991 | ||||||
| chr5:109709079
|
G | A | 1 | a0001c0013t0003g0155 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.136-4441G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109709079 | ||||||
| chr5:109709093
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.136-4427A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109709093 | ||||||
| chr5:109709173
|
A | AG | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(220): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.136-4346dupG | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109709173 | |||||
| chr5:109709207
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.136-4313A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109709207 | ||||||
| chr5:109709282
|
A | C | 1 | a0001c0011t0016g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.136-4238A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109709282 | ||||||
| chr5:109709648
|
G | T | 1 | a0001c0001t0001g0182 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.136-3872G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109709648 | ||||||
| chr5:109709986
|
C | T | 1 | a0001c0003t0012g0168 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.136-3534C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109709986 | ||||||
| chr5:109710318
|
A | G | 4 | a0001c0003t0003g0160a0001c0003t0003g0161a0001c0003t0003g0162others(1): Show | 4 | HG00597.hp1 HG02056.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-3202A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109710318 | ||||||
| chr5:109710478
|
A | G | 1 | a0002c0002t0002g0240 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.136-3042A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109710478 | ||||||
| chr5:109710507
|
G | GT | 3 | a0002c0002t0002g0178a0002c0002t0002g0229a0002c0002t0002g0244 | 3 | HG02074.hp1 HG02300.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.136-3012dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109710507 | |||||
| chr5:109710509
|
A | T | 83 | a0001c0001t0001g0290a0001c0005t0021g0262a0001c0009t0001g0208others(80): Show | 84 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.136-3011A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109710509 | ||||||
| chr5:109710510
|
T | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.136-3010T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109710510 | ||||||
| chr5:109710541
|
A | G | 1 | a0002c0002t0011g0268 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.136-2979A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109710541 | ||||||
| chr5:109710543
|
C | T | 1 | a0001c0004t0004g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.136-2977C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109710543 | ||||||
| chr5:109710548
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.136-2972A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109710548 | ||||||
| chr5:109710672
|
T | C | 42 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(39): Show | 43 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.136-2848T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109710672 | ||||||
| chr5:109710696
|
A | AT | 20 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(17): Show | 21 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.136-2813dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109710696 | |||||
| chr5:109710753
|
C | T | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.136-2767C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109710753 | ||||||
| chr5:109710879
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.136-2641G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109710879 | ||||||
| chr5:109710900
|
G | T | 1 | a0002c0002t0002g0178 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.136-2620G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109710900 | ||||||
| chr5:109710941
|
C | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-2579C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109710941 | ||||||
| chr5:109710947
|
C | T | 2 | a0002c0002t0009g0217a0002c0002t0034g0218 | 2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.136-2573C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109710947 | ||||||
| chr5:109711292
|
G | T | 11 | a0001c0005t0008g0009a0001c0005t0008g0010a0001c0005t0008g0011others(8): Show | 11 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.136-2228G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109711292 | ||||||
| chr5:109711307
|
G | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.136-2213G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109711307 | ||||||
| chr5:109711448
|
C | CTG | 220 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.136-2070_136-2069d others(4): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109711448 | |||||
| chr5:109711546
|
A | T | 6 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(3): Show | 6 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-1974A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109711546 | ||||||
| chr5:109711601
|
G | A | 4 | a0001c0004t0036g0024a0001c0006t0002g0278a0001c0006t0002g0279others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-1919G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109711601 | ||||||
| chr5:109711608
|
C | T | 78 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(75): Show | 79 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.136-1912C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109711608 | ||||||
| chr5:109711638
|
A | G | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-1882A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109711638 | ||||||
| chr5:109711737
|
C | A | 34 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(31): Show | 35 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.136-1783C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109711737 | ||||||
| chr5:109711911
|
AG | A | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(223): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.136-1605delG | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109711911 | |||||
| chr5:109712011
|
G | A | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(220): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.136-1509G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109712011 | ||||||
| chr5:109712032
|
C | T | 1 | a0001c0003t0003g0159 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.136-1488C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109712032 | ||||||
| chr5:109712095
|
C | CT | 111 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(108): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.136-1410dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109712095 | |||||
| chr5:109712095
|
CT | C | 9 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 9 | HG01255.hp2 HG01361.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-1410delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109712095 | |||||
| chr5:109712110
|
T | A | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-1410T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109712110 | ||||||
| chr5:109712432
|
C | T | 34 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(31): Show | 35 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.136-1088C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109712432 | ||||||
| chr5:109712503
|
A | G | 21 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(18): Show | 21 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.136-1017A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109712503 | ||||||
| chr5:109712647
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.136-873A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109712647 | ||||||
| chr5:109712772
|
G | A | 1 | a0002c0002t0002g0240 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.136-748G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109712772 | ||||||
| chr5:109713175
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.136-345G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109713175 | ||||||
| chr5:109713285
|
G | A | 13 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(10): Show | 14 | HG01243.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.136-235G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109713285 | ||||||
| chr5:109713412
|
G | T | 1 | a0002c0002t0002g0272 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.136-108G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109713412 | ||||||
| chr5:109713414
|
G | T | 1 | a0001c0003t0007g0177 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.136-106G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109713414 | ||||||
| chr5:109713444
|
T | TA | 14 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.136-65dupA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 109713444 | |||||
| chr5:109713477
|
A | G | 37 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(34): Show | 38 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.136-43A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | chr5 | 109713477 | ||||||
| chr5:109713806
|
C | CT | 43 | a0001c0001t0001g0039a0001c0001t0001g0056a0001c0001t0001g0083others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.390+45dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 109713806 | |||||
| chr5:109713806
|
C | G | 79 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(76): Show | 80 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.390+32C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109713806 | ||||||
| chr5:109713806
|
C | T | 2 | a0002c0002t0002g0178a0002c0002t0002g0204 | 2 | HG02300.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.390+32C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109713806 | ||||||
| chr5:109713817
|
T | G | 1 | a0001c0001t0001g0060 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.390+43T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109713817 | ||||||
| chr5:109713836
|
G | A | 1 | a0006c0012t0001g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.390+62G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109713836 | ||||||
| chr5:109713842
|
A | T | 1 | a0001c0001t0001g0060 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.390+68A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109713842 | ||||||
| chr5:109713986
|
A | G | 1 | a0001c0003t0003g0162 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.390+212A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109713986 | ||||||
| chr5:109713998
|
C | T | 6 | a0002c0002t0002g0189a0002c0002t0002g0236a0002c0002t0002g0239others(3): Show | 6 | HG00099.hp2 HG01934.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+224C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109713998 | ||||||
| chr5:109714005
|
A | G | 10 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(7): Show | 10 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+231A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109714005 | ||||||
| chr5:109714132
|
A | G | 1 | a0002c0002t0002g0229 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.390+358A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109714132 | ||||||
| chr5:109714159
|
G | T | 1 | a0001c0003t0019g0180 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.390+385G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109714159 | ||||||
| chr5:109714163
|
A | C | 13 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(10): Show | 13 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.390+389A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109714163 | ||||||
| chr5:109714176
|
AC | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.390+403delC | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109714176 | ||||||
| chr5:109714177
|
C | CT | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(90): Show | 96 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.390+417dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 109714177 | |||||
| chr5:109714177
|
C | CTT | 8 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(5): Show | 8 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.390+416_390+417dup others(2): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 109714177 | |||||
| chr5:109714265
|
G | A | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.390+491G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109714265 | ||||||
| chr5:109714307
|
T | G | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(223): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.390+533T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109714307 | ||||||
| chr5:109714412
|
T | C | 82 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.390+638T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109714412 | ||||||
| chr5:109714692
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.390+918A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109714692 | ||||||
| chr5:109714733
|
C | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(91): Show | 97 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.390+959C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109714733 | ||||||
| chr5:109714786
|
A | C | 1 | a0003c0007t0001g0198 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.390+1012A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109714786 | ||||||
| chr5:109714859
|
C | G | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.390+1085C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109714859 | ||||||
| chr5:109714889
|
T | C | 1 | a0001c0006t0002g0279 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.390+1115T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109714889 | ||||||
| chr5:109714989
|
C | CA | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(98): Show | 104 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.391-1113dupA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 109714989 | |||||
| chr5:109715006
|
A | C | 1 | a0004c0008t0014g0023 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.391-1114A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109715006 | ||||||
| chr5:109715019
|
G | T | 1 | a0002c0002t0002g0202 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.391-1101G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109715019 | ||||||
| chr5:109715122
|
A | G | 1 | a0002c0002t0027g0234 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.391-998A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109715122 | ||||||
| chr5:109715200
|
T | C | 34 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(31): Show | 35 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.391-920T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109715200 | ||||||
| chr5:109715291
|
T | TTAAATTT others(314): Show |
3 | a0002c0002t0002g0219a0002c0002t0002g0221a0002c0002t0002g0225 | 3 | NA18942.hp1 NA18945.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.391-817_391-816ins others(321): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 109715291 | |||||
| chr5:109715291
|
T | TTAAATTT others(315): Show |
1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.391-817_391-816ins others(322): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 109715291 | |||||
| chr5:109715291
|
T | TTAAATTT others(315): Show |
73 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(70): Show | 74 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.391-817_391-816ins others(322): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 109715291 | |||||
| chr5:109715291
|
T | TTAAATTT others(315): Show |
1 | a0002c0002t0009g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.391-817_391-816ins others(322): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 109715291 | |||||
| chr5:109715291
|
T | TTAAATTT others(315): Show |
2 | a0002c0002t0002g0236a0002c0002t0002g0239 | 2 | HG01934.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.391-817_391-816ins others(322): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 109715291 | |||||
| chr5:109715291
|
T | TTAAATTT others(316): Show |
2 | a0002c0002t0002g0232a0002c0002t0002g0274 | 2 | NA18982.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.391-817_391-816ins others(323): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 109715291 | |||||
| chr5:109715362
|
A | T | 1 | a0001c0003t0012g0168 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.391-758A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109715362 | ||||||
| chr5:109715445
|
G | A | 1 | a0002c0002t0002g0244 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.391-675G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109715445 | ||||||
| chr5:109715526
|
C | G | 1 | a0001c0004t0029g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.391-594C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109715526 | ||||||
| chr5:109715554
|
A | AT | 15 | a0001c0003t0003g0126a0001c0003t0003g0147a0001c0003t0003g0148others(12): Show | 16 | HG03704.hp2 NA18942.hp2 NA18945.hp2 others(13): Show |
intron_variant | MODIFIER | c.391-561dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 109715554 | |||||
| chr5:109715637
|
C | A | 220 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.391-483C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109715637 | ||||||
| chr5:109715718
|
A | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(220): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.391-402A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109715718 | ||||||
| chr5:109716009
|
A | G | 1 | a0001c0003t0003g0127 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.391-111A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 2/21 | chr5 | 109716009 | ||||||
| chr5:109716286
|
G | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0005g0111 | 3 | HG01123.hp2 HG01346.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.535+22G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109716286 | ||||||
| chr5:109716385
|
A | G | 82 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.535+121A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109716385 | ||||||
| chr5:109716406
|
G | C | 1 | a0001c0004t0004g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.535+142G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109716406 | ||||||
| chr5:109716502
|
G | C | 1 | a0002c0002t0002g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.535+238G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109716502 | ||||||
| chr5:109716660
|
A | G | 8 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(5): Show | 8 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.535+396A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109716660 | ||||||
| chr5:109716770
|
G | C | 1 | a0003c0007t0001g0198 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.535+506G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109716770 | ||||||
| chr5:109716909
|
G | C | 10 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(7): Show | 11 | HG01243.hp1 HG02280.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.535+645G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109716909 | ||||||
| chr5:109716958
|
G | T | 82 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.535+694G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109716958 | ||||||
| chr5:109716982
|
G | A | 1 | a0002c0002t0002g0289 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.535+718G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109716982 | ||||||
| chr5:109717063
|
A | AT | 31 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.535+810dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr5 | 109717063 | |||||
| chr5:109717146
|
C | T | 42 | a0001c0005t0021g0262a0002c0002t0002g0006a0002c0002t0002g0189others(39): Show | 43 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.535+882C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109717146 | ||||||
| chr5:109717224
|
T | C | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.535+960T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109717224 | ||||||
| chr5:109717335
|
A | G | 1 | a0002c0002t0002g0236 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.535+1071A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109717335 | ||||||
| chr5:109717432
|
A | G | 82 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.535+1168A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109717432 | ||||||
| chr5:109717592
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.535+1328T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109717592 | ||||||
| chr5:109717634
|
A | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(98): Show | 104 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.535+1370A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109717634 | ||||||
| chr5:109717703
|
A | G | 4 | a0001c0003t0003g0124a0001c0003t0003g0125a0001c0003t0003g0142others(1): Show | 4 | HG01109.hp1 HG01175.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.535+1439A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109717703 | ||||||
| chr5:109717759
|
T | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(88): Show | 94 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.535+1495T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109717759 | ||||||
| chr5:109717779
|
T | A | 1 | a0002c0002t0002g0242 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.535+1515T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109717779 | ||||||
| chr5:109717780
|
A | T | 1 | a0002c0002t0002g0242 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.535+1516A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109717780 | ||||||
| chr5:109717931
|
C | T | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.535+1667C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109717931 | ||||||
| chr5:109718044
|
C | A | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.535+1780C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109718044 | ||||||
| chr5:109718086
|
T | C | 3 | a0001c0004t0036g0024a0001c0006t0002g0278a0001c0006t0002g0279 | 3 | HG01891.hp2 HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.535+1822T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109718086 | ||||||
| chr5:109718193
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.535+1929A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109718193 | ||||||
| chr5:109718226
|
G | C | 1 | a0001c0001t0005g0077 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.535+1962G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109718226 | ||||||
| chr5:109718542
|
C | T | 13 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(10): Show | 14 | HG01243.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.535+2278C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109718542 | ||||||
| chr5:109718614
|
A | G | 1 | a0001c0001t0005g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.535+2350A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109718614 | ||||||
| chr5:109718618
|
C | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.535+2354C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109718618 | ||||||
| chr5:109718632
|
C | A | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.535+2368C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109718632 | ||||||
| chr5:109718665
|
A | C | 1 | a0001c0001t0005g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.535+2401A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109718665 | ||||||
| chr5:109718686
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.535+2422G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109718686 | ||||||
| chr5:109718831
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.535+2567G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109718831 | ||||||
| chr5:109718848
|
G | A | 1 | a0001c0004t0004g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.535+2584G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109718848 | ||||||
| chr5:109718923
|
C | T | 3 | a0002c0002t0002g0219a0002c0002t0002g0221a0002c0002t0002g0225 | 3 | NA18942.hp1 NA18945.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.535+2659C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109718923 | ||||||
| chr5:109718973
|
TTCTTAAA others(24): Show |
T | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(89): Show | 95 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.535+2714_535+2744d others(33): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr5 | 109718973 | |||||
| chr5:109718977
|
T | TA | 44 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(41): Show | 45 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.535+2726dupA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr5 | 109718977 | |||||
| chr5:109719100
|
A | G | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.535+2836A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109719100 | ||||||
| chr5:109719154
|
G | A | 42 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(39): Show | 43 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.535+2890G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109719154 | ||||||
| chr5:109719233
|
C | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.535+2969C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109719233 | ||||||
| chr5:109719303
|
T | C | 1 | a0001c0005t0010g0014 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+3039T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109719303 | ||||||
| chr5:109719379
|
A | T | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.535+3115A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109719379 | ||||||
| chr5:109719488
|
G | C | 130 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(127): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.535+3224G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109719488 | ||||||
| chr5:109719550
|
A | G | 14 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.535+3286A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109719550 | ||||||
| chr5:109719648
|
C | T | 1 | a0009c0015t0001g0075 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.535+3384C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109719648 | ||||||
| chr5:109720077
|
A | G | 1 | a0008c0019t0002g0250 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.535+3813A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109720077 | ||||||
| chr5:109720138
|
C | G | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.535+3874C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109720138 | ||||||
| chr5:109720172
|
T | C | 20 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(17): Show | 21 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.535+3908T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109720172 | ||||||
| chr5:109720179
|
A | C | 6 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(3): Show | 6 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.535+3915A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109720179 | ||||||
| chr5:109720227
|
A | G | 1 | a0001c0004t0015g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.535+3963A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109720227 | ||||||
| chr5:109720354
|
C | T | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.535+4090C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109720354 | ||||||
| chr5:109720867
|
G | A | 22 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.535+4603G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109720867 | ||||||
| chr5:109720941
|
T | C | 42 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(39): Show | 43 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.535+4677T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109720941 | ||||||
| chr5:109721078
|
A | AT | 20 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(17): Show | 21 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.535+4820dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr5 | 109721078 | |||||
| chr5:109721127
|
G | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(89): Show | 95 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.535+4863G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109721127 | ||||||
| chr5:109721140
|
A | G | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.535+4876A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109721140 | ||||||
| chr5:109721183
|
T | C | 1 | a0003c0007t0001g0198 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.535+4919T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109721183 | ||||||
| chr5:109721592
|
T | C | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.535+5328T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109721592 | ||||||
| chr5:109721837
|
A | G | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.535+5573A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109721837 | ||||||
| chr5:109722383
|
G | A | 2 | a0002c0002t0009g0217a0002c0002t0034g0218 | 2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.535+6119G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109722383 | ||||||
| chr5:109722393
|
C | T | 13 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(10): Show | 13 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.535+6129C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109722393 | ||||||
| chr5:109722483
|
C | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.535+6219C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109722483 | ||||||
| chr5:109722522
|
C | A | 1 | a0001c0006t0006g0038 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.535+6258C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109722522 | ||||||
| chr5:109722529
|
C | G | 1 | a0001c0005t0021g0262 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.535+6265C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109722529 | ||||||
| chr5:109722560
|
A | G | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.535+6296A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109722560 | ||||||
| chr5:109722631
|
G | A | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.535+6367G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109722631 | ||||||
| chr5:109722637
|
A | T | 1 | a0001c0003t0003g0162 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.535+6373A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109722637 | ||||||
| chr5:109722661
|
C | T | 1 | a0001c0004t0004g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.535+6397C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109722661 | ||||||
| chr5:109722705
|
C | T | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.535+6441C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109722705 | ||||||
| chr5:109722706
|
G | A | 4 | a0003c0007t0001g0194a0003c0007t0001g0195a0003c0007t0001g0196others(1): Show | 4 | HG00609.hp1 HG00673.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.535+6442G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109722706 | ||||||
| chr5:109722797
|
C | T | 1 | a0001c0004t0004g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.535+6533C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109722797 | ||||||
| chr5:109722893
|
A | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(87): Show | 93 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.536-6449A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109722893 | ||||||
| chr5:109722894
|
G | A | 1 | a0001c0003t0003g0129 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.536-6448G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109722894 | ||||||
| chr5:109722982
|
G | A | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(215): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.536-6360G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109722982 | ||||||
| chr5:109723034
|
G | T | 1 | a0001c0001t0001g0055 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.536-6308G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109723034 | ||||||
| chr5:109723110
|
G | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.536-6232G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109723110 | ||||||
| chr5:109723189
|
A | C | 1 | a0001c0006t0006g0172 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.536-6153A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109723189 | ||||||
| chr5:109723437
|
T | A | 1 | a0001c0004t0029g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.536-5905T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109723437 | ||||||
| chr5:109723447
|
G | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.536-5895G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109723447 | ||||||
| chr5:109723507
|
C | A | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.536-5835C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109723507 | ||||||
| chr5:109723574
|
A | G | 1 | a0001c0003t0003g0145 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.536-5768A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109723574 | ||||||
| chr5:109723624
|
C | T | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.536-5718C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109723624 | ||||||
| chr5:109724132
|
T | A | 82 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.536-5210T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109724132 | ||||||
| chr5:109724251
|
A | G | 1 | a0002c0002t0025g0263 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.536-5091A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109724251 | ||||||
| chr5:109724447
|
T | G | 14 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.536-4895T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109724447 | ||||||
| chr5:109724664
|
TA | T | 4 | a0001c0006t0006g0285a0001c0006t0006g0286a0001c0006t0006g0287others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.536-4672delA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr5 | 109724664 | |||||
| chr5:109724672
|
C | T | 7 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(4): Show | 7 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.536-4670C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109724672 | ||||||
| chr5:109724817
|
A | G | 222 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(219): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.536-4525A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109724817 | ||||||
| chr5:109724885
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.536-4457A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109724885 | ||||||
| chr5:109724972
|
A | G | 2 | a0001c0003t0007g0140a0001c0003t0007g0141 | 2 | HG01168.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.536-4370A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109724972 | ||||||
| chr5:109724983
|
C | T | 1 | a0002c0002t0002g0273 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.536-4359C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109724983 | ||||||
| chr5:109724994
|
A | G | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.536-4348A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109724994 | ||||||
| chr5:109725081
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.536-4261G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109725081 | ||||||
| chr5:109725104
|
A | T | 222 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(219): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.536-4238A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109725104 | ||||||
| chr5:109725125
|
G | T | 1 | a0001c0005t0010g0015 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.536-4217G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109725125 | ||||||
| chr5:109725199
|
C | T | 2 | a0006c0012t0001g0028a0006c0012t0001g0029 | 2 | HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.536-4143C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109725199 | ||||||
| chr5:109725812
|
A | C | 2 | a0001c0003t0003g0124a0001c0003t0003g0125 | 2 | HG01109.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.536-3530A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109725812 | ||||||
| chr5:109725883
|
A | G | 45 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(42): Show | 46 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.536-3459A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109725883 | ||||||
| chr5:109725917
|
A | G | 3 | a0001c0001t0001g0056a0001c0004t0004g0041a0001c0004t0004g0042 | 3 | HG02965.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.536-3425A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109725917 | ||||||
| chr5:109726259
|
A | G | 82 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.536-3083A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109726259 | ||||||
| chr5:109726276
|
C | T | 1 | a0001c0003t0003g0165 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.536-3066C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109726276 | ||||||
| chr5:109726344
|
A | G | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(224): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.536-2998A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109726344 | ||||||
| chr5:109726397
|
A | G | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.536-2945A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109726397 | ||||||
| chr5:109726410
|
G | A | 2 | a0001c0005t0003g0054a0001c0005t0003g0169 | 2 | HG01109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.536-2932G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109726410 | ||||||
| chr5:109726492
|
C | T | 3 | a0001c0001t0001g0060a0001c0011t0016g0025a0001c0011t0016g0026 | 3 | HG02055.hp1 HG03139.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.536-2850C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109726492 | ||||||
| chr5:109726724
|
T | C | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(221): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.536-2618T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109726724 | ||||||
| chr5:109726797
|
G | A | 1 | a0002c0002t0002g0266 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.536-2545G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109726797 | ||||||
| chr5:109726869
|
G | A | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.536-2473G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109726869 | ||||||
| chr5:109726906
|
T | G | 4 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.536-2436T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109726906 | ||||||
| chr5:109726925
|
C | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(89): Show | 95 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.536-2417C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109726925 | ||||||
| chr5:109727288
|
G | A | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.536-2054G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109727288 | ||||||
| chr5:109727424
|
C | T | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.536-1918C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109727424 | ||||||
| chr5:109727513
|
C | A | 30 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(27): Show | 31 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.536-1829C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109727513 | ||||||
| chr5:109727814
|
T | A | 4 | a0001c0001t0001g0086a0001c0004t0013g0049a0001c0004t0013g0214others(1): Show | 4 | HG00639.hp1 HG01192.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.536-1528T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109727814 | ||||||
| chr5:109727893
|
T | G | 1 | a0002c0002t0002g0205 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.536-1449T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109727893 | ||||||
| chr5:109727942
|
GAC | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.536-1396_536-1395d others(4): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr5 | 109727942 | |||||
| chr5:109728119
|
T | C | 6 | a0001c0006t0006g0038a0001c0006t0006g0172a0001c0006t0006g0285others(3): Show | 6 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.536-1223T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109728119 | ||||||
| chr5:109728407
|
G | A | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.536-935G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109728407 | ||||||
| chr5:109728539
|
TG | T | 20 | a0001c0004t0004g0001a0001c0004t0004g0043a0001c0004t0004g0044others(17): Show | 21 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.536-802delG | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109728539 | ||||||
| chr5:109728598
|
T | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(116): Show | 122 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.536-744T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109728598 | ||||||
| chr5:109728653
|
C | T | 2 | a0001c0005t0003g0054a0001c0005t0003g0169 | 2 | HG01109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.536-689C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109728653 | ||||||
| chr5:109728720
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.536-622A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109728720 | ||||||
| chr5:109728990
|
T | G | 1 | a0001c0001t0001g0087 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.536-352T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109728990 | ||||||
| chr5:109729039
|
AG | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(115): Show | 121 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.536-302delG | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109729039 | ||||||
| chr5:109729122
|
G | A | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.536-220G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109729122 | ||||||
| chr5:109729176
|
A | G | 4 | a0001c0003t0003g0151a0001c0003t0003g0152a0001c0003t0003g0154others(1): Show | 4 | NA18945.hp2 NA18965.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.536-166A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109729176 | ||||||
| chr5:109729272
|
A | G | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.536-70A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109729272 | ||||||
| chr5:109729308
|
T | A | 8 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0006g0038others(5): Show | 8 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.536-34T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 3/21 | chr5 | 109729308 | ||||||
| chr5:109729559
|
T | C | 1 | a0001c0003t0003g0143 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.707+46T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109729559 | ||||||
| chr5:109729590
|
A | T | 2 | a0002c0002t0002g0271a0002c0002t0002g0272 | 2 | NA18949.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.707+77A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109729590 | ||||||
| chr5:109729692
|
C | G | 1 | a0001c0003t0003g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.707+179C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109729692 | ||||||
| chr5:109729885
|
A | G | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(224): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.707+372A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109729885 | ||||||
| chr5:109729893
|
C | G | 1 | a0001c0003t0007g0141 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.707+380C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109729893 | ||||||
| chr5:109729907
|
C | T | 6 | a0001c0003t0003g0137a0001c0003t0003g0138a0001c0003t0003g0146others(3): Show | 6 | HG00735.hp2 HG01256.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.707+394C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109729907 | ||||||
| chr5:109729990
|
T | C | 1 | a0002c0002t0011g0261 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.707+477T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109729990 | ||||||
| chr5:109730007
|
T | C | 32 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(29): Show | 33 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.707+494T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109730007 | ||||||
| chr5:109730050
|
T | G | 82 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.707+537T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109730050 | ||||||
| chr5:109730050
|
TG | T | 6 | a0001c0006t0006g0038a0001c0006t0006g0172a0001c0006t0006g0285others(3): Show | 6 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.707+539delG | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109730050 | |||||
| chr5:109730081
|
A | G | 81 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.707+568A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109730081 | ||||||
| chr5:109730168
|
C | G | 1 | a0002c0002t0002g0206 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.707+655C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109730168 | ||||||
| chr5:109730495
|
CAAAT | C | 7 | a0002c0002t0002g0006a0002c0002t0002g0206a0002c0002t0002g0240others(4): Show | 8 | HG00609.hp2 HG00673.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.707+988_707+991del others(4): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109730495 | |||||
| chr5:109730529
|
T | C | 1 | a0002c0002t0002g0260 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.707+1016T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109730529 | ||||||
| chr5:109730557
|
G | A | 1 | a0001c0005t0008g0010 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.707+1044G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109730557 | ||||||
| chr5:109730560
|
T | TA | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(140): Show | 147 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.707+1055dupA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109730560 | |||||
| chr5:109730576
|
C | T | 6 | a0001c0006t0006g0038a0001c0006t0006g0172a0001c0006t0006g0285others(3): Show | 6 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.707+1063C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109730576 | ||||||
| chr5:109730748
|
G | A | 1 | a0001c0003t0003g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.707+1235G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109730748 | ||||||
| chr5:109730763
|
A | C | 85 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282others(82): Show | 86 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.707+1250A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109730763 | ||||||
| chr5:109730794
|
C | G | 1 | a0001c0001t0005g0058 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.707+1281C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109730794 | ||||||
| chr5:109730878
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.707+1365G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109730878 | ||||||
| chr5:109730879
|
C | A | 28 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(25): Show | 29 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.707+1366C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109730879 | ||||||
| chr5:109730885
|
T | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(224): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.707+1372T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109730885 | ||||||
| chr5:109731029
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.707+1516G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731029 | ||||||
| chr5:109731040
|
T | G | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(221): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.707+1527T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731040 | ||||||
| chr5:109731069
|
T | C | 1 | a0002c0002t0002g0243 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.707+1556T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731069 | ||||||
| chr5:109731101
|
T | C | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.707+1588T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731101 | ||||||
| chr5:109731218
|
T | C | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(221): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.707+1705T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731218 | ||||||
| chr5:109731374
|
ATTATAC | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(104): Show | 110 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.707+1864_707+1869d others(8): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109731374 | |||||
| chr5:109731415
|
G | A | 1 | a0001c0003t0003g0027 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.707+1902G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731415 | ||||||
| chr5:109731483
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.707+1970G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731483 | ||||||
| chr5:109731516
|
C | T | 1 | a0001c0003t0003g0127 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.707+2003C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731516 | ||||||
| chr5:109731518
|
A | C | 289 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.707+2005A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731518 | ||||||
| chr5:109731520
|
C | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.707+2007C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731520 | ||||||
| chr5:109731623
|
G | T | 82 | a0001c0005t0021g0262a0001c0009t0001g0208a0001c0009t0002g0227others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.707+2110G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731623 | ||||||
| chr5:109731696
|
C | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(87): Show | 93 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.707+2183C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731696 | ||||||
| chr5:109731697
|
T | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(87): Show | 93 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.707+2184T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731697 | ||||||
| chr5:109731715
|
T | G | 6 | a0001c0003t0003g0156a0001c0003t0003g0157a0001c0003t0003g0158others(3): Show | 6 | HG01192.hp2 HG01433.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.707+2202T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731715 | ||||||
| chr5:109731750
|
G | C | 1 | a0007c0014t0002g0193 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.707+2237G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731750 | ||||||
| chr5:109731757
|
A | G | 1 | a0002c0002t0002g0230 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.707+2244A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731757 | ||||||
| chr5:109731806
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(104): Show | 110 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.707+2293G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731806 | ||||||
| chr5:109731811
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(87): Show | 93 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.707+2298G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731811 | ||||||
| chr5:109731824
|
A | G | 220 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.707+2311A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731824 | ||||||
| chr5:109731882
|
T | C | 1 | a0001c0005t0035g0013 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.707+2369T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731882 | ||||||
| chr5:109731949
|
G | A | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(221): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.707+2436G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109731949 | ||||||
| chr5:109732003
|
C | T | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.707+2490C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109732003 | ||||||
| chr5:109732021
|
C | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(87): Show | 93 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.707+2508C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109732021 | ||||||
| chr5:109732159
|
T | A | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.707+2646T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109732159 | ||||||
| chr5:109732188
|
T | C | 2 | a0001c0004t0004g0001a0001c0004t0004g0044 | 3 | HG02280.hp1 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.707+2675T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109732188 | ||||||
| chr5:109732303
|
T | G | 3 | a0001c0003t0003g0137a0001c0003t0003g0138a0001c0003t0003g0192 | 3 | HG01256.hp1 HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.707+2790T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109732303 | ||||||
| chr5:109732361
|
A | G | 10 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0005g0281others(7): Show | 10 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.707+2848A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109732361 | ||||||
| chr5:109732530
|
A | G | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.707+3017A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109732530 | ||||||
| chr5:109732539
|
A | G | 2 | a0002c0002t0002g0232a0002c0002t0002g0280 | 2 | HG01123.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.707+3026A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109732539 | ||||||
| chr5:109732575
|
G | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(105): Show | 111 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.707+3062G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109732575 | ||||||
| chr5:109732577
|
T | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(105): Show | 111 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.707+3064T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109732577 | ||||||
| chr5:109732672
|
C | T | 4 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282others(1): Show | 4 | HG01192.hp1 HG03017.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.707+3159C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109732672 | ||||||
| chr5:109732718
|
G | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(105): Show | 111 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.707+3205G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109732718 | ||||||
| chr5:109732742
|
C | A | 110 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(107): Show | 112 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.707+3229C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109732742 | ||||||
| chr5:109732747
|
G | A | 6 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 6 | HG02647.hp1 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.707+3234G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109732747 | ||||||
| chr5:109732752
|
T | G | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.707+3239T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109732752 | ||||||
| chr5:109732798
|
A | C | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.707+3285A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109732798 | ||||||
| chr5:109733101
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.707+3588A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733101 | ||||||
| chr5:109733124
|
A | C | 1 | a0002c0002t0011g0179 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.707+3611A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733124 | ||||||
| chr5:109733169
|
G | C | 23 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(20): Show | 23 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.707+3656G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733169 | ||||||
| chr5:109733179
|
T | A | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.707+3666T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733179 | ||||||
| chr5:109733205
|
G | C | 1 | a0001c0004t0004g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.707+3692G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733205 | ||||||
| chr5:109733231
|
G | A | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.707+3718G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733231 | ||||||
| chr5:109733269
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.707+3756C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733269 | ||||||
| chr5:109733300
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.707+3787G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733300 | ||||||
| chr5:109733369
|
A | G | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.707+3856A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733369 | ||||||
| chr5:109733435
|
T | G | 1 | a0001c0003t0003g0207 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.707+3922T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733435 | ||||||
| chr5:109733556
|
G | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.707+4043G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733556 | ||||||
| chr5:109733560
|
T | A | 31 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(28): Show | 32 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.707+4047T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733560 | ||||||
| chr5:109733573
|
T | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0055a0001c0001t0001g0082others(3): Show | 7 | HG00639.hp1 HG01256.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.707+4060T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733573 | ||||||
| chr5:109733575
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0055a0001c0001t0001g0082others(3): Show | 7 | HG00639.hp1 HG01256.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.707+4062T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733575 | ||||||
| chr5:109733580
|
G | T | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.707+4067G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733580 | ||||||
| chr5:109733659
|
T | C | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.707+4146T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733659 | ||||||
| chr5:109733673
|
A | T | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.707+4160A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733673 | ||||||
| chr5:109733675
|
C | T | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.707+4162C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733675 | ||||||
| chr5:109733699
|
C | A | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.707+4186C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733699 | ||||||
| chr5:109733751
|
T | G | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.707+4238T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733751 | ||||||
| chr5:109733764
|
C | T | 1 | a0001c0009t0001g0208 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.707+4251C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733764 | ||||||
| chr5:109733871
|
C | T | 31 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(28): Show | 32 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.707+4358C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733871 | ||||||
| chr5:109733937
|
G | A | 1 | a0002c0002t0002g0245 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.707+4424G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733937 | ||||||
| chr5:109733970
|
C | T | 1 | a0001c0006t0002g0278 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.707+4457C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109733970 | ||||||
| chr5:109734118
|
C | A | 3 | a0001c0004t0004g0051a0001c0004t0004g0053a0001c0004t0029g0052 | 3 | HG02258.hp2 HG02896.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.707+4605C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734118 | ||||||
| chr5:109734120
|
T | C | 1 | a0001c0004t0004g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.707+4607T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734120 | ||||||
| chr5:109734148
|
G | A | 86 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0055others(83): Show | 88 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.707+4635G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734148 | ||||||
| chr5:109734198
|
C | T | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.707+4685C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734198 | ||||||
| chr5:109734200
|
G | C | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.707+4687G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734200 | ||||||
| chr5:109734232
|
G | A | 3 | a0001c0004t0004g0051a0001c0004t0004g0053a0001c0004t0029g0052 | 3 | HG02258.hp2 HG02896.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.707+4719G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734232 | ||||||
| chr5:109734303
|
G | GA | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.707+4803dupA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109734303 | |||||
| chr5:109734303
|
GA | G | 97 | a0001c0001t0001g0104a0001c0003t0003g0209a0001c0004t0013g0049others(94): Show | 98 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.707+4803delA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109734303 | |||||
| chr5:109734323
|
G | C | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.707+4810G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734323 | ||||||
| chr5:109734387
|
G | C | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(221): Show | 229 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.707+4874G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734387 | ||||||
| chr5:109734387
|
G | T | 3 | a0001c0005t0008g0010a0001c0005t0008g0016a0001c0005t0008g0017 | 3 | HG00140.hp1 HG00639.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.707+4874G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734387 | ||||||
| chr5:109734441
|
T | C | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.707+4928T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734441 | ||||||
| chr5:109734463
|
A | G | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.707+4950A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734463 | ||||||
| chr5:109734665
|
A | T | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.707+5152A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734665 | ||||||
| chr5:109734667
|
G | A | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.707+5154G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734667 | ||||||
| chr5:109734745
|
A | G | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.707+5232A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734745 | ||||||
| chr5:109734762
|
A | C | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.707+5249A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734762 | ||||||
| chr5:109734777
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(104): Show | 110 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.707+5264G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734777 | ||||||
| chr5:109734904
|
G | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(104): Show | 110 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.707+5391G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734904 | ||||||
| chr5:109734923
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.707+5410C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734923 | ||||||
| chr5:109734943
|
A | T | 1 | a0002c0002t0002g0244 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.707+5430A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109734943 | ||||||
| chr5:109735157
|
G | C | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.707+5644G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109735157 | ||||||
| chr5:109735209
|
G | C | 2 | a0001c0006t0006g0287a0001c0006t0006g0288 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.707+5696G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109735209 | ||||||
| chr5:109735238
|
C | T | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.707+5725C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109735238 | ||||||
| chr5:109735246
|
T | C | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.707+5733T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109735246 | ||||||
| chr5:109735252
|
G | T | 118 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(115): Show | 120 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.707+5739G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109735252 | ||||||
| chr5:109735274
|
G | A | 10 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0005g0281others(7): Show | 10 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.707+5761G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109735274 | ||||||
| chr5:109735327
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.707+5814A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109735327 | ||||||
| chr5:109735447
|
G | T | 1 | a0001c0001t0005g0077 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.707+5934G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109735447 | ||||||
| chr5:109735507
|
G | C | 7 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(4): Show | 7 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.707+5994G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109735507 | ||||||
| chr5:109735549
|
C | T | 1 | a0003c0007t0001g0198 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.707+6036C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109735549 | ||||||
| chr5:109735576
|
T | C | 1 | a0001c0004t0033g0032 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.707+6063T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109735576 | ||||||
| chr5:109735685
|
G | A | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.707+6172G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109735685 | ||||||
| chr5:109735824
|
G | T | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.707+6311G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109735824 | ||||||
| chr5:109735878
|
G | GT | 18 | a0001c0001t0001g0183a0001c0003t0003g0154a0001c0003t0007g0050others(15): Show | 19 | HG00099.hp1 HG01169.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.707+6386dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109735878 | |||||
| chr5:109735878
|
G | GTT | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(146): Show | 153 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.707+6385_707+6386d others(4): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109735878 | |||||
| chr5:109735878
|
G | GTTT | 40 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0078others(37): Show | 40 | HG00639.hp2 HG01109.hp2 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.707+6384_707+6386d others(5): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109735878 | |||||
| chr5:109735975
|
A | G | 1 | a0002c0002t0002g0244 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.707+6462A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109735975 | ||||||
| chr5:109735993
|
C | T | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.707+6480C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109735993 | ||||||
| chr5:109736006
|
C | T | 1 | a0002c0002t0011g0179 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.707+6493C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109736006 | ||||||
| chr5:109736100
|
G | A | 1 | a0001c0003t0003g0185 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.707+6587G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109736100 | ||||||
| chr5:109736130
|
G | T | 1 | a0001c0016t0020g0112 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.707+6617G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109736130 | ||||||
| chr5:109736263
|
A | C | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.707+6750A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109736263 | ||||||
| chr5:109736470
|
T | C | 2 | a0001c0006t0006g0285a0001c0006t0006g0286 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.707+6957T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109736470 | ||||||
| chr5:109736510
|
G | T | 119 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(116): Show | 121 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.707+6997G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109736510 | ||||||
| chr5:109736511
|
G | C | 119 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(116): Show | 121 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.707+6998G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109736511 | ||||||
| chr5:109736529
|
T | G | 1 | a0001c0003t0019g0180 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.707+7016T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109736529 | ||||||
| chr5:109736717
|
T | A | 1 | a0001c0001t0001g0121 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.707+7204T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109736717 | ||||||
| chr5:109736783
|
A | T | 32 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(29): Show | 33 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.707+7270A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109736783 | ||||||
| chr5:109736787
|
A | T | 10 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0005g0281others(7): Show | 10 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.707+7274A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109736787 | ||||||
| chr5:109736947
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.707+7434A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109736947 | ||||||
| chr5:109737092
|
C | CT | 105 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0055others(102): Show | 107 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.707+7598dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109737092 | |||||
| chr5:109737092
|
C | CTT | 39 | a0001c0001t0001g0103a0001c0004t0004g0001a0001c0004t0004g0031others(36): Show | 40 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.707+7597_707+7598d others(4): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109737092 | |||||
| chr5:109737092
|
C | CTTT | 76 | a0001c0004t0004g0046a0001c0009t0001g0208a0001c0009t0002g0227others(73): Show | 77 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.707+7596_707+7598d others(5): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109737092 | |||||
| chr5:109737150
|
C | G | 2 | a0002c0002t0002g0220a0003c0007t0001g0196 | 2 | HG02129.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.707+7637C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109737150 | ||||||
| chr5:109737153
|
G | A | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.707+7640G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109737153 | ||||||
| chr5:109737286
|
T | A | 77 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(74): Show | 78 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.707+7773T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109737286 | ||||||
| chr5:109737445
|
AT | A | 204 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0055others(201): Show | 208 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.707+7946delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109737445 | |||||
| chr5:109737670
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.707+8157A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109737670 | ||||||
| chr5:109737853
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.707+8340G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109737853 | ||||||
| chr5:109738039
|
C | T | 1 | a0007c0014t0002g0193 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.707+8526C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109738039 | ||||||
| chr5:109738141
|
C | T | 1 | a0001c0006t0002g0278 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.707+8628C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109738141 | ||||||
| chr5:109738201
|
C | T | 1 | a0001c0001t0005g0074 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.707+8688C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109738201 | ||||||
| chr5:109738233
|
G | GT | 11 | a0001c0003t0003g0125a0001c0003t0003g0139a0001c0003t0003g0165others(8): Show | 11 | HG00741.hp2 HG01109.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.707+8738dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109738233 | |||||
| chr5:109738233
|
GT | G | 114 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0055others(111): Show | 116 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.707+8738delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109738233 | |||||
| chr5:109738263
|
T | C | 9 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.707+8750T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109738263 | ||||||
| chr5:109738310
|
A | G | 1 | a0002c0002t0002g0245 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.707+8797A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109738310 | ||||||
| chr5:109738320
|
C | T | 15 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.707+8807C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109738320 | ||||||
| chr5:109738408
|
T | C | 119 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(116): Show | 121 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.707+8895T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109738408 | ||||||
| chr5:109738415
|
T | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | NA18961.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.707+8902T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109738415 | ||||||
| chr5:109738473
|
T | G | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.707+8960T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109738473 | ||||||
| chr5:109738700
|
A | G | 1 | a0001c0001t0030g0085 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.707+9187A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109738700 | ||||||
| chr5:109738720
|
C | A | 1 | a0001c0003t0003g0160 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.707+9207C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109738720 | ||||||
| chr5:109738772
|
CT | C | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.707+9262delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109738772 | |||||
| chr5:109738907
|
G | A | 3 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0035g0013 | 3 | HG01109.hp2 HG02257.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.707+9394G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109738907 | ||||||
| chr5:109738928
|
C | T | 1 | a0001c0006t0006g0038 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.707+9415C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109738928 | ||||||
| chr5:109738932
|
C | T | 31 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(28): Show | 32 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.707+9419C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109738932 | ||||||
| chr5:109738943
|
A | G | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.707+9430A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109738943 | ||||||
| chr5:109738951
|
C | T | 1 | a0002c0002t0002g0189 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.707+9438C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109738951 | ||||||
| chr5:109739209
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.707+9696C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109739209 | ||||||
| chr5:109739444
|
A | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(105): Show | 111 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.707+9931A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109739444 | ||||||
| chr5:109739539
|
T | C | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.707+10026T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109739539 | ||||||
| chr5:109739575
|
T | C | 1 | a0002c0002t0002g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.707+10062T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109739575 | ||||||
| chr5:109739630
|
C | T | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.707+10117C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109739630 | ||||||
| chr5:109739760
|
A | ATTC | 7 | a0002c0002t0002g0246a0002c0002t0002g0249a0002c0002t0002g0251others(4): Show | 7 | HG01123.hp1 HG01975.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.707+10247_707+1024 others(7): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109739760 | ||||||
| chr5:109739761
|
C | A | 7 | a0002c0002t0002g0246a0002c0002t0002g0249a0002c0002t0002g0251others(4): Show | 7 | HG01123.hp1 HG01975.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.707+10248C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109739761 | ||||||
| chr5:109739808
|
C | T | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.707+10295C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109739808 | ||||||
| chr5:109739916
|
G | T | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.707+10403G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109739916 | ||||||
| chr5:109740185
|
G | T | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.707+10672G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109740185 | ||||||
| chr5:109740266
|
A | G | 1 | a0002c0002t0002g0289 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.707+10753A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109740266 | ||||||
| chr5:109740411
|
C | T | 3 | a0001c0005t0010g0014a0001c0005t0010g0015a0001c0005t0010g0018 | 3 | NA18959.hp1 NA19009.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.707+10898C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109740411 | ||||||
| chr5:109740526
|
C | CTTG | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.707+11014_707+1101 others(7): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109740526 | |||||
| chr5:109740562
|
T | A | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.707+11049T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109740562 | ||||||
| chr5:109740588
|
G | A | 9 | a0001c0001t0001g0039a0001c0001t0001g0083a0001c0001t0001g0106others(6): Show | 9 | HG00741.hp1 HG01074.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.707+11075G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109740588 | ||||||
| chr5:109740635
|
C | T | 219 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0055others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.707+11122C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109740635 | ||||||
| chr5:109740715
|
G | A | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.707+11202G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109740715 | ||||||
| chr5:109740727
|
ATCT | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0055others(100): Show | 105 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.707+11219_707+1122 others(7): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109740727 | |||||
| chr5:109740749
|
T | G | 1 | a0001c0003t0003g0129 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.707+11236T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109740749 | ||||||
| chr5:109740787
|
T | C | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.707+11274T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109740787 | ||||||
| chr5:109740815
|
C | T | 6 | a0002c0002t0002g0189a0002c0002t0002g0236a0002c0002t0002g0239others(3): Show | 6 | HG00099.hp2 HG01934.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.707+11302C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109740815 | ||||||
| chr5:109740858
|
G | A | 1 | a0001c0005t0010g0019 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.707+11345G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109740858 | ||||||
| chr5:109740946
|
A | G | 1 | a0002c0002t0002g0252 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.707+11433A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109740946 | ||||||
| chr5:109741019
|
C | T | 32 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(29): Show | 33 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.707+11506C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109741019 | ||||||
| chr5:109741094
|
T | C | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.707+11581T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109741094 | ||||||
| chr5:109741157
|
A | G | 8 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.707+11644A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109741157 | ||||||
| chr5:109741437
|
C | G | 9 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.707+11924C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109741437 | ||||||
| chr5:109741622
|
C | T | 1 | a0001c0003t0003g0150 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.707+12109C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109741622 | ||||||
| chr5:109741816
|
T | C | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.707+12303T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109741816 | ||||||
| chr5:109741853
|
T | C | 28 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(25): Show | 29 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.707+12340T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109741853 | ||||||
| chr5:109741990
|
G | C | 31 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(28): Show | 32 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.707+12477G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109741990 | ||||||
| chr5:109742062
|
A | G | 1 | a0001c0004t0004g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.707+12549A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109742062 | ||||||
| chr5:109742145
|
T | C | 2 | a0001c0003t0003g0137a0001c0003t0003g0192 | 2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.707+12632T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109742145 | ||||||
| chr5:109742169
|
G | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0104 | 2 | NA19080.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.707+12656G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109742169 | ||||||
| chr5:109742305
|
G | A | 1 | a0002c0002t0027g0234 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.707+12792G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109742305 | ||||||
| chr5:109742339
|
G | A | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.707+12826G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109742339 | ||||||
| chr5:109742385
|
G | C | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.707+12872G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109742385 | ||||||
| chr5:109742420
|
T | TATA | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.707+12907_707+1290 others(7): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109742420 | ||||||
| chr5:109742502
|
C | G | 1 | a0001c0003t0007g0136 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.708-12827C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109742502 | ||||||
| chr5:109742886
|
A | G | 1 | a0001c0006t0006g0172 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.708-12443A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109742886 | ||||||
| chr5:109742904
|
C | G | 1 | a0001c0001t0001g0082 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.708-12425C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109742904 | ||||||
| chr5:109742997
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.708-12332C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109742997 | ||||||
| chr5:109743011
|
T | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(224): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.708-12318T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109743011 | ||||||
| chr5:109743212
|
A | G | 15 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.708-12117A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109743212 | ||||||
| chr5:109743215
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.708-12114T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109743215 | ||||||
| chr5:109743230
|
G | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.708-12099G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109743230 | ||||||
| chr5:109743379
|
G | A | 1 | a0001c0006t0006g0172 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.708-11950G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109743379 | ||||||
| chr5:109743409
|
C | G | 12 | a0001c0009t0002g0227a0002c0002t0002g0178a0002c0002t0002g0219others(9): Show | 12 | HG00597.hp2 HG02135.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.708-11920C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109743409 | ||||||
| chr5:109743523
|
GC | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.708-11804delC | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109743523 | |||||
| chr5:109743525
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.708-11804C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109743525 | ||||||
| chr5:109743666
|
C | T | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.708-11663C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109743666 | ||||||
| chr5:109743696
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.708-11633G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109743696 | ||||||
| chr5:109743756
|
C | A | 5 | a0001c0006t0006g0172a0001c0006t0006g0285a0001c0006t0006g0286others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.708-11573C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109743756 | ||||||
| chr5:109743892
|
G | C | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.708-11437G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109743892 | ||||||
| chr5:109743902
|
G | A | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.708-11427G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109743902 | ||||||
| chr5:109743957
|
C | T | 2 | a0002c0002t0017g0275a0002c0002t0017g0276 | 2 | NA18959.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.708-11372C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109743957 | ||||||
| chr5:109744376
|
G | C | 1 | a0004c0008t0014g0023 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.708-10953G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109744376 | ||||||
| chr5:109744762
|
A | G | 1 | a0002c0002t0002g0237 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.708-10567A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109744762 | ||||||
| chr5:109745128
|
C | T | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.708-10201C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109745128 | ||||||
| chr5:109745223
|
G | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.708-10106G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109745223 | ||||||
| chr5:109745466
|
G | A | 4 | a0001c0006t0006g0285a0001c0006t0006g0286a0001c0006t0006g0287others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.708-9863G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109745466 | ||||||
| chr5:109746506
|
G | A | 4 | a0001c0003t0003g0156a0001c0003t0003g0157a0001c0003t0003g0159others(1): Show | 4 | HG01192.hp2 HG01433.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.708-8823G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109746506 | ||||||
| chr5:109746513
|
T | C | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.708-8816T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109746513 | ||||||
| chr5:109746530
|
A | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073 | 3 | NA18952.hp1 NA18961.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.708-8799A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109746530 | ||||||
| chr5:109746572
|
G | GT | 21 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0005g0111others(18): Show | 22 | HG01123.hp2 HG01243.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.708-8739dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109746572 | |||||
| chr5:109746572
|
G | GTT | 12 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.708-8740_708-8739d others(4): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109746572 | |||||
| chr5:109746572
|
GT | G | 9 | a0001c0001t0001g0072a0001c0001t0030g0085a0001c0003t0003g0130others(6): Show | 10 | HG01192.hp1 HG01257.hp1 HG03017.hp1 others(7): Show |
intron_variant | MODIFIER | c.708-8739delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109746572 | |||||
| chr5:109746654
|
T | G | 1 | a0001c0003t0007g0136 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.708-8675T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109746654 | ||||||
| chr5:109746699
|
T | C | 3 | a0001c0003t0003g0160a0001c0003t0003g0161a0001c0003t0003g0167 | 3 | HG02056.hp1 NA18966.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.708-8630T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109746699 | ||||||
| chr5:109746717
|
G | A | 1 | a0002c0002t0002g0206 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.708-8612G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109746717 | ||||||
| chr5:109746724
|
G | A | 119 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(116): Show | 121 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.708-8605G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109746724 | ||||||
| chr5:109746752
|
C | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(102): Show | 109 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.708-8577C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109746752 | ||||||
| chr5:109746796
|
G | C | 1 | a0001c0005t0010g0014 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.708-8533G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109746796 | ||||||
| chr5:109746835
|
G | C | 1 | a0001c0003t0003g0129 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.708-8494G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109746835 | ||||||
| chr5:109746893
|
T | C | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.708-8436T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109746893 | ||||||
| chr5:109746895
|
C | G | 3 | a0002c0002t0002g0202a0002c0002t0002g0203a0002c0002t0002g0204 | 3 | NA18957.hp2 NA18969.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.708-8434C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109746895 | ||||||
| chr5:109746973
|
C | T | 7 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(4): Show | 7 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.708-8356C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109746973 | ||||||
| chr5:109747032
|
A | G | 15 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.708-8297A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109747032 | ||||||
| chr5:109747155
|
C | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.708-8174C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109747155 | ||||||
| chr5:109747185
|
A | G | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.708-8144A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109747185 | ||||||
| chr5:109747216
|
C | T | 1 | a0002c0002t0034g0218 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.708-8113C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109747216 | ||||||
| chr5:109747291
|
TAAGC | T | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.708-8036_708-8033d others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109747291 | |||||
| chr5:109747421
|
G | A | 119 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(116): Show | 121 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.708-7908G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109747421 | ||||||
| chr5:109747471
|
A | G | 1 | a0002c0002t0011g0179 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.708-7858A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109747471 | ||||||
| chr5:109747541
|
A | G | 1 | a0003c0007t0001g0196 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.708-7788A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109747541 | ||||||
| chr5:109747980
|
G | A | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.708-7349G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109747980 | ||||||
| chr5:109748057
|
G | A | 115 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(112): Show | 117 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.708-7272G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109748057 | ||||||
| chr5:109748066
|
G | A | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.708-7263G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109748066 | ||||||
| chr5:109748098
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.708-7231T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109748098 | ||||||
| chr5:109748401
|
CT | C | 35 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0003t0003g0156others(32): Show | 36 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.708-6914delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109748401 | |||||
| chr5:109748724
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.708-6605A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109748724 | ||||||
| chr5:109749067
|
T | C | 1 | a0002c0002t0002g0246 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.708-6262T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109749067 | ||||||
| chr5:109749106
|
T | G | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.708-6223T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109749106 | ||||||
| chr5:109749501
|
A | G | 2 | a0002c0002t0002g0202a0002c0002t0002g0203 | 2 | NA18969.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.708-5828A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109749501 | ||||||
| chr5:109749790
|
C | T | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.708-5539C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109749790 | ||||||
| chr5:109749984
|
G | A | 77 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(74): Show | 78 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.708-5345G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109749984 | ||||||
| chr5:109749991
|
G | C | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.708-5338G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109749991 | ||||||
| chr5:109750047
|
T | A | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.708-5282T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109750047 | ||||||
| chr5:109750158
|
T | G | 1 | a0002c0002t0009g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.708-5171T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109750158 | ||||||
| chr5:109750314
|
A | G | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.708-5015A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109750314 | ||||||
| chr5:109750455
|
T | A | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.708-4874T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109750455 | ||||||
| chr5:109750491
|
A | G | 1 | a0001c0003t0003g0149 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.708-4838A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109750491 | ||||||
| chr5:109750623
|
T | C | 2 | a0001c0004t0004g0047a0001c0004t0004g0048 | 2 | HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.708-4706T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109750623 | ||||||
| chr5:109751019
|
A | C | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.708-4310A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109751019 | ||||||
| chr5:109751160
|
C | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.708-4169C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109751160 | ||||||
| chr5:109751207
|
T | A | 7 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(4): Show | 7 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.708-4122T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109751207 | ||||||
| chr5:109751336
|
G | T | 34 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(31): Show | 35 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.708-3993G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109751336 | ||||||
| chr5:109751705
|
C | T | 34 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(31): Show | 35 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.708-3624C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109751705 | ||||||
| chr5:109751735
|
T | C | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.708-3594T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109751735 | ||||||
| chr5:109751739
|
C | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.708-3590C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109751739 | ||||||
| chr5:109751791
|
C | T | 1 | a0002c0002t0002g0253 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.708-3538C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109751791 | ||||||
| chr5:109751794
|
T | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.708-3535T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109751794 | ||||||
| chr5:109751972
|
T | C | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.708-3357T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109751972 | ||||||
| chr5:109752386
|
C | T | 1 | a0001c0005t0035g0013 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.708-2943C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109752386 | ||||||
| chr5:109752655
|
G | C | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.708-2674G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109752655 | ||||||
| chr5:109752682
|
A | G | 1 | a0002c0002t0002g0229 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.708-2647A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109752682 | ||||||
| chr5:109752694
|
A | G | 1 | a0001c0013t0003g0155 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.708-2635A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109752694 | ||||||
| chr5:109752697
|
G | T | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.708-2632G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109752697 | ||||||
| chr5:109752738
|
A | T | 1 | a0001c0003t0003g0138 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.708-2591A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109752738 | ||||||
| chr5:109752852
|
G | A | 235 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0055others(232): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.708-2477G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109752852 | ||||||
| chr5:109752859
|
A | G | 28 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(25): Show | 29 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.708-2470A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109752859 | ||||||
| chr5:109752920
|
G | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0055others(115): Show | 121 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.708-2409G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109752920 | ||||||
| chr5:109752989
|
A | G | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.708-2340A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109752989 | ||||||
| chr5:109753076
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.708-2253A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109753076 | ||||||
| chr5:109753143
|
A | AC | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0290 | 3 | HG02896.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.708-2186_708-2185i others(3): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109753143 | ||||||
| chr5:109753239
|
G | A | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.708-2090G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109753239 | ||||||
| chr5:109753260
|
T | A | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.708-2069T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109753260 | ||||||
| chr5:109753385
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.708-1944G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109753385 | ||||||
| chr5:109753514
|
A | G | 1 | a0001c0001t0005g0077 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.708-1815A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109753514 | ||||||
| chr5:109753518
|
G | A | 1 | a0001c0004t0013g0214 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.708-1811G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109753518 | ||||||
| chr5:109753782
|
G | T | 1 | a0001c0003t0003g0126 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.708-1547G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109753782 | ||||||
| chr5:109753792
|
T | G | 1 | a0002c0002t0002g0206 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.708-1537T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109753792 | ||||||
| chr5:109753849
|
G | A | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.708-1480G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109753849 | ||||||
| chr5:109753973
|
A | G | 1 | a0002c0002t0002g0205 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.708-1356A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109753973 | ||||||
| chr5:109754011
|
C | CA | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.708-1316dupA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109754011 | |||||
| chr5:109754052
|
G | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0055others(100): Show | 105 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.708-1277G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109754052 | ||||||
| chr5:109754274
|
A | AT | 5 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282others(2): Show | 6 | HG01192.hp1 HG02293.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.708-1045dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109754274 | |||||
| chr5:109754477
|
A | G | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.708-852A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109754477 | ||||||
| chr5:109754500
|
G | A | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.708-829G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109754500 | ||||||
| chr5:109754661
|
T | C | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.708-668T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109754661 | ||||||
| chr5:109754728
|
G | A | 5 | a0001c0006t0006g0038a0001c0006t0006g0285a0001c0006t0006g0286others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.708-601G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109754728 | ||||||
| chr5:109754740
|
G | A | 10 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0005g0281others(7): Show | 10 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.708-589G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109754740 | ||||||
| chr5:109754831
|
G | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0055others(100): Show | 105 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.708-498G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109754831 | ||||||
| chr5:109754927
|
G | GGAGGCGG others(10): Show |
9 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.708-398_708-382dup others(17): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109754927 | |||||
| chr5:109754932
|
C | T | 101 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0055others(98): Show | 103 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.708-397C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109754932 | ||||||
| chr5:109754933
|
G | A | 1 | a0001c0003t0003g0213 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.708-396G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109754933 | ||||||
| chr5:109754978
|
G | A | 1 | a0002c0002t0002g0240 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.708-351G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109754978 | ||||||
| chr5:109755043
|
A | G | 6 | a0001c0006t0006g0038a0001c0006t0006g0172a0001c0006t0006g0285others(3): Show | 6 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.708-286A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109755043 | ||||||
| chr5:109755125
|
A | G | 1 | a0001c0004t0013g0214 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.708-204A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109755125 | ||||||
| chr5:109755133
|
G | A | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.708-196G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109755133 | ||||||
| chr5:109755150
|
G | A | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.708-179G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109755150 | ||||||
| chr5:109755216
|
G | A | 7 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(4): Show | 7 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.708-113G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | chr5 | 109755216 | ||||||
| chr5:109755230
|
T | TA | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.708-98dupA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 109755230 | |||||
| chr5:109755577
|
T | A | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.835+121T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109755577 | ||||||
| chr5:109755728
|
TTGA | T | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.835+276_835+278del others(3): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109755728 | |||||
| chr5:109755767
|
G | GT | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.835+321dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109755767 | |||||
| chr5:109755832
|
C | T | 219 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0055others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.835+376C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109755832 | ||||||
| chr5:109755916
|
T | A | 83 | a0001c0001t0001g0063a0001c0001t0005g0074a0001c0009t0001g0208others(80): Show | 84 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.835+460T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109755916 | ||||||
| chr5:109755917
|
T | C | 6 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 6 | HG02647.hp1 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.835+461T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109755917 | ||||||
| chr5:109755947
|
A | G | 1 | a0010c0020t0003g0174 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.835+491A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109755947 | ||||||
| chr5:109755956
|
G | A | 1 | a0001c0001t0005g0111 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.835+500G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109755956 | ||||||
| chr5:109755987
|
A | G | 1 | a0001c0005t0035g0013 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.835+531A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109755987 | ||||||
| chr5:109756113
|
A | G | 83 | a0001c0001t0001g0063a0001c0001t0005g0074a0001c0009t0001g0208others(80): Show | 84 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.835+657A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109756113 | ||||||
| chr5:109756144
|
C | G | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.835+688C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109756144 | ||||||
| chr5:109756387
|
TGTA | T | 8 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.835+934_835+936del others(3): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109756387 | |||||
| chr5:109756441
|
T | C | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.835+985T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109756441 | ||||||
| chr5:109756489
|
T | C | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.835+1033T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109756489 | ||||||
| chr5:109756569
|
C | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.835+1113C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109756569 | ||||||
| chr5:109756689
|
G | A | 6 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 6 | HG02647.hp1 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.835+1233G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109756689 | ||||||
| chr5:109756746
|
C | T | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.835+1290C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109756746 | ||||||
| chr5:109756893
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.835+1437A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109756893 | ||||||
| chr5:109757038
|
G | A | 32 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(29): Show | 33 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.835+1582G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109757038 | ||||||
| chr5:109757101
|
T | C | 32 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(29): Show | 33 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.835+1645T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109757101 | ||||||
| chr5:109757138
|
T | C | 32 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(29): Show | 33 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.835+1682T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109757138 | ||||||
| chr5:109757160
|
T | C | 32 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(29): Show | 33 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.835+1704T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109757160 | ||||||
| chr5:109757224
|
C | T | 2 | a0001c0005t0010g0015a0001c0005t0010g0018 | 2 | NA19009.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.835+1768C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109757224 | ||||||
| chr5:109757389
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.835+1933C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109757389 | ||||||
| chr5:109758031
|
A | G | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.835+2575A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109758031 | ||||||
| chr5:109758116
|
C | T | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.835+2660C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109758116 | ||||||
| chr5:109758187
|
T | A | 1 | a0002c0002t0009g0200 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.835+2731T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109758187 | ||||||
| chr5:109758197
|
C | T | 4 | a0001c0006t0006g0285a0001c0006t0006g0286a0001c0006t0006g0287others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.835+2741C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109758197 | ||||||
| chr5:109758219
|
A | G | 1 | a0001c0005t0035g0013 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.835+2763A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109758219 | ||||||
| chr5:109758263
|
T | G | 1 | a0002c0002t0002g0248 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.835+2807T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109758263 | ||||||
| chr5:109758327
|
G | A | 1 | a0001c0003t0003g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.835+2871G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109758327 | ||||||
| chr5:109758461
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.835+3005C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109758461 | ||||||
| chr5:109758470
|
G | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.835+3014G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109758470 | ||||||
| chr5:109758486
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.835+3030G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109758486 | ||||||
| chr5:109758503
|
C | T | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.835+3047C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109758503 | ||||||
| chr5:109758673
|
T | C | 1 | a0001c0003t0003g0127 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.835+3217T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109758673 | ||||||
| chr5:109759226
|
G | A | 235 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0055others(232): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.835+3770G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109759226 | ||||||
| chr5:109759241
|
C | A | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.835+3785C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109759241 | ||||||
| chr5:109759548
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.835+4092G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109759548 | ||||||
| chr5:109759630
|
G | A | 22 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0096others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.835+4174G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109759630 | ||||||
| chr5:109759726
|
T | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(96): Show | 103 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.835+4270T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109759726 | ||||||
| chr5:109759753
|
C | T | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.835+4297C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109759753 | ||||||
| chr5:109759844
|
T | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(97): Show | 104 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.835+4388T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109759844 | ||||||
| chr5:109759857
|
T | G | 1 | a0002c0002t0002g0247 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.835+4401T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109759857 | ||||||
| chr5:109759863
|
T | A | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.835+4407T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109759863 | ||||||
| chr5:109759947
|
CTA | C | 12 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0109others(9): Show | 12 | HG00099.hp1 HG01109.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.835+4508_835+4509d others(4): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759947 | |||||
| chr5:109759947
|
CTATA | C | 4 | a0001c0003t0003g0128a0001c0003t0003g0143a0001c0003t0003g0145others(1): Show | 4 | HG01069.hp1 HG03490.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.835+4506_835+4509d others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759947 | |||||
| chr5:109759947
|
CTATATA | C | 13 | a0001c0003t0003g0148a0001c0006t0002g0279a0002c0002t0002g0205others(10): Show | 13 | HG00733.hp2 HG01891.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.835+4504_835+4509d others(8): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759947 | |||||
| chr5:109759947
|
CTATATAT others(1): Show |
C | 3 | a0001c0003t0003g0164a0001c0003t0003g0165a0001c0003t0019g0180 | 3 | HG00741.hp2 HG01255.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.835+4502_835+4509d others(10): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759947 | |||||
| chr5:109759947
|
CTATATAT others(3): Show |
C | 56 | a0001c0003t0003g0207a0001c0009t0001g0208a0001c0009t0002g0227others(53): Show | 57 | HG00099.hp2 HG00609.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.835+4500_835+4509d others(12): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759947 | |||||
| chr5:109759947
|
CTATATAT others(7): Show |
C | 2 | a0002c0002t0002g0258a0002c0002t0002g0259 | 2 | HG01433.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.835+4496_835+4509d others(16): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759947 | |||||
| chr5:109759952
|
TATATATA others(7): Show |
T | 7 | a0002c0002t0002g0204a0002c0002t0002g0229a0002c0002t0002g0255others(4): Show | 7 | HG00438.hp2 HG00597.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.835+4500_835+4513d others(16): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759952 | |||||
| chr5:109759952
|
TATATATA others(11): Show |
T | 2 | a0002c0002t0002g0222a0002c0002t0026g0231 | 2 | NA18952.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.835+4500_835+4517d others(20): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759952 | |||||
| chr5:109759952
|
TATATATA others(15): Show |
T | 1 | a0002c0002t0002g0271 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.835+4500_835+4521d others(24): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759952 | |||||
| chr5:109759954
|
TATATATA others(5): Show |
T | 4 | a0001c0003t0003g0129a0001c0003t0003g0201a0001c0003t0003g0209others(1): Show | 4 | HG01167.hp1 HG01257.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+4502_835+4513d others(14): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759954 | |||||
| chr5:109759956
|
TATATATA others(3): Show |
T | 7 | a0001c0001t0001g0003a0001c0001t0001g0056a0001c0001t0001g0091others(4): Show | 8 | HG01255.hp2 HG02451.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.835+4504_835+4513d others(12): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759956 | |||||
| chr5:109759956
|
TATATATA others(7): Show |
T | 98 | a0001c0001t0001g0002a0001c0001t0001g0055a0001c0001t0001g0057others(95): Show | 101 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.835+4504_835+4517d others(16): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759956 | |||||
| chr5:109759956
|
TATATATA others(11): Show |
T | 27 | a0001c0001t0001g0039a0001c0001t0001g0087a0001c0001t0001g0088others(24): Show | 28 | HG01192.hp1 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.835+4504_835+4521d others(20): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759956 | |||||
| chr5:109759956
|
TATATATA others(15): Show |
T | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.835+4504_835+4525d others(24): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759956 | |||||
| chr5:109759958
|
T | G | 3 | a0002c0002t0002g0178a0002c0002t0002g0221a0002c0002t0002g0284 | 3 | HG02257.hp1 HG02300.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.835+4502T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109759958 | ||||||
| chr5:109759958
|
TATATATA others(5): Show |
T | 2 | a0001c0003t0003g0130a0001c0003t0003g0132 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.835+4506_835+4517d others(14): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759958 | |||||
| chr5:109759960
|
TATATAG | T | 5 | a0001c0005t0008g0010a0001c0005t0008g0012a0001c0005t0008g0016others(2): Show | 5 | HG00140.hp1 HG00639.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.835+4508_835+4513d others(8): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759960 | |||||
| chr5:109759960
|
TATATAGA others(3): Show |
T | 5 | a0001c0004t0013g0214a0001c0005t0008g0009a0001c0005t0010g0014others(2): Show | 5 | HG02055.hp1 HG03139.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.835+4508_835+4517d others(12): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759960 | |||||
| chr5:109759962
|
T | G | 19 | a0001c0001t0001g0109a0001c0003t0003g0128a0001c0003t0003g0145others(16): Show | 19 | HG00140.hp2 HG00733.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.835+4506T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109759962 | ||||||
| chr5:109759962
|
T | TATAG | 6 | a0001c0003t0003g0134a0001c0003t0003g0135a0001c0003t0003g0159others(3): Show | 6 | HG00642.hp2 HG01074.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.835+4546_835+4549d others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759962 | |||||
| chr5:109759962
|
TATAGATA others(5): Show |
T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.835+4538_835+4549d others(14): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109759962 | |||||
| chr5:109759974
|
G | T | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.835+4518G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109759974 | ||||||
| chr5:109760295
|
T | A | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.835+4839T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109760295 | ||||||
| chr5:109760306
|
A | G | 1 | a0001c0001t0005g0058 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.835+4850A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109760306 | ||||||
| chr5:109760622
|
A | G | 1 | a0002c0002t0002g0245 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.835+5166A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109760622 | ||||||
| chr5:109760634
|
G | A | 22 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0096others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.835+5178G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109760634 | ||||||
| chr5:109760665
|
G | A | 1 | a0001c0005t0008g0009 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.835+5209G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109760665 | ||||||
| chr5:109760692
|
C | G | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.835+5236C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109760692 | ||||||
| chr5:109760773
|
T | C | 1 | a0001c0004t0015g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.835+5317T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109760773 | ||||||
| chr5:109760822
|
T | A | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.835+5366T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109760822 | ||||||
| chr5:109760841
|
T | C | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.835+5385T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109760841 | ||||||
| chr5:109760920
|
A | C | 1 | a0002c0002t0002g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.835+5464A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109760920 | ||||||
| chr5:109761009
|
C | T | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.835+5553C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109761009 | ||||||
| chr5:109761167
|
A | T | 5 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0098others(2): Show | 5 | HG01243.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.835+5711A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109761167 | ||||||
| chr5:109761211
|
T | C | 7 | a0001c0004t0036g0024a0001c0006t0002g0278a0001c0006t0002g0279others(4): Show | 7 | HG01891.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.835+5755T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109761211 | ||||||
| chr5:109761339
|
G | A | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.835+5883G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109761339 | ||||||
| chr5:109761343
|
CATATT | C | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.835+5892_835+5896d others(7): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109761343 | |||||
| chr5:109761378
|
A | G | 4 | a0001c0004t0036g0024a0004c0008t0014g0021a0004c0008t0014g0022others(1): Show | 4 | HG02717.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+5922A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109761378 | ||||||
| chr5:109761394
|
T | C | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.835+5938T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109761394 | ||||||
| chr5:109761431
|
C | A | 1 | a0001c0001t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.835+5975C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109761431 | ||||||
| chr5:109761515
|
C | T | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.836-6020C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109761515 | ||||||
| chr5:109761572
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(136): Show | 144 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(141): Show |
intron_variant | MODIFIER | c.836-5963A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109761572 | ||||||
| chr5:109761587
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.836-5948T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109761587 | ||||||
| chr5:109761638
|
T | A | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.836-5897T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109761638 | ||||||
| chr5:109761691
|
A | G | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.836-5844A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109761691 | ||||||
| chr5:109761833
|
T | G | 1 | a0001c0004t0004g0043 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.836-5702T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109761833 | ||||||
| chr5:109761985
|
G | A | 120 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(117): Show | 122 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.836-5550G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109761985 | ||||||
| chr5:109762065
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.836-5470T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109762065 | ||||||
| chr5:109762094
|
C | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.836-5441C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109762094 | ||||||
| chr5:109762320
|
T | C | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.836-5215T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109762320 | ||||||
| chr5:109762452
|
T | C | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.836-5083T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109762452 | ||||||
| chr5:109762455
|
T | C | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.836-5080T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109762455 | ||||||
| chr5:109762597
|
A | G | 1 | a0001c0009t0001g0208 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.836-4938A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109762597 | ||||||
| chr5:109762617
|
G | A | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.836-4918G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109762617 | ||||||
| chr5:109762620
|
T | G | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.836-4915T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109762620 | ||||||
| chr5:109762653
|
T | C | 38 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(35): Show | 39 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.836-4882T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109762653 | ||||||
| chr5:109762783
|
A | C | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.836-4752A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109762783 | ||||||
| chr5:109763029
|
T | G | 4 | a0001c0004t0036g0024a0004c0008t0014g0021a0004c0008t0014g0022others(1): Show | 4 | HG02717.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-4506T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109763029 | ||||||
| chr5:109763254
|
A | G | 1 | a0002c0002t0002g0252 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.836-4281A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109763254 | ||||||
| chr5:109763402
|
G | T | 120 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(117): Show | 122 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.836-4133G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109763402 | ||||||
| chr5:109763460
|
A | T | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.836-4075A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109763460 | ||||||
| chr5:109763510
|
T | A | 1 | a0004c0008t0014g0022 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.836-4025T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109763510 | ||||||
| chr5:109763511
|
A | T | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.836-4024A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109763511 | ||||||
| chr5:109763518
|
A | G | 7 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(4): Show | 7 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.836-4017A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109763518 | ||||||
| chr5:109763521
|
TTAG | T | 39 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(36): Show | 40 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.836-4011_836-4009d others(5): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109763521 | |||||
| chr5:109763571
|
A | G | 1 | a0002c0002t0002g0216 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.836-3964A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109763571 | ||||||
| chr5:109763618
|
A | G | 9 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.836-3917A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109763618 | ||||||
| chr5:109763654
|
T | C | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.836-3881T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109763654 | ||||||
| chr5:109763804
|
C | CT | 10 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0005g0281others(7): Show | 10 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.836-3716dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109763804 | |||||
| chr5:109763814
|
T | A | 1 | a0001c0003t0019g0180 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.836-3721T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109763814 | ||||||
| chr5:109763834
|
C | T | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.836-3701C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109763834 | ||||||
| chr5:109763856
|
C | T | 32 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(29): Show | 33 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.836-3679C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109763856 | ||||||
| chr5:109763909
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.836-3626C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109763909 | ||||||
| chr5:109763957
|
G | T | 2 | a0001c0004t0004g0051a0001c0004t0004g0053 | 2 | HG02896.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.836-3578G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109763957 | ||||||
| chr5:109764039
|
G | A | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.836-3496G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109764039 | ||||||
| chr5:109764054
|
G | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0104 | 2 | NA19080.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.836-3481G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109764054 | ||||||
| chr5:109764096
|
C | T | 4 | a0001c0001t0005g0099a0001c0004t0013g0049a0001c0004t0013g0214others(1): Show | 4 | HG01192.hp1 HG03017.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.836-3439C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109764096 | ||||||
| chr5:109764170
|
G | T | 1 | a0002c0002t0026g0231 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.836-3365G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109764170 | ||||||
| chr5:109764190
|
A | G | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.836-3345A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109764190 | ||||||
| chr5:109764197
|
A | G | 1 | a0001c0004t0015g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.836-3338A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109764197 | ||||||
| chr5:109764514
|
A | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.836-3021A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109764514 | ||||||
| chr5:109764646
|
T | C | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.836-2889T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109764646 | ||||||
| chr5:109764677
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.836-2858G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109764677 | ||||||
| chr5:109764753
|
T | C | 1 | a0001c0001t0005g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.836-2782T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109764753 | ||||||
| chr5:109764766
|
A | G | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.836-2769A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109764766 | ||||||
| chr5:109764814
|
T | C | 120 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(117): Show | 122 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.836-2721T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109764814 | ||||||
| chr5:109764843
|
T | A | 1 | a0002c0002t0002g0219 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.836-2692T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109764843 | ||||||
| chr5:109764867
|
T | C | 1 | a0002c0002t0023g0223 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.836-2668T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109764867 | ||||||
| chr5:109764918
|
A | G | 2 | a0001c0004t0004g0211a0001c0004t0015g0210 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.836-2617A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109764918 | ||||||
| chr5:109765042
|
G | A | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.836-2493G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109765042 | ||||||
| chr5:109765049
|
T | G | 120 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(117): Show | 122 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.836-2486T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109765049 | ||||||
| chr5:109765164
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0076 | 2 | HG00438.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.836-2371T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109765164 | ||||||
| chr5:109765165
|
C | T | 39 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(36): Show | 40 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.836-2370C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109765165 | ||||||
| chr5:109765197
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.836-2338C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109765197 | ||||||
| chr5:109765273
|
T | A | 1 | a0002c0002t0025g0263 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.836-2262T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109765273 | ||||||
| chr5:109765425
|
G | A | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.836-2110G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109765425 | ||||||
| chr5:109765505
|
C | G | 5 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(2): Show | 5 | HG01257.hp1 HG02055.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.836-2030C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109765505 | ||||||
| chr5:109765613
|
C | T | 1 | a0001c0006t0006g0172 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.836-1922C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109765613 | ||||||
| chr5:109765755
|
C | A | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(204): Show | 212 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.836-1780C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109765755 | ||||||
| chr5:109765790
|
G | C | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.836-1745G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109765790 | ||||||
| chr5:109765886
|
C | T | 30 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(27): Show | 31 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.836-1649C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109765886 | ||||||
| chr5:109765890
|
A | G | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.836-1645A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109765890 | ||||||
| chr5:109765960
|
T | G | 4 | a0001c0004t0004g0001a0001c0004t0004g0044a0001c0004t0004g0045others(1): Show | 5 | HG01243.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.836-1575T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109765960 | ||||||
| chr5:109766062
|
T | G | 1 | a0001c0001t0005g0058 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.836-1473T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109766062 | ||||||
| chr5:109766128
|
T | G | 1 | a0002c0002t0009g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.836-1407T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109766128 | ||||||
| chr5:109766130
|
C | T | 120 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(117): Show | 122 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.836-1405C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109766130 | ||||||
| chr5:109766170
|
T | G | 77 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(74): Show | 78 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.836-1365T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109766170 | ||||||
| chr5:109766322
|
A | G | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.836-1213A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109766322 | ||||||
| chr5:109766647
|
G | A | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.836-888G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109766647 | ||||||
| chr5:109766693
|
GA | G | 6 | a0001c0004t0036g0024a0001c0006t0002g0278a0001c0006t0002g0279others(3): Show | 6 | HG01891.hp2 HG02451.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.836-834delA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 109766693 | |||||
| chr5:109766700
|
A | C | 1 | a0002c0002t0002g0254 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.836-835A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109766700 | ||||||
| chr5:109766709
|
A | G | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.836-826A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109766709 | ||||||
| chr5:109766987
|
A | G | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.836-548A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109766987 | ||||||
| chr5:109767042
|
T | G | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.836-493T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109767042 | ||||||
| chr5:109767301
|
G | C | 289 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.836-234G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109767301 | ||||||
| chr5:109767338
|
C | T | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.836-197C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109767338 | ||||||
| chr5:109767349
|
G | A | 1 | a0001c0001t0001g0003 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.836-186G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109767349 | ||||||
| chr5:109767394
|
T | C | 2 | a0002c0002t0002g0246a0002c0002t0002g0249 | 2 | NA19003.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.836-141T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 5/21 | chr5 | 109767394 | ||||||
| chr5:109767865
|
G | C | 100 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0055others(97): Show | 103 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.1009+157G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109767865 | ||||||
| chr5:109768013
|
C | G | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1009+305C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109768013 | ||||||
| chr5:109768057
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1009+349A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109768057 | ||||||
| chr5:109768195
|
C | T | 5 | a0001c0006t0002g0278a0001c0006t0002g0279a0004c0008t0014g0021others(2): Show | 5 | HG01891.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1009+487C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109768195 | ||||||
| chr5:109768235
|
GGA | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0055others(84): Show | 89 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.1009+533_1009+534d others(4): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr5 | 109768235 | |||||
| chr5:109768317
|
A | G | 5 | a0001c0006t0002g0278a0001c0006t0002g0279a0004c0008t0014g0021others(2): Show | 5 | HG01891.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1009+609A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109768317 | ||||||
| chr5:109768546
|
C | G | 1 | a0001c0001t0001g0120 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1009+838C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109768546 | ||||||
| chr5:109768574
|
T | C | 1 | a0001c0004t0004g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1009+866T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109768574 | ||||||
| chr5:109768576
|
T | G | 120 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(117): Show | 122 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.1009+868T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109768576 | ||||||
| chr5:109768935
|
G | A | 4 | a0001c0004t0036g0024a0004c0008t0014g0021a0004c0008t0014g0022others(1): Show | 4 | HG02717.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1009+1227G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109768935 | ||||||
| chr5:109768962
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1009+1254C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109768962 | ||||||
| chr5:109769002
|
G | A | 120 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(117): Show | 122 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.1009+1294G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109769002 | ||||||
| chr5:109769119
|
T | C | 2 | a0001c0003t0003g0131a0001c0003t0003g0173 | 2 | HG02145.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1010-1236T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109769119 | ||||||
| chr5:109769132
|
AACCTTTT others(6): Show |
A | 1 | a0002c0002t0002g0241 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1010-1220_1010-120 others(17): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr5 | 109769132 | |||||
| chr5:109769149
|
A | G | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1010-1206A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109769149 | ||||||
| chr5:109769352
|
C | G | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1010-1003C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109769352 | ||||||
| chr5:109769352
|
C | T | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1010-1003C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109769352 | ||||||
| chr5:109769883
|
A | G | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1010-472A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109769883 | ||||||
| chr5:109769919
|
T | C | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1010-436T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109769919 | ||||||
| chr5:109770205
|
G | A | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1010-150G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 6/21 | chr5 | 109770205 | ||||||
| chr5:109770545
|
T | C | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02257.hp1 HG03239.hp1 |
splice_region_variant&intron_variant | LOW | c.1196+4T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109770545 | ||||||
| chr5:109770548
|
A | G | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | splice_region_variant&intron_variant | LOW | c.1196+7A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109770548 | ||||||
| chr5:109770937
|
A | C | 5 | a0001c0006t0006g0038a0001c0006t0006g0285a0001c0006t0006g0286others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1196+396A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109770937 | ||||||
| chr5:109770995
|
C | T | 1 | a0002c0002t0002g0280 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1196+454C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109770995 | ||||||
| chr5:109771141
|
G | A | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1196+600G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109771141 | ||||||
| chr5:109771161
|
A | C | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1196+620A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109771161 | ||||||
| chr5:109771249
|
G | A | 32 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(29): Show | 33 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1196+708G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109771249 | ||||||
| chr5:109771388
|
A | G | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1196+847A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109771388 | ||||||
| chr5:109771457
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1196+916G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109771457 | ||||||
| chr5:109771747
|
G | A | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1196+1206G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109771747 | ||||||
| chr5:109771847
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1196+1306A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109771847 | ||||||
| chr5:109771932
|
A | G | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1196+1391A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109771932 | ||||||
| chr5:109772051
|
T | TG | 31 | a0001c0001t0001g0002a0001c0001t0001g0055a0001c0001t0001g0079others(28): Show | 33 | HG00639.hp1 HG01255.hp2 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.1196+1515dupG | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr5 | 109772051 | |||||
| chr5:109772116
|
C | T | 1 | a0001c0003t0012g0168 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1196+1575C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109772116 | ||||||
| chr5:109772236
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(104): Show | 111 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.1196+1695G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109772236 | ||||||
| chr5:109772237
|
C | A | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1196+1696C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109772237 | ||||||
| chr5:109772419
|
A | G | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1196+1878A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109772419 | ||||||
| chr5:109772449
|
C | T | 15 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1196+1908C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109772449 | ||||||
| chr5:109772450
|
G | C | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1196+1909G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109772450 | ||||||
| chr5:109772581
|
A | C | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1196+2040A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109772581 | ||||||
| chr5:109772632
|
G | A | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1196+2091G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109772632 | ||||||
| chr5:109772868
|
ATCTTTT | A | 10 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0005g0281others(7): Show | 10 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1197-1919_1197-191 others(10): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109772868 | ||||||
| chr5:109772983
|
T | G | 1 | a0001c0004t0004g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1197-1805T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109772983 | ||||||
| chr5:109772988
|
G | A | 2 | a0001c0003t0003g0164a0001c0003t0003g0165 | 2 | HG00741.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1197-1800G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109772988 | ||||||
| chr5:109773038
|
G | A | 23 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(20): Show | 23 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.1197-1750G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109773038 | ||||||
| chr5:109773281
|
G | A | 88 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0055others(85): Show | 90 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.1197-1507G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109773281 | ||||||
| chr5:109773319
|
C | G | 1 | a0001c0009t0001g0208 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1197-1469C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109773319 | ||||||
| chr5:109773394
|
T | C | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1197-1394T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109773394 | ||||||
| chr5:109773416
|
A | G | 1 | a0008c0019t0002g0250 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1197-1372A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109773416 | ||||||
| chr5:109773806
|
C | T | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1197-982C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109773806 | ||||||
| chr5:109774158
|
A | G | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1197-630A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109774158 | ||||||
| chr5:109774216
|
G | A | 2 | a0001c0004t0004g0211a0001c0004t0015g0210 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1197-572G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109774216 | ||||||
| chr5:109774247
|
T | C | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1197-541T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109774247 | ||||||
| chr5:109774474
|
C | A | 289 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1197-314C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109774474 | ||||||
| chr5:109774537
|
T | C | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1197-251T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109774537 | ||||||
| chr5:109774552
|
T | A | 15 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1197-236T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109774552 | ||||||
| chr5:109774589
|
G | A | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1197-199G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 7/21 | chr5 | 109774589 | ||||||
| chr5:109775131
|
A | G | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(185): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1374+166A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109775131 | ||||||
| chr5:109775220
|
C | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1374+255C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109775220 | ||||||
| chr5:109775354
|
C | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1374+389C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109775354 | ||||||
| chr5:109775479
|
CT | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(224): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1374+525delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109775479 | |||||
| chr5:109775530
|
T | C | 1 | a0002c0002t0002g0265 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1374+565T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109775530 | ||||||
| chr5:109775581
|
C | T | 2 | a0002c0002t0002g0247a0002c0002t0002g0253 | 2 | HG02523.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.1374+616C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109775581 | ||||||
| chr5:109775626
|
C | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1374+661C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109775626 | ||||||
| chr5:109775692
|
T | G | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1374+727T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109775692 | ||||||
| chr5:109775782
|
T | A | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1374+817T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109775782 | ||||||
| chr5:109775830
|
A | G | 3 | a0001c0003t0003g0143a0001c0003t0003g0145a0001c0003t0018g0144 | 3 | HG00140.hp2 HG01069.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1374+865A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109775830 | ||||||
| chr5:109775886
|
A | G | 24 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(21): Show | 24 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1374+921A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109775886 | ||||||
| chr5:109775954
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1374+989C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109775954 | ||||||
| chr5:109775983
|
T | C | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1374+1018T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109775983 | ||||||
| chr5:109775992
|
C | T | 1 | a0001c0004t0013g0049 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1374+1027C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109775992 | ||||||
| chr5:109776069
|
CT | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(212): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1374+1118delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109776069 | |||||
| chr5:109776069
|
CTT | C | 9 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0004t0004g0041others(6): Show | 9 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1374+1117_1374+111 others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109776069 | |||||
| chr5:109776096
|
G | A | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1374+1131G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109776096 | ||||||
| chr5:109776177
|
G | A | 1 | a0002c0002t0002g0255 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1374+1212G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109776177 | ||||||
| chr5:109776323
|
A | T | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1374+1358A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109776323 | ||||||
| chr5:109776435
|
A | T | 1 | a0001c0003t0003g0167 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1374+1470A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109776435 | ||||||
| chr5:109776444
|
A | G | 131 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(128): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.1374+1479A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109776444 | ||||||
| chr5:109776564
|
C | T | 1 | a0001c0003t0003g0158 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1374+1599C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109776564 | ||||||
| chr5:109776765
|
G | A | 7 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(4): Show | 7 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1374+1800G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109776765 | ||||||
| chr5:109776981
|
C | G | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1374+2016C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109776981 | ||||||
| chr5:109777187
|
C | T | 1 | a0001c0003t0003g0027 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1374+2222C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109777187 | ||||||
| chr5:109777383
|
T | C | 2 | a0001c0006t0006g0285a0001c0006t0006g0286 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1374+2418T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109777383 | ||||||
| chr5:109777887
|
C | T | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1374+2922C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109777887 | ||||||
| chr5:109777908
|
A | G | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(185): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1374+2943A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109777908 | ||||||
| chr5:109778036
|
G | A | 1 | a0002c0002t0002g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1374+3071G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109778036 | ||||||
| chr5:109778083
|
C | CA | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(104): Show | 110 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1374+3131dupA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109778083 | |||||
| chr5:109778448
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0005g0099 | 2 | HG01074.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1375-2948C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109778448 | ||||||
| chr5:109778453
|
G | A | 6 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 6 | HG02647.hp1 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1375-2943G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109778453 | ||||||
| chr5:109778601
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1375-2795G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109778601 | ||||||
| chr5:109778619
|
A | G | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1375-2777A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109778619 | ||||||
| chr5:109778661
|
A | G | 2 | a0001c0018t0032g0084a0002c0002t0002g0229 | 2 | HG03516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1375-2735A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109778661 | ||||||
| chr5:109779148
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0104 | 2 | NA19080.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1375-2248A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109779148 | ||||||
| chr5:109779300
|
G | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(104): Show | 111 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.1375-2096G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109779300 | ||||||
| chr5:109779310
|
T | C | 1 | a0001c0003t0003g0126 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1375-2086T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109779310 | ||||||
| chr5:109779549
|
ACACACAC others(9): Show |
A | 1 | a0001c0003t0003g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1375-1835_1375-182 others(20): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109779549 | |||||
| chr5:109779565
|
G | GCA | 3 | a0001c0004t0004g0051a0001c0004t0004g0053a0001c0004t0029g0052 | 3 | HG02258.hp2 HG02896.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1375-1814_1375-181 others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109779565 | |||||
| chr5:109779565
|
G | GCACA | 17 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1375-1816_1375-181 others(8): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109779565 | |||||
| chr5:109779565
|
G | GCACACA | 8 | a0001c0003t0003g0129a0001c0004t0013g0049a0001c0004t0013g0214others(5): Show | 8 | HG01192.hp1 HG01257.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1375-1818_1375-181 others(10): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109779565 | |||||
| chr5:109779565
|
G | GCACACAC others(1): Show |
9 | a0001c0004t0004g0001a0001c0004t0004g0034a0001c0004t0004g0041others(6): Show | 10 | HG01243.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1375-1820_1375-181 others(12): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109779565 | |||||
| chr5:109779565
|
G | GCACACAC others(3): Show |
2 | a0001c0004t0004g0047a0001c0004t0004g0048 | 2 | HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1375-1822_1375-181 others(14): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109779565 | |||||
| chr5:109779574
|
CACACACA others(3): Show |
C | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1375-1812_1375-180 others(14): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109779574 | |||||
| chr5:109779576
|
CACACACA others(1): Show |
C | 5 | a0001c0003t0003g0126a0001c0003t0003g0147a0001c0003t0003g0149others(2): Show | 5 | HG02056.hp2 NA18942.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1375-1812_1375-180 others(12): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109779576 | |||||
| chr5:109779578
|
CACACAA | C | 3 | a0001c0003t0003g0207a0006c0012t0001g0028a0006c0012t0001g0029 | 3 | HG03486.hp2 NA18906.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1375-1812_1375-180 others(10): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109779578 | |||||
| chr5:109779580
|
CACAA | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(92): Show | 99 | HG00609.hp1 HG00639.hp1 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.1375-1812_1375-180 others(8): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109779580 | |||||
| chr5:109779582
|
CAA | C | 5 | a0001c0001t0001g0064a0001c0001t0001g0076a0001c0011t0016g0025others(2): Show | 5 | HG00438.hp1 HG02055.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1375-1812_1375-181 others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109779582 | |||||
| chr5:109779584
|
A | C | 30 | a0001c0003t0003g0129a0001c0004t0004g0001a0001c0004t0004g0030others(27): Show | 31 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1375-1812A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109779584 | ||||||
| chr5:109779923
|
C | T | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1375-1473C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109779923 | ||||||
| chr5:109779961
|
G | T | 1 | a0001c0004t0013g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1375-1435G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109779961 | ||||||
| chr5:109779980
|
T | G | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1375-1416T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109779980 | ||||||
| chr5:109780062
|
T | G | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1375-1334T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109780062 | ||||||
| chr5:109780089
|
G | A | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1375-1307G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109780089 | ||||||
| chr5:109780183
|
G | A | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1375-1213G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109780183 | ||||||
| chr5:109780411
|
G | C | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1375-985G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109780411 | ||||||
| chr5:109780510
|
C | CTG | 23 | a0001c0003t0003g0128a0001c0003t0003g0135a0001c0003t0003g0138others(20): Show | 24 | HG00642.hp2 HG01168.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1375-848_1375-847d others(4): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109780510 | |||||
| chr5:109780510
|
C | CTGTG | 7 | a0001c0004t0004g0041a0001c0004t0004g0043a0001c0004t0004g0051others(4): Show | 7 | HG00140.hp1 HG01081.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1375-850_1375-847d others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109780510 | |||||
| chr5:109780510
|
C | CTGTGTGT others(5): Show |
1 | a0001c0006t0006g0172 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1375-858_1375-847d others(14): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109780510 | |||||
| chr5:109780510
|
CTG | C | 92 | a0001c0001t0001g0039a0001c0001t0001g0070a0001c0001t0001g0083others(89): Show | 93 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1375-848_1375-847d others(4): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109780510 | |||||
| chr5:109780510
|
CTGTG | C | 3 | a0001c0009t0028g0008a0002c0002t0002g0212a0002c0002t0002g0264 | 3 | HG02647.hp2 HG02970.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1375-850_1375-847d others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109780510 | |||||
| chr5:109780510
|
CTGTGTG | C | 7 | a0001c0003t0003g0160a0001c0003t0003g0161a0001c0003t0003g0162others(4): Show | 7 | HG00597.hp1 HG02056.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1375-852_1375-847d others(8): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109780510 | |||||
| chr5:109780546
|
G | A | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(179): Show | 187 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.1375-850G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109780546 | ||||||
| chr5:109780546
|
G | GTA | 13 | a0001c0001t0001g0064a0001c0001t0001g0086a0001c0001t0001g0087others(10): Show | 13 | HG00639.hp1 HG01346.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1375-849_1375-848i others(4): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 109780546 | |||||
| chr5:109780550
|
A | G | 4 | a0001c0004t0004g0051a0001c0004t0004g0053a0001c0004t0029g0052others(1): Show | 4 | HG02258.hp2 HG02896.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1375-846A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109780550 | ||||||
| chr5:109780715
|
A | G | 1 | a0001c0001t0005g0077 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1375-681A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109780715 | ||||||
| chr5:109780744
|
A | T | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1375-652A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109780744 | ||||||
| chr5:109780759
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1375-637C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109780759 | ||||||
| chr5:109780936
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1375-460T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109780936 | ||||||
| chr5:109780955
|
A | G | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1375-441A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109780955 | ||||||
| chr5:109780980
|
T | C | 1 | a0001c0003t0003g0128 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1375-416T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109780980 | ||||||
| chr5:109780998
|
T | C | 4 | a0001c0003t0003g0129a0001c0004t0013g0049a0001c0004t0013g0214others(1): Show | 4 | HG01192.hp1 HG01257.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1375-398T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109780998 | ||||||
| chr5:109781092
|
C | T | 8 | a0003c0007t0001g0005a0003c0007t0001g0194a0003c0007t0001g0195others(5): Show | 9 | HG00609.hp1 HG00673.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1375-304C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 8/21 | chr5 | 109781092 | ||||||
| chr5:109781638
|
T | G | 6 | a0002c0002t0002g0246a0002c0002t0002g0249a0002c0002t0002g0251others(3): Show | 6 | HG01123.hp1 HG01975.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.1577+40T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109781638 | ||||||
| chr5:109781737
|
G | T | 1 | a0001c0001t0001g0117 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1577+139G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109781737 | ||||||
| chr5:109781810
|
G | GA | 4 | a0001c0003t0007g0050a0001c0003t0007g0136a0001c0003t0007g0176others(1): Show | 4 | HG01106.hp2 HG03471.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1577+218dupA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr5 | 109781810 | |||||
| chr5:109781862
|
G | A | 4 | a0001c0004t0036g0024a0004c0008t0014g0021a0004c0008t0014g0022others(1): Show | 4 | HG02717.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1577+264G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109781862 | ||||||
| chr5:109781943
|
G | T | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1577+345G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109781943 | ||||||
| chr5:109782099
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1577+501A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109782099 | ||||||
| chr5:109782237
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1577+639A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109782237 | ||||||
| chr5:109782458
|
G | A | 2 | a0001c0004t0029g0052a0001c0004t0036g0024 | 2 | HG02258.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1577+860G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109782458 | ||||||
| chr5:109782503
|
A | G | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1577+905A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109782503 | ||||||
| chr5:109782545
|
T | C | 2 | a0002c0002t0002g0244a0002c0002t0002g0252 | 2 | HG02027.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.1577+947T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109782545 | ||||||
| chr5:109782581
|
C | T | 10 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0005g0281others(7): Show | 10 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1577+983C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109782581 | ||||||
| chr5:109782593
|
A | G | 1 | a0002c0002t0002g0222 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1577+995A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109782593 | ||||||
| chr5:109782668
|
G | C | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1577+1070G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109782668 | ||||||
| chr5:109782767
|
A | G | 1 | a0001c0004t0029g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1577+1169A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109782767 | ||||||
| chr5:109782790
|
G | T | 4 | a0001c0005t0008g0009a0001c0005t0008g0010a0001c0005t0008g0016others(1): Show | 4 | HG00140.hp1 HG00639.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1577+1192G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109782790 | ||||||
| chr5:109783229
|
A | T | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1578-1515A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109783229 | ||||||
| chr5:109783318
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1578-1426C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109783318 | ||||||
| chr5:109783324
|
A | T | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1578-1420A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109783324 | ||||||
| chr5:109783329
|
C | T | 4 | a0001c0004t0036g0024a0004c0008t0014g0021a0004c0008t0014g0022others(1): Show | 4 | HG02717.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578-1415C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109783329 | ||||||
| chr5:109783739
|
T | TTTAAATA others(296): Show |
9 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(6): Show | 10 | HG02280.hp1 HG02717.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1578-991_1578-990i others(305): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr5 | 109783739 | |||||
| chr5:109783739
|
T | TTTAAATA others(297): Show |
9 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1578-991_1578-990i others(306): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr5 | 109783739 | |||||
| chr5:109783739
|
T | TTTAAATA others(298): Show |
4 | a0001c0004t0004g0034a0001c0004t0004g0036a0001c0004t0004g0037others(1): Show | 4 | HG01106.hp1 HG01175.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578-991_1578-990i others(307): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr5 | 109783739 | |||||
| chr5:109783944
|
C | T | 4 | a0001c0003t0003g0129a0001c0004t0013g0049a0001c0004t0013g0214others(1): Show | 4 | HG01192.hp1 HG01257.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578-800C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109783944 | ||||||
| chr5:109783945
|
G | A | 1 | a0001c0003t0007g0050 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1578-799G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109783945 | ||||||
| chr5:109784210
|
A | G | 4 | a0001c0003t0003g0129a0001c0004t0013g0049a0001c0004t0013g0214others(1): Show | 4 | HG01192.hp1 HG01257.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578-534A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109784210 | ||||||
| chr5:109784244
|
A | G | 1 | a0002c0002t0002g0256 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1578-500A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109784244 | ||||||
| chr5:109784340
|
G | A | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1578-404G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109784340 | ||||||
| chr5:109784424
|
T | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1578-320T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109784424 | ||||||
| chr5:109784640
|
T | C | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1578-104T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109784640 | ||||||
| chr5:109784729
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1578-15C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 9/21 | chr5 | 109784729 | ||||||
| chr5:109785034
|
T | C | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1760+108T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109785034 | ||||||
| chr5:109785119
|
A | G | 1 | a0001c0001t0005g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1760+193A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109785119 | ||||||
| chr5:109785251
|
A | C | 4 | a0001c0005t0008g0009a0001c0005t0008g0010a0001c0005t0008g0016others(1): Show | 4 | HG00140.hp1 HG00639.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1760+325A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109785251 | ||||||
| chr5:109785260
|
A | G | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1760+334A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109785260 | ||||||
| chr5:109785334
|
A | G | 7 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0036others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1760+408A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109785334 | ||||||
| chr5:109785513
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1760+587G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109785513 | ||||||
| chr5:109785539
|
A | C | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1760+613A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109785539 | ||||||
| chr5:109785574
|
A | G | 3 | a0001c0003t0003g0143a0001c0003t0003g0145a0001c0003t0018g0144 | 3 | HG00140.hp2 HG01069.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1760+648A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109785574 | ||||||
| chr5:109785755
|
A | G | 1 | a0001c0003t0007g0136 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1760+829A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109785755 | ||||||
| chr5:109785846
|
C | T | 1 | a0001c0006t0002g0278 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1760+920C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109785846 | ||||||
| chr5:109785990
|
T | C | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1760+1064T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109785990 | ||||||
| chr5:109786027
|
T | C | 84 | a0001c0005t0010g0019a0001c0005t0010g0020a0001c0005t0021g0262others(81): Show | 85 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1760+1101T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109786027 | ||||||
| chr5:109786105
|
A | G | 7 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(4): Show | 7 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1760+1179A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109786105 | ||||||
| chr5:109786198
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1760+1272A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109786198 | ||||||
| chr5:109786292
|
G | C | 4 | a0001c0005t0008g0009a0001c0005t0008g0010a0001c0005t0008g0016others(1): Show | 4 | HG00140.hp1 HG00639.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1760+1366G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109786292 | ||||||
| chr5:109786474
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1760+1548T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109786474 | ||||||
| chr5:109786479
|
G | C | 1 | a0001c0001t0001g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1760+1553G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109786479 | ||||||
| chr5:109786521
|
T | C | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1760+1595T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109786521 | ||||||
| chr5:109786755
|
T | C | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1760+1829T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109786755 | ||||||
| chr5:109786878
|
A | G | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(89): Show | 95 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.1760+1952A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109786878 | ||||||
| chr5:109786941
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | NA18983.hp2 NA19080.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1761-1993C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109786941 | ||||||
| chr5:109786985
|
G | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(89): Show | 95 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.1761-1949G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109786985 | ||||||
| chr5:109786997
|
T | C | 12 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(9): Show | 12 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.1761-1937T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109786997 | ||||||
| chr5:109787031
|
G | T | 1 | a0001c0003t0003g0027 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1761-1903G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109787031 | ||||||
| chr5:109787042
|
G | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(89): Show | 95 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.1761-1892G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109787042 | ||||||
| chr5:109787263
|
G | A | 21 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(18): Show | 21 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1761-1671G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109787263 | ||||||
| chr5:109787329
|
A | G | 1 | a0001c0003t0003g0127 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1761-1605A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109787329 | ||||||
| chr5:109787388
|
G | A | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1761-1546G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109787388 | ||||||
| chr5:109787432
|
A | G | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1761-1502A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109787432 | ||||||
| chr5:109787811
|
G | A | 1 | a0002c0002t0002g0269 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1761-1123G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109787811 | ||||||
| chr5:109787814
|
TTAG | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1761-1117_1761-111 others(7): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 109787814 | |||||
| chr5:109788070
|
C | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(115): Show | 121 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1761-864C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109788070 | ||||||
| chr5:109788177
|
A | T | 83 | a0001c0005t0010g0019a0001c0005t0010g0020a0001c0005t0021g0262others(80): Show | 84 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1761-757A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109788177 | ||||||
| chr5:109788186
|
C | T | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1761-748C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109788186 | ||||||
| chr5:109788219
|
G | GA | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(216): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1761-700dupA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 109788219 | |||||
| chr5:109788261
|
G | C | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1761-673G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109788261 | ||||||
| chr5:109788360
|
AT | A | 83 | a0001c0005t0010g0019a0001c0005t0010g0020a0001c0005t0021g0262others(80): Show | 84 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1761-571delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 109788360 | |||||
| chr5:109788428
|
G | T | 1 | a0002c0002t0002g0259 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1761-506G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109788428 | ||||||
| chr5:109788444
|
A | G | 2 | a0001c0003t0003g0124a0001c0003t0003g0125 | 2 | HG01109.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1761-490A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109788444 | ||||||
| chr5:109788521
|
T | C | 1 | a0001c0004t0015g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1761-413T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109788521 | ||||||
| chr5:109788570
|
A | G | 20 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(17): Show | 20 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.1761-364A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109788570 | ||||||
| chr5:109788709
|
G | T | 3 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0018t0032g0084 | 3 | HG01891.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1761-225G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109788709 | ||||||
| chr5:109788787
|
A | G | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1761-147A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 10/21 | chr5 | 109788787 | ||||||
| chr5:109789065
|
A | G | 1 | a0001c0003t0012g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1875+17A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 11/21 | chr5 | 109789065 | ||||||
| chr5:109789086
|
A | G | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1875+38A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 11/21 | chr5 | 109789086 | ||||||
| chr5:109789092
|
A | G | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1875+44A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 11/21 | chr5 | 109789092 | ||||||
| chr5:109789123
|
G | A | 20 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(17): Show | 20 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.1875+75G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 11/21 | chr5 | 109789123 | ||||||
| chr5:109789371
|
C | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(236): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1876-89C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 11/21 | chr5 | 109789371 | ||||||
| chr5:109789557
|
C | G | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1943+30C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109789557 | ||||||
| chr5:109789715
|
T | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(236): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1943+188T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109789715 | ||||||
| chr5:109789928
|
A | G | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1943+401A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109789928 | ||||||
| chr5:109790201
|
T | C | 20 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(17): Show | 20 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.1943+674T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109790201 | ||||||
| chr5:109790287
|
A | G | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1943+760A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109790287 | ||||||
| chr5:109790528
|
G | A | 2 | a0002c0002t0002g0202a0002c0002t0002g0203 | 2 | NA18969.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1943+1001G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109790528 | ||||||
| chr5:109790697
|
T | C | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1943+1170T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109790697 | ||||||
| chr5:109790815
|
T | C | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1943+1288T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109790815 | ||||||
| chr5:109790844
|
T | C | 4 | a0001c0003t0003g0129a0001c0004t0013g0049a0001c0004t0013g0214others(1): Show | 4 | HG01192.hp1 HG01257.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1943+1317T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109790844 | ||||||
| chr5:109791000
|
G | A | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(199): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1943+1473G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109791000 | ||||||
| chr5:109791049
|
A | C | 84 | a0001c0005t0010g0019a0001c0005t0010g0020a0001c0005t0021g0262others(81): Show | 85 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1943+1522A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109791049 | ||||||
| chr5:109791161
|
C | T | 1 | a0001c0013t0003g0155 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1943+1634C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109791161 | ||||||
| chr5:109791283
|
A | G | 1 | a0001c0006t0006g0038 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1943+1756A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109791283 | ||||||
| chr5:109791321
|
C | A | 41 | a0001c0003t0003g0129a0001c0004t0004g0001a0001c0004t0004g0030others(38): Show | 42 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1943+1794C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109791321 | ||||||
| chr5:109791355
|
A | G | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1943+1828A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109791355 | ||||||
| chr5:109791377
|
A | G | 4 | a0001c0003t0003g0129a0001c0004t0013g0049a0001c0004t0013g0214others(1): Show | 4 | HG01192.hp1 HG01257.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1943+1850A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109791377 | ||||||
| chr5:109791412
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1943+1885G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109791412 | ||||||
| chr5:109791640
|
T | A | 1 | a0001c0003t0003g0027 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1943+2113T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109791640 | ||||||
| chr5:109791820
|
A | G | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1943+2293A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109791820 | ||||||
| chr5:109792021
|
G | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1943+2494G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109792021 | ||||||
| chr5:109792036
|
T | C | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1943+2509T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109792036 | ||||||
| chr5:109792092
|
C | T | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1943+2565C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109792092 | ||||||
| chr5:109792100
|
G | A | 10 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(7): Show | 11 | HG01243.hp1 HG02280.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1943+2573G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109792100 | ||||||
| chr5:109792140
|
C | T | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1943+2613C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109792140 | ||||||
| chr5:109792238
|
T | C | 3 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0018t0032g0084 | 3 | HG01891.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1943+2711T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109792238 | ||||||
| chr5:109792294
|
A | T | 11 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0005g0281others(8): Show | 11 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1943+2767A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109792294 | ||||||
| chr5:109792591
|
A | T | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1943+3064A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109792591 | ||||||
| chr5:109792595
|
A | C | 1 | a0002c0002t0002g0254 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1943+3068A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109792595 | ||||||
| chr5:109792910
|
C | G | 1 | a0001c0003t0007g0176 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1943+3383C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109792910 | ||||||
| chr5:109792912
|
A | G | 1 | a0001c0003t0003g0158 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1943+3385A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109792912 | ||||||
| chr5:109792990
|
A | C | 4 | a0001c0003t0003g0129a0001c0004t0013g0049a0001c0004t0013g0214others(1): Show | 4 | HG01192.hp1 HG01257.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1943+3463A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109792990 | ||||||
| chr5:109793064
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(86): Show | 92 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.1943+3537G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109793064 | ||||||
| chr5:109793134
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1943+3607A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109793134 | ||||||
| chr5:109793491
|
C | T | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1943+3964C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109793491 | ||||||
| chr5:109793492
|
A | G | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(239): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1943+3965A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109793492 | ||||||
| chr5:109793608
|
G | A | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(197): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1943+4081G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109793608 | ||||||
| chr5:109794017
|
G | A | 2 | a0002c0002t0009g0007a0002c0002t0009g0215 | 2 | HG00642.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1943+4490G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109794017 | ||||||
| chr5:109794085
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1943+4558G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109794085 | ||||||
| chr5:109794141
|
A | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(237): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1943+4614A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109794141 | ||||||
| chr5:109794187
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1943+4660C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109794187 | ||||||
| chr5:109794319
|
C | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1943+4792C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109794319 | ||||||
| chr5:109794568
|
T | A | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1943+5041T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109794568 | ||||||
| chr5:109794604
|
T | G | 2 | a0003c0007t0001g0005a0003c0007t0001g0197 | 3 | HG02523.hp1 NA18955.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1943+5077T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109794604 | ||||||
| chr5:109794629
|
T | A | 1 | a0001c0001t0001g0106 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1943+5102T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109794629 | ||||||
| chr5:109795171
|
G | C | 1 | a0001c0004t0004g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1943+5644G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109795171 | ||||||
| chr5:109795227
|
T | C | 1 | a0002c0002t0002g0237 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1943+5700T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109795227 | ||||||
| chr5:109795625
|
G | A | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1943+6098G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109795625 | ||||||
| chr5:109795660
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1943+6133A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109795660 | ||||||
| chr5:109795936
|
A | C | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1943+6409A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109795936 | ||||||
| chr5:109795951
|
A | G | 1 | a0001c0001t0005g0058 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1943+6424A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109795951 | ||||||
| chr5:109796377
|
A | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(87): Show | 93 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.1943+6850A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109796377 | ||||||
| chr5:109796417
|
A | G | 1 | a0001c0003t0003g0185 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1943+6890A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109796417 | ||||||
| chr5:109796587
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1943+7060G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109796587 | ||||||
| chr5:109796593
|
TA | T | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(208): Show | 216 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(213): Show |
intron_variant | MODIFIER | c.1943+7068delA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109796593 | |||||
| chr5:109796622
|
C | T | 6 | a0001c0003t0007g0050a0001c0003t0007g0136a0001c0003t0007g0140others(3): Show | 6 | HG01106.hp2 HG01168.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1943+7095C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109796622 | ||||||
| chr5:109796733
|
A | T | 1 | a0008c0019t0002g0250 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1943+7206A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109796733 | ||||||
| chr5:109796735
|
A | C | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1943+7208A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109796735 | ||||||
| chr5:109796760
|
T | C | 74 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(71): Show | 75 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1943+7233T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109796760 | ||||||
| chr5:109796816
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1943+7289T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109796816 | ||||||
| chr5:109796835
|
C | T | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1943+7308C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109796835 | ||||||
| chr5:109796901
|
A | G | 23 | a0001c0001t0005g0110a0001c0004t0004g0001a0001c0004t0004g0030others(20): Show | 24 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1943+7374A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109796901 | ||||||
| chr5:109796934
|
A | C | 3 | a0002c0002t0002g0202a0002c0002t0002g0203a0002c0002t0002g0204 | 3 | NA18957.hp2 NA18969.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1943+7407A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109796934 | ||||||
| chr5:109796993
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1943+7466G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109796993 | ||||||
| chr5:109797155
|
G | C | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1943+7628G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109797155 | ||||||
| chr5:109797261
|
T | A | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(195): Show | 203 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.1943+7734T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109797261 | ||||||
| chr5:109797308
|
CTG | C | 76 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(73): Show | 77 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1943+7782_1943+778 others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109797308 | ||||||
| chr5:109797312
|
G | C | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1943+7785G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109797312 | ||||||
| chr5:109797447
|
T | C | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1943+7920T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109797447 | ||||||
| chr5:109797767
|
A | G | 15 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1943+8240A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109797767 | ||||||
| chr5:109797827
|
G | C | 1 | a0001c0004t0004g0053 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1943+8300G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109797827 | ||||||
| chr5:109797834
|
C | T | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1943+8307C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109797834 | ||||||
| chr5:109798009
|
T | G | 4 | a0001c0003t0003g0124a0001c0003t0003g0125a0001c0003t0003g0142others(1): Show | 4 | HG01109.hp1 HG01175.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1943+8482T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109798009 | ||||||
| chr5:109798050
|
TGAA | T | 15 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1943+8527_1943+852 others(7): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109798050 | |||||
| chr5:109798221
|
C | T | 2 | a0002c0002t0002g0232a0002c0002t0009g0200 | 2 | NA18962.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1943+8694C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109798221 | ||||||
| chr5:109798327
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0100others(1): Show | 5 | HG01361.hp2 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1943+8800A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109798327 | ||||||
| chr5:109798352
|
C | T | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1943+8825C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109798352 | ||||||
| chr5:109798446
|
C | T | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1943+8919C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109798446 | ||||||
| chr5:109798473
|
TG | T | 2 | a0002c0002t0002g0006a0002c0002t0002g0274 | 3 | NA18947.hp2 NA19000.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1943+8947delG | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109798473 | ||||||
| chr5:109798590
|
G | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(103): Show | 109 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1943+9063G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109798590 | ||||||
| chr5:109798670
|
GTTTGT | G | 14 | a0001c0001t0001g0087a0001c0004t0004g0041a0001c0004t0004g0042others(11): Show | 14 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.1943+9167_1943+917 others(9): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109798670 | |||||
| chr5:109798854
|
T | G | 3 | a0001c0006t0006g0038a0002c0002t0002g0247a0002c0002t0002g0253 | 3 | HG02523.hp2 HG03486.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1943+9327T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109798854 | ||||||
| chr5:109798885
|
G | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(86): Show | 92 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.1943+9358G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109798885 | ||||||
| chr5:109799008
|
A | ATGTGTC | 3 | a0003c0007t0001g0005a0003c0007t0001g0197a0003c0007t0001g0198 | 4 | HG02523.hp1 NA18955.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.1943+9483_1943+948 others(10): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109799008 | |||||
| chr5:109799039
|
A | G | 2 | a0001c0001t0001g0106a0001c0016t0020g0112 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1943+9512A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109799039 | ||||||
| chr5:109799087
|
G | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(88): Show | 94 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1943+9560G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109799087 | ||||||
| chr5:109799131
|
C | T | 26 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(23): Show | 26 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1943+9604C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109799131 | ||||||
| chr5:109799144
|
G | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(88): Show | 94 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1943+9617G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109799144 | ||||||
| chr5:109799154
|
A | G | 1 | a0001c0016t0020g0112 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1943+9627A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109799154 | ||||||
| chr5:109799162
|
C | A | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1943+9635C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109799162 | ||||||
| chr5:109799180
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1943+9653G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109799180 | ||||||
| chr5:109799272
|
T | C | 1 | a0001c0001t0005g0074 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1943+9745T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109799272 | ||||||
| chr5:109799659
|
C | T | 1 | a0002c0002t0002g0219 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1943+10132C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109799659 | ||||||
| chr5:109799702
|
C | T | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1943+10175C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109799702 | ||||||
| chr5:109799754
|
C | CA | 84 | a0001c0003t0003g0129a0001c0004t0013g0049a0001c0004t0013g0214others(81): Show | 85 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1943+10241dupA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109799754 | |||||
| chr5:109799795
|
A | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(88): Show | 94 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1943+10268A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109799795 | ||||||
| chr5:109799945
|
G | A | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1943+10418G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109799945 | ||||||
| chr5:109800088
|
CA | C | 85 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0005g0110others(82): Show | 86 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1943+10579delA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109800088 | |||||
| chr5:109800088
|
CAA | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(107): Show | 114 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.1943+10578_1943+10 others(8): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109800088 | |||||
| chr5:109800137
|
G | A | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1943+10610G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109800137 | ||||||
| chr5:109800143
|
G | GCA | 4 | a0001c0003t0003g0129a0001c0004t0013g0049a0001c0004t0013g0214others(1): Show | 4 | HG01192.hp1 HG01257.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1943+10625_1943+10 others(8): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109800143 | |||||
| chr5:109800324
|
G | A | 76 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(73): Show | 77 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1943+10797G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109800324 | ||||||
| chr5:109800517
|
A | C | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(228): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1943+10990A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109800517 | ||||||
| chr5:109800567
|
G | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(88): Show | 94 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1943+11040G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109800567 | ||||||
| chr5:109800841
|
A | G | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(168): Show | 175 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.1943+11314A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109800841 | ||||||
| chr5:109800912
|
T | G | 1 | a0003c0007t0001g0194 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1943+11385T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109800912 | ||||||
| chr5:109800929
|
C | A | 23 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(20): Show | 23 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.1943+11402C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109800929 | ||||||
| chr5:109800930
|
C | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(88): Show | 94 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1943+11403C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109800930 | ||||||
| chr5:109800958
|
C | T | 7 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(4): Show | 7 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1943+11431C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109800958 | ||||||
| chr5:109801007
|
G | A | 26 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(23): Show | 26 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1943+11480G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109801007 | ||||||
| chr5:109801260
|
G | C | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1943+11733G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109801260 | ||||||
| chr5:109801283
|
G | T | 279 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(276): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1943+11756G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109801283 | ||||||
| chr5:109801536
|
G | A | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1943+12009G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109801536 | ||||||
| chr5:109801619
|
G | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(88): Show | 94 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1943+12092G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109801619 | ||||||
| chr5:109801743
|
A | T | 15 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1943+12216A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109801743 | ||||||
| chr5:109801835
|
T | A | 9 | a0001c0001t0001g0039a0001c0001t0001g0083a0001c0001t0001g0106others(6): Show | 9 | HG00741.hp1 HG01074.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1943+12308T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109801835 | ||||||
| chr5:109801936
|
ATATT | A | 4 | a0001c0003t0003g0129a0001c0004t0013g0049a0001c0004t0013g0214others(1): Show | 4 | HG01192.hp1 HG01257.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1943+12414_1943+12 others(10): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109801936 | |||||
| chr5:109802009
|
T | C | 1 | a0002c0002t0002g0256 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1943+12482T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109802009 | ||||||
| chr5:109802025
|
A | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1943+12498A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109802025 | ||||||
| chr5:109802107
|
C | A | 10 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(7): Show | 11 | HG01243.hp1 HG02280.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1943+12580C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109802107 | ||||||
| chr5:109802219
|
G | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(101): Show | 108 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.1943+12692G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109802219 | ||||||
| chr5:109802342
|
C | T | 28 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(25): Show | 29 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1943+12815C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109802342 | ||||||
| chr5:109802489
|
C | A | 4 | a0001c0003t0003g0129a0001c0004t0013g0049a0001c0004t0013g0214others(1): Show | 4 | HG01192.hp1 HG01257.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1943+12962C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109802489 | ||||||
| chr5:109802701
|
AC | A | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1943+13177delC | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109802701 | |||||
| chr5:109802764
|
G | A | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1943+13237G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109802764 | ||||||
| chr5:109802777
|
T | G | 1 | a0001c0006t0006g0172 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1943+13250T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109802777 | ||||||
| chr5:109802817
|
A | G | 4 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0096others(1): Show | 4 | HG02258.hp1 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1943+13290A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109802817 | ||||||
| chr5:109802847
|
C | T | 11 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0005g0281others(8): Show | 11 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1943+13320C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109802847 | ||||||
| chr5:109802859
|
C | G | 1 | a0001c0001t0001g0003 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1943+13332C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109802859 | ||||||
| chr5:109803096
|
C | A | 4 | a0001c0004t0004g0001a0001c0004t0004g0044a0001c0004t0004g0045others(1): Show | 5 | HG01243.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1943+13569C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109803096 | ||||||
| chr5:109803577
|
T | C | 4 | a0001c0003t0003g0129a0001c0004t0013g0049a0001c0004t0013g0214others(1): Show | 4 | HG01192.hp1 HG01257.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1944-13696T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109803577 | ||||||
| chr5:109803634
|
T | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(200): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1944-13639T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109803634 | ||||||
| chr5:109803727
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1944-13546G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109803727 | ||||||
| chr5:109803732
|
G | T | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1944-13541G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109803732 | ||||||
| chr5:109803839
|
A | C | 28 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1944-13434A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109803839 | ||||||
| chr5:109803923
|
C | T | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(199): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1944-13350C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109803923 | ||||||
| chr5:109804073
|
C | G | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1944-13200C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109804073 | ||||||
| chr5:109804083
|
A | G | 7 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(4): Show | 7 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1944-13190A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109804083 | ||||||
| chr5:109804350
|
T | A | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1944-12923T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109804350 | ||||||
| chr5:109804394
|
G | A | 15 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1944-12879G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109804394 | ||||||
| chr5:109804405
|
C | G | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1944-12868C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109804405 | ||||||
| chr5:109804513
|
T | C | 30 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(27): Show | 31 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1944-12760T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109804513 | ||||||
| chr5:109804550
|
T | A | 15 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1944-12723T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109804550 | ||||||
| chr5:109804622
|
T | C | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1944-12651T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109804622 | ||||||
| chr5:109805006
|
C | T | 1 | a0001c0001t0005g0058 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1944-12267C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109805006 | ||||||
| chr5:109805167
|
C | T | 1 | a0001c0005t0003g0169 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1944-12106C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109805167 | ||||||
| chr5:109805304
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1944-11969C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109805304 | ||||||
| chr5:109805596
|
G | A | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1944-11677G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109805596 | ||||||
| chr5:109805719
|
C | T | 1 | a0001c0003t0019g0180 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1944-11554C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109805719 | ||||||
| chr5:109805779
|
A | T | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(195): Show | 203 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.1944-11494A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109805779 | ||||||
| chr5:109805820
|
G | A | 288 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(285): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1944-11453G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109805820 | ||||||
| chr5:109805826
|
T | G | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1944-11447T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109805826 | ||||||
| chr5:109805859
|
G | A | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1944-11414G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109805859 | ||||||
| chr5:109805922
|
C | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(88): Show | 94 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1944-11351C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109805922 | ||||||
| chr5:109805943
|
C | G | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1944-11330C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109805943 | ||||||
| chr5:109806116
|
T | G | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1944-11157T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109806116 | ||||||
| chr5:109806133
|
G | T | 2 | a0006c0012t0001g0028a0006c0012t0001g0029 | 2 | HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1944-11140G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109806133 | ||||||
| chr5:109806283
|
T | A | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1944-10990T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109806283 | ||||||
| chr5:109806337
|
A | C | 1 | a0001c0001t0001g0116 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1944-10936A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109806337 | ||||||
| chr5:109806509
|
A | T | 1 | a0002c0002t0002g0205 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1944-10764A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109806509 | ||||||
| chr5:109806683
|
A | T | 1 | a0001c0004t0013g0214 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1944-10590A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109806683 | ||||||
| chr5:109806724
|
T | G | 1 | a0001c0001t0005g0058 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1944-10549T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109806724 | ||||||
| chr5:109806740
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1944-10533A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109806740 | ||||||
| chr5:109806768
|
G | A | 1 | a0002c0002t0002g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1944-10505G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109806768 | ||||||
| chr5:109806777
|
A | C | 2 | a0001c0006t0006g0287a0001c0006t0006g0288 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1944-10496A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109806777 | ||||||
| chr5:109806797
|
T | G | 2 | a0001c0003t0003g0134a0001c0003t0003g0135 | 2 | HG00642.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1944-10476T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109806797 | ||||||
| chr5:109806852
|
G | A | 15 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1944-10421G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109806852 | ||||||
| chr5:109806956
|
A | G | 1 | a0001c0016t0020g0112 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1944-10317A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109806956 | ||||||
| chr5:109807130
|
A | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(103): Show | 109 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1944-10143A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109807130 | ||||||
| chr5:109807232
|
C | G | 11 | a0001c0001t0001g0039a0001c0001t0001g0056a0001c0001t0001g0083others(8): Show | 11 | HG00741.hp1 HG01074.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1944-10041C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109807232 | ||||||
| chr5:109807418
|
T | A | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1944-9855T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109807418 | ||||||
| chr5:109807623
|
C | T | 1 | a0002c0002t0011g0179 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1944-9650C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109807623 | ||||||
| chr5:109807685
|
C | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(86): Show | 92 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.1944-9588C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109807685 | ||||||
| chr5:109807721
|
A | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1944-9552A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109807721 | ||||||
| chr5:109807755
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1944-9518G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109807755 | ||||||
| chr5:109807788
|
A | G | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1944-9485A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109807788 | ||||||
| chr5:109807901
|
C | T | 121 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(118): Show | 123 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.1944-9372C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109807901 | ||||||
| chr5:109808137
|
G | A | 1 | a0001c0001t0005g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1944-9136G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109808137 | ||||||
| chr5:109808336
|
G | C | 25 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(22): Show | 26 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1944-8937G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109808336 | ||||||
| chr5:109808428
|
A | T | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1944-8845A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109808428 | ||||||
| chr5:109808702
|
AT | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(190): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1944-8552delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109808702 | |||||
| chr5:109808702
|
ATT | A | 7 | a0001c0001t0001g0092a0001c0001t0001g0290a0001c0005t0010g0014others(4): Show | 7 | HG01891.hp2 HG02040.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1944-8553_1944-855 others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109808702 | |||||
| chr5:109808846
|
C | T | 2 | a0002c0002t0002g0232a0002c0002t0009g0200 | 2 | NA18962.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1944-8427C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109808846 | ||||||
| chr5:109808922
|
C | T | 1 | a0001c0003t0003g0185 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1944-8351C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109808922 | ||||||
| chr5:109808927
|
T | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(104): Show | 110 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1944-8346T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109808927 | ||||||
| chr5:109808964
|
A | C | 1 | a0001c0006t0006g0172 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1944-8309A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109808964 | ||||||
| chr5:109809120
|
A | G | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG01167.hp2 HG01169.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1944-8153A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109809120 | ||||||
| chr5:109809300
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1944-7973G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109809300 | ||||||
| chr5:109809348
|
G | A | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1944-7925G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109809348 | ||||||
| chr5:109809453
|
C | T | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1944-7820C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109809453 | ||||||
| chr5:109809489
|
T | C | 121 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(118): Show | 123 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.1944-7784T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109809489 | ||||||
| chr5:109809780
|
T | C | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1944-7493T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109809780 | ||||||
| chr5:109809789
|
C | T | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1944-7484C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109809789 | ||||||
| chr5:109809802
|
G | T | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1944-7471G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109809802 | ||||||
| chr5:109809945
|
T | G | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1944-7328T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109809945 | ||||||
| chr5:109810105
|
T | C | 1 | a0001c0004t0004g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1944-7168T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109810105 | ||||||
| chr5:109810538
|
A | G | 1 | a0001c0005t0021g0262 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1944-6735A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109810538 | ||||||
| chr5:109810559
|
A | G | 1 | a0002c0002t0002g0243 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1944-6714A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109810559 | ||||||
| chr5:109810622
|
T | G | 1 | a0002c0002t0002g0225 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1944-6651T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109810622 | ||||||
| chr5:109810727
|
G | C | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1944-6546G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109810727 | ||||||
| chr5:109810803
|
T | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | NA18983.hp2 NA19080.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1944-6470T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109810803 | ||||||
| chr5:109810920
|
A | G | 1 | a0001c0004t0004g0048 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1944-6353A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109810920 | ||||||
| chr5:109810991
|
AT | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(216): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1944-6268delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109810991 | |||||
| chr5:109811051
|
T | G | 191 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(188): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1944-6222T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109811051 | ||||||
| chr5:109811074
|
C | T | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1944-6199C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109811074 | ||||||
| chr5:109811551
|
G | A | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1944-5722G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109811551 | ||||||
| chr5:109811552
|
ATTG | A | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1944-5718_1944-571 others(7): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109811552 | |||||
| chr5:109811573
|
C | CGT | 14 | a0001c0001t0001g0097a0001c0001t0001g0107a0001c0003t0003g0164others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1944-5667_1944-566 others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109811573 | |||||
| chr5:109811573
|
C | CGTGT | 8 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282others(5): Show | 8 | HG01192.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1944-5669_1944-566 others(8): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109811573 | |||||
| chr5:109811573
|
C | CGTGTGT | 3 | a0001c0005t0010g0019a0001c0005t0010g0020a0004c0008t0014g0021 | 3 | HG02027.hp1 HG03516.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.1944-5671_1944-566 others(10): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109811573 | |||||
| chr5:109811573
|
C | CGTGTGTG others(3): Show |
1 | a0001c0005t0021g0262 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1944-5675_1944-566 others(14): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109811573 | |||||
| chr5:109811573
|
CGT | C | 10 | a0001c0001t0001g0098a0001c0001t0005g0058a0001c0004t0015g0040others(7): Show | 10 | HG01109.hp2 HG02895.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.1944-5667_1944-566 others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109811573 | |||||
| chr5:109811573
|
CGTGTGT | C | 79 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(76): Show | 80 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.1944-5671_1944-566 others(10): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109811573 | |||||
| chr5:109811573
|
CGTGTGTG others(9): Show |
C | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1944-5681_1944-566 others(20): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109811573 | |||||
| chr5:109811600
|
G | C | 7 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(4): Show | 7 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1944-5673G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109811600 | ||||||
| chr5:109811623
|
T | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0104 | 2 | NA19080.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1944-5650T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109811623 | ||||||
| chr5:109812189
|
C | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1944-5084C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109812189 | ||||||
| chr5:109812319
|
T | C | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1944-4954T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109812319 | ||||||
| chr5:109812471
|
T | G | 1 | a0001c0001t0001g0063 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1944-4802T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109812471 | ||||||
| chr5:109812473
|
C | T | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(221): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1944-4800C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109812473 | ||||||
| chr5:109812547
|
C | T | 1 | a0002c0002t0002g0241 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1944-4726C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109812547 | ||||||
| chr5:109812570
|
A | C | 2 | a0001c0004t0004g0030a0001c0004t0004g0031 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1944-4703A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109812570 | ||||||
| chr5:109813016
|
T | A | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1944-4257T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109813016 | ||||||
| chr5:109813141
|
T | C | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1944-4132T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109813141 | ||||||
| chr5:109813241
|
G | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(103): Show | 109 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1944-4032G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109813241 | ||||||
| chr5:109813326
|
T | G | 6 | a0002c0002t0002g0189a0002c0002t0002g0236a0002c0002t0002g0239others(3): Show | 6 | HG00099.hp2 HG01934.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1944-3947T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109813326 | ||||||
| chr5:109813379
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1944-3894T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109813379 | ||||||
| chr5:109813705
|
A | G | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1944-3568A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109813705 | ||||||
| chr5:109813760
|
C | T | 1 | a0001c0003t0003g0129 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1944-3513C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109813760 | ||||||
| chr5:109813815
|
C | A | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1944-3458C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109813815 | ||||||
| chr5:109813997
|
G | T | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1944-3276G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109813997 | ||||||
| chr5:109814023
|
C | T | 11 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0005g0281others(8): Show | 11 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1944-3250C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109814023 | ||||||
| chr5:109814077
|
G | A | 3 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0018t0032g0084 | 3 | HG01891.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1944-3196G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109814077 | ||||||
| chr5:109814301
|
C | G | 1 | a0001c0004t0004g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1944-2972C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109814301 | ||||||
| chr5:109814340
|
A | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1944-2933A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109814340 | ||||||
| chr5:109814365
|
A | T | 1 | a0001c0003t0003g0027 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1944-2908A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109814365 | ||||||
| chr5:109814532
|
C | T | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(176): Show | 183 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.1944-2741C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109814532 | ||||||
| chr5:109814778
|
A | G | 1 | a0002c0002t0002g0229 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1944-2495A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109814778 | ||||||
| chr5:109814781
|
A | G | 1 | a0001c0001t0001g0003 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1944-2492A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109814781 | ||||||
| chr5:109815030
|
C | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(88): Show | 94 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1944-2243C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109815030 | ||||||
| chr5:109815089
|
T | A | 1 | a0001c0003t0003g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1944-2184T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109815089 | ||||||
| chr5:109815152
|
A | G | 1 | a0001c0005t0008g0010 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1944-2121A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109815152 | ||||||
| chr5:109815219
|
A | T | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1944-2054A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109815219 | ||||||
| chr5:109815274
|
G | A | 2 | a0001c0004t0004g0047a0001c0004t0004g0048 | 2 | HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1944-1999G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109815274 | ||||||
| chr5:109815372
|
C | T | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1944-1901C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109815372 | ||||||
| chr5:109815485
|
A | G | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1944-1788A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109815485 | ||||||
| chr5:109815507
|
A | G | 1 | a0003c0007t0001g0196 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1944-1766A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109815507 | ||||||
| chr5:109815586
|
A | G | 1 | a0001c0004t0013g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1944-1687A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109815586 | ||||||
| chr5:109815618
|
T | C | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1944-1655T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109815618 | ||||||
| chr5:109815737
|
A | G | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1944-1536A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109815737 | ||||||
| chr5:109815801
|
C | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1944-1472C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109815801 | ||||||
| chr5:109815864
|
C | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1944-1409C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109815864 | ||||||
| chr5:109815913
|
A | G | 2 | a0001c0006t0022g0035a0001c0009t0028g0008 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1944-1360A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109815913 | ||||||
| chr5:109815917
|
A | C | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1944-1356A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109815917 | ||||||
| chr5:109815955
|
C | G | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1944-1318C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109815955 | ||||||
| chr5:109816082
|
C | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1944-1191C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109816082 | ||||||
| chr5:109816140
|
A | T | 2 | a0002c0002t0009g0007a0002c0002t0009g0215 | 2 | HG00642.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1944-1133A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109816140 | ||||||
| chr5:109816212
|
C | T | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1944-1061C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109816212 | ||||||
| chr5:109816233
|
T | C | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(101): Show | 108 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.1944-1040T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109816233 | ||||||
| chr5:109816244
|
TA | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1944-1025delA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109816244 | |||||
| chr5:109816369
|
G | A | 1 | a0001c0001t0005g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1944-904G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109816369 | ||||||
| chr5:109816522
|
A | G | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1944-751A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109816522 | ||||||
| chr5:109816753
|
C | T | 1 | a0001c0003t0003g0167 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1944-520C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109816753 | ||||||
| chr5:109816784
|
G | T | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1944-489G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109816784 | ||||||
| chr5:109816880
|
T | C | 1 | a0001c0001t0005g0074 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1944-393T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109816880 | ||||||
| chr5:109816954
|
A | T | 1 | a0001c0001t0005g0058 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1944-319A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109816954 | ||||||
| chr5:109816989
|
A | G | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1944-284A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109816989 | ||||||
| chr5:109817105
|
G | T | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1944-168G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109817105 | ||||||
| chr5:109817172
|
A | ATATATGT others(23): Show |
2 | a0001c0004t0013g0214a0001c0004t0013g0282 | 2 | HG01192.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1944-72_1944-71ins others(30): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109817172 | |||||
| chr5:109817172
|
A | ATATATGT others(29): Show |
1 | a0001c0004t0013g0049 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1944-72_1944-71ins others(36): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109817172 | |||||
| chr5:109817172
|
ATATATG | A | 5 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0011t0016g0025others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1944-77_1944-72del others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109817172 | |||||
| chr5:109817172
|
ATATATGT others(5): Show |
A | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(182): Show | 190 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.1944-83_1944-72del others(12): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 109817172 | |||||
| chr5:109817196
|
G | A | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1944-77G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109817196 | ||||||
| chr5:109817206
|
A | G | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1944-67A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | chr5 | 109817206 | ||||||
| chr5:109817583
|
G | A | 1 | a0002c0002t0002g0221 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2109+145G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109817583 | ||||||
| chr5:109817670
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2109+232T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109817670 | ||||||
| chr5:109817708
|
T | C | 3 | a0001c0003t0003g0201a0001c0003t0003g0209a0001c0003t0003g0213 | 3 | HG01167.hp1 HG01943.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2109+270T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109817708 | ||||||
| chr5:109817723
|
C | T | 28 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(25): Show | 29 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2109+285C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109817723 | ||||||
| chr5:109818056
|
C | T | 1 | a0002c0002t0017g0276 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2109+618C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109818056 | ||||||
| chr5:109818062
|
T | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2109+624T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109818062 | ||||||
| chr5:109818161
|
A | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(104): Show | 111 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.2109+723A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109818161 | ||||||
| chr5:109818197
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2109+759A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109818197 | ||||||
| chr5:109818210
|
G | A | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.2109+772G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109818210 | ||||||
| chr5:109818213
|
G | A | 1 | a0002c0002t0002g0241 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2109+775G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109818213 | ||||||
| chr5:109818248
|
CTCCTGCC others(11): Show |
C | 1 | a0009c0015t0001g0075 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2109+812_2109+829d others(20): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr5 | 109818248 | |||||
| chr5:109818270
|
CTGGGATT others(5): Show |
C | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2109+833_2109+844d others(14): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109818270 | ||||||
| chr5:109818284
|
A | C | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2109+846A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109818284 | ||||||
| chr5:109818326
|
G | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(101): Show | 108 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.2109+888G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109818326 | ||||||
| chr5:109818328
|
G | C | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2109+890G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109818328 | ||||||
| chr5:109818602
|
T | C | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2110-1067T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109818602 | ||||||
| chr5:109818683
|
A | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(104): Show | 111 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.2110-986A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109818683 | ||||||
| chr5:109818749
|
A | C | 1 | a0009c0015t0001g0075 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2110-920A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109818749 | ||||||
| chr5:109819032
|
A | G | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2110-637A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109819032 | ||||||
| chr5:109819144
|
A | G | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2110-525A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109819144 | ||||||
| chr5:109819198
|
G | A | 2 | a0001c0001t0001g0055a0004c0008t0014g0021 | 2 | HG01256.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2110-471G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109819198 | ||||||
| chr5:109819248
|
A | AT | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2110-417dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr5 | 109819248 | |||||
| chr5:109819298
|
C | T | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.2110-371C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109819298 | ||||||
| chr5:109819507
|
A | G | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(224): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2110-162A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109819507 | ||||||
| chr5:109819508
|
T | G | 1 | a0009c0015t0001g0075 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2110-161T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109819508 | ||||||
| chr5:109819560
|
C | A | 1 | a0001c0011t0016g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2110-109C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 13/21 | chr5 | 109819560 | ||||||
| chr5:109819939
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2328+52A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 14/21 | chr5 | 109819939 | ||||||
| chr5:109819957
|
A | G | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.2328+70A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 14/21 | chr5 | 109819957 | ||||||
| chr5:109819986
|
A | G | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2328+99A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 14/21 | chr5 | 109819986 | ||||||
| chr5:109820001
|
T | C | 1 | a0009c0015t0001g0075 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2328+114T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 14/21 | chr5 | 109820001 | ||||||
| chr5:109820086
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(173): Show | 180 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.2329-134G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 14/21 | chr5 | 109820086 | ||||||
| chr5:109820136
|
A | T | 15 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.2329-84A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 14/21 | chr5 | 109820136 | ||||||
| chr5:109820205
|
T | A | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2329-15T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 14/21 | chr5 | 109820205 | ||||||
| chr5:109820348
|
T | A | 1 | a0009c0015t0001g0075 | 1 | NA18956.hp1 | splice_region_variant&intron_variant | LOW | c.2451+6T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109820348 | ||||||
| chr5:109820411
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2451+69G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109820411 | ||||||
| chr5:109820427
|
T | G | 1 | a0009c0015t0001g0075 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2451+85T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109820427 | ||||||
| chr5:109820483
|
A | G | 49 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0055others(46): Show | 51 | HG00639.hp1 HG01071.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.2451+141A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109820483 | ||||||
| chr5:109820519
|
A | G | 1 | a0001c0005t0035g0013 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2451+177A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109820519 | ||||||
| chr5:109820596
|
C | G | 8 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.2451+254C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109820596 | ||||||
| chr5:109820669
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2451+327G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109820669 | ||||||
| chr5:109820685
|
G | A | 1 | a0002c0002t0002g0255 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2451+343G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109820685 | ||||||
| chr5:109820864
|
G | T | 7 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(4): Show | 7 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2451+522G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109820864 | ||||||
| chr5:109820955
|
C | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(86): Show | 92 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.2451+613C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109820955 | ||||||
| chr5:109820960
|
G | A | 1 | a0002c0002t0027g0234 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2451+618G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109820960 | ||||||
| chr5:109821047
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2451+705G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109821047 | ||||||
| chr5:109821149
|
A | T | 1 | a0001c0001t0001g0119 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2451+807A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109821149 | ||||||
| chr5:109821190
|
C | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2451+848C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109821190 | ||||||
| chr5:109821224
|
A | G | 15 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.2451+882A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109821224 | ||||||
| chr5:109821230
|
A | G | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2451+888A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109821230 | ||||||
| chr5:109821410
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2451+1068A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109821410 | ||||||
| chr5:109821443
|
A | G | 1 | a0002c0002t0009g0200 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2451+1101A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109821443 | ||||||
| chr5:109821616
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2451+1274T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109821616 | ||||||
| chr5:109821678
|
G | A | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2451+1336G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109821678 | ||||||
| chr5:109821843
|
A | G | 81 | a0001c0003t0003g0139a0001c0009t0001g0208a0001c0009t0002g0227others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2451+1501A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109821843 | ||||||
| chr5:109821970
|
A | G | 82 | a0001c0003t0003g0139a0001c0006t0022g0035a0001c0009t0001g0208others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.2451+1628A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109821970 | ||||||
| chr5:109821997
|
T | A | 4 | a0002c0002t0002g0228a0002c0002t0002g0255a0002c0002t0024g0233others(1): Show | 4 | HG00597.hp2 NA18952.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.2451+1655T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109821997 | ||||||
| chr5:109822010
|
G | A | 1 | a0002c0002t0002g0248 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2451+1668G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109822010 | ||||||
| chr5:109822095
|
T | C | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.2452-1628T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109822095 | ||||||
| chr5:109822171
|
C | CT | 8 | a0001c0003t0003g0125a0001c0003t0003g0162a0001c0003t0003g0187others(5): Show | 8 | HG00597.hp1 HG01109.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.2452-1537dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr5 | 109822171 | |||||
| chr5:109822171
|
CT | C | 9 | a0001c0001t0001g0055a0001c0001t0001g0066a0001c0003t0003g0148others(6): Show | 9 | HG01069.hp2 HG01167.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.2452-1537delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr5 | 109822171 | |||||
| chr5:109822188
|
A | T | 1 | a0002c0002t0002g0242 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2452-1535A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109822188 | ||||||
| chr5:109822362
|
A | C | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(121): Show | 128 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.2452-1361A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109822362 | ||||||
| chr5:109822457
|
G | C | 3 | a0001c0003t0003g0130a0001c0003t0003g0132a0001c0003t0003g0133 | 3 | HG03491.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2452-1266G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109822457 | ||||||
| chr5:109822492
|
C | G | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2452-1231C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109822492 | ||||||
| chr5:109822741
|
G | A | 5 | a0001c0003t0003g0151a0001c0003t0003g0152a0001c0003t0003g0154others(2): Show | 5 | NA18945.hp2 NA18965.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.2452-982G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109822741 | ||||||
| chr5:109822751
|
C | T | 7 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(4): Show | 7 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2452-972C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109822751 | ||||||
| chr5:109822929
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2452-794G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109822929 | ||||||
| chr5:109823026
|
A | G | 1 | a0001c0003t0003g0127 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2452-697A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109823026 | ||||||
| chr5:109823134
|
A | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2452-589A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109823134 | ||||||
| chr5:109823395
|
C | G | 2 | a0001c0005t0008g0011a0001c0005t0008g0012 | 2 | HG00099.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.2452-328C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109823395 | ||||||
| chr5:109823608
|
A | G | 1 | a0010c0020t0003g0174 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2452-115A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109823608 | ||||||
| chr5:109823647
|
G | A | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.2452-76G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109823647 | ||||||
| chr5:109823705
|
A | G | 1 | a0001c0004t0004g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2452-18A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 15/21 | chr5 | 109823705 | ||||||
| chr5:109823867
|
A | T | 10 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(7): Show | 11 | HG01243.hp1 HG02280.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.2566+30A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109823867 | ||||||
| chr5:109823934
|
A | G | 1 | a0002c0002t0002g0224 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2566+97A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109823934 | ||||||
| chr5:109824016
|
G | A | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(224): Show | 233 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(230): Show |
intron_variant | MODIFIER | c.2566+179G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109824016 | ||||||
| chr5:109824022
|
A | G | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2566+185A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109824022 | ||||||
| chr5:109824123
|
A | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(103): Show | 110 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.2566+286A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109824123 | ||||||
| chr5:109824282
|
G | A | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2566+445G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109824282 | ||||||
| chr5:109824285
|
C | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2566+448C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109824285 | ||||||
| chr5:109824550
|
T | G | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2566+713T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109824550 | ||||||
| chr5:109824717
|
G | A | 4 | a0001c0004t0004g0001a0001c0004t0004g0044a0001c0004t0004g0045others(1): Show | 5 | HG01243.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2566+880G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109824717 | ||||||
| chr5:109824825
|
A | C | 1 | a0001c0004t0013g0214 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2566+988A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109824825 | ||||||
| chr5:109825204
|
G | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG00741.hp1 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2566+1367G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109825204 | ||||||
| chr5:109825239
|
C | A | 40 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(37): Show | 41 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.2566+1402C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109825239 | ||||||
| chr5:109825391
|
G | C | 4 | a0002c0002t0002g0265a0002c0002t0002g0266a0002c0002t0002g0267others(1): Show | 4 | HG02738.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.2566+1554G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109825391 | ||||||
| chr5:109825900
|
C | CT | 31 | a0001c0001t0001g0066a0001c0001t0001g0080a0001c0001t0001g0081others(28): Show | 31 | HG00735.hp2 HG01255.hp2 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.2566+2089dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109825900 | |||||
| chr5:109825900
|
CT | C | 13 | a0001c0001t0001g0094a0001c0004t0004g0001a0001c0004t0004g0042others(10): Show | 14 | HG00099.hp1 HG02280.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.2566+2089delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109825900 | |||||
| chr5:109825900
|
CTT | C | 18 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(15): Show | 18 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.2566+2088_2566+208 others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109825900 | |||||
| chr5:109825900
|
CTTT | C | 79 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0009t0001g0208others(76): Show | 80 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.2566+2087_2566+208 others(7): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109825900 | |||||
| chr5:109825926
|
T | G | 2 | a0002c0002t0002g0258a0002c0002t0002g0259 | 2 | HG01433.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2566+2089T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109825926 | ||||||
| chr5:109826054
|
C | T | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.2566+2217C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109826054 | ||||||
| chr5:109826125
|
C | T | 13 | a0001c0004t0036g0024a0001c0006t0002g0278a0001c0006t0002g0279others(10): Show | 13 | HG01891.hp2 HG02451.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.2566+2288C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109826125 | ||||||
| chr5:109826192
|
C | G | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2566+2355C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109826192 | ||||||
| chr5:109826222
|
T | G | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2566+2385T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109826222 | ||||||
| chr5:109826262
|
G | A | 37 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(34): Show | 38 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.2566+2425G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109826262 | ||||||
| chr5:109826325
|
G | A | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2566+2488G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109826325 | ||||||
| chr5:109826421
|
C | T | 2 | a0002c0002t0009g0007a0002c0002t0009g0215 | 2 | HG00642.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2566+2584C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109826421 | ||||||
| chr5:109826515
|
G | A | 40 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(37): Show | 41 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.2566+2678G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109826515 | ||||||
| chr5:109826533
|
C | G | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2566+2696C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109826533 | ||||||
| chr5:109826536
|
T | G | 1 | a0001c0003t0003g0138 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2566+2699T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109826536 | ||||||
| chr5:109826615
|
C | T | 1 | a0002c0002t0002g0242 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2566+2778C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109826615 | ||||||
| chr5:109826979
|
A | G | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2566+3142A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109826979 | ||||||
| chr5:109827108
|
C | T | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2566+3271C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109827108 | ||||||
| chr5:109827183
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2566+3346G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109827183 | ||||||
| chr5:109827350
|
C | G | 1 | a0002c0002t0002g0248 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2566+3513C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109827350 | ||||||
| chr5:109827484
|
A | G | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2566+3647A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109827484 | ||||||
| chr5:109827554
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2566+3717A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109827554 | ||||||
| chr5:109827645
|
G | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(88): Show | 94 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.2566+3808G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109827645 | ||||||
| chr5:109827720
|
G | A | 1 | a0002c0017t0002g0101 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2566+3883G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109827720 | ||||||
| chr5:109828013
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2566+4176G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109828013 | ||||||
| chr5:109828061
|
C | T | 1 | a0002c0002t0002g0206 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2566+4224C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109828061 | ||||||
| chr5:109828062
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2566+4225G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109828062 | ||||||
| chr5:109828104
|
C | CA | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.2566+4281dupA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109828104 | |||||
| chr5:109828104
|
CA | C | 42 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(39): Show | 43 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.2566+4281delA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109828104 | |||||
| chr5:109828122
|
AAAAAG | A | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2566+4290_2566+429 others(9): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109828122 | |||||
| chr5:109828367
|
A | G | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(239): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.2566+4530A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109828367 | ||||||
| chr5:109828377
|
T | G | 1 | a0002c0002t0002g0221 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2566+4540T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109828377 | ||||||
| chr5:109828435
|
C | T | 1 | a0002c0002t0002g0241 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2566+4598C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109828435 | ||||||
| chr5:109828774
|
C | G | 1 | a0001c0006t0006g0172 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2566+4937C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109828774 | ||||||
| chr5:109829065
|
CTA | C | 23 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(20): Show | 24 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.2566+5230_2566+523 others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109829065 | |||||
| chr5:109829185
|
C | T | 1 | a0002c0002t0002g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2566+5348C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109829185 | ||||||
| chr5:109829274
|
T | C | 23 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(20): Show | 24 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.2566+5437T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109829274 | ||||||
| chr5:109829464
|
C | T | 1 | a0001c0004t0029g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2566+5627C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109829464 | ||||||
| chr5:109829730
|
C | T | 4 | a0001c0001t0001g0039a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG00741.hp1 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2566+5893C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109829730 | ||||||
| chr5:109830076
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2566+6239A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109830076 | ||||||
| chr5:109830083
|
A | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(105): Show | 112 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.2566+6246A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109830083 | ||||||
| chr5:109830244
|
G | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(216): Show | 225 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(222): Show |
intron_variant | MODIFIER | c.2566+6407G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109830244 | ||||||
| chr5:109830407
|
T | C | 7 | a0001c0003t0003g0131a0001c0003t0003g0134a0001c0003t0003g0135others(4): Show | 7 | HG00642.hp2 HG01074.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.2566+6570T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109830407 | ||||||
| chr5:109830486
|
T | G | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(185): Show | 193 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.2566+6649T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109830486 | ||||||
| chr5:109830640
|
G | A | 1 | a0001c0004t0015g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2566+6803G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109830640 | ||||||
| chr5:109830643
|
A | G | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2566+6806A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109830643 | ||||||
| chr5:109830822
|
C | T | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(224): Show | 233 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(230): Show |
intron_variant | MODIFIER | c.2566+6985C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109830822 | ||||||
| chr5:109830827
|
C | T | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(101): Show | 108 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.2566+6990C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109830827 | ||||||
| chr5:109830842
|
G | A | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2566+7005G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109830842 | ||||||
| chr5:109831140
|
A | T | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2566+7303A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109831140 | ||||||
| chr5:109831188
|
A | C | 4 | a0001c0005t0008g0009a0001c0005t0008g0010a0001c0005t0008g0016others(1): Show | 4 | HG00140.hp1 HG00639.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.2566+7351A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109831188 | ||||||
| chr5:109831249
|
A | G | 80 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2566+7412A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109831249 | ||||||
| chr5:109831318
|
C | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2566+7481C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109831318 | ||||||
| chr5:109831347
|
T | C | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2566+7510T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109831347 | ||||||
| chr5:109831500
|
T | C | 1 | a0002c0002t0002g0273 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2566+7663T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109831500 | ||||||
| chr5:109831579
|
A | T | 4 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282others(1): Show | 4 | HG01192.hp1 HG03017.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2566+7742A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109831579 | ||||||
| chr5:109831580
|
T | C | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2566+7743T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109831580 | ||||||
| chr5:109831601
|
A | G | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2566+7764A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109831601 | ||||||
| chr5:109831670
|
C | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2566+7833C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109831670 | ||||||
| chr5:109831804
|
C | CGTGT | 8 | a0001c0004t0004g0030a0001c0004t0004g0031a0001c0004t0004g0033others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.2566+7967_2566+796 others(8): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109831804 | ||||||
| chr5:109831804
|
CAT | C | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0005g0111 | 3 | HG01123.hp2 HG01346.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2566+7968_2566+796 others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109831804 | ||||||
| chr5:109831805
|
A | ATG | 14 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0004t0013g0049others(11): Show | 14 | HG01192.hp1 HG02647.hp2 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.2566+7994_2566+799 others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109831805 | |||||
| chr5:109831805
|
A | G | 23 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(20): Show | 24 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.2566+7968A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109831805 | ||||||
| chr5:109831805
|
ATG | A | 30 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(27): Show | 31 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.2566+7994_2566+799 others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109831805 | |||||
| chr5:109831901
|
T | G | 10 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(7): Show | 11 | HG01243.hp1 HG02280.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.2566+8064T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109831901 | ||||||
| chr5:109831905
|
AATT | A | 8 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0011t0016g0025others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2566+8075_2566+807 others(7): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109831905 | |||||
| chr5:109832083
|
T | A | 1 | a0002c0002t0002g0220 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2566+8246T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832083 | ||||||
| chr5:109832151
|
AAGG | A | 6 | a0002c0002t0002g0219a0002c0002t0002g0222a0002c0002t0002g0226others(3): Show | 6 | HG01934.hp1 HG03491.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.2566+8317_2566+831 others(7): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109832151 | |||||
| chr5:109832154
|
G | T | 74 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(71): Show | 75 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.2566+8317G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832154 | ||||||
| chr5:109832155
|
A | T | 74 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(71): Show | 75 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.2566+8318A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832155 | ||||||
| chr5:109832156
|
G | C | 1 | a0002c0002t0002g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2566+8319G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832156 | ||||||
| chr5:109832156
|
G | T | 73 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(70): Show | 74 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.2566+8319G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832156 | ||||||
| chr5:109832157
|
T | TC | 9 | a0002c0002t0002g0254a0002c0002t0002g0255a0002c0002t0002g0258others(6): Show | 9 | HG00597.hp2 HG01433.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2566+8320_2566+832 others(5): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832157 | ||||||
| chr5:109832158
|
T | C | 64 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(61): Show | 65 | HG00099.hp2 HG00438.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.2566+8321T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832158 | ||||||
| chr5:109832161
|
C | CT | 12 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0092others(9): Show | 12 | HG01071.hp1 HG01109.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.2566+8349dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109832161 | |||||
| chr5:109832161
|
C | CTT | 6 | a0002c0002t0002g0219a0002c0002t0002g0222a0002c0002t0002g0226others(3): Show | 6 | HG01934.hp1 HG03491.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.2566+8348_2566+834 others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109832161 | |||||
| chr5:109832161
|
C | T | 74 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(71): Show | 75 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.2566+8324C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832161 | ||||||
| chr5:109832161
|
CT | C | 16 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0072others(13): Show | 16 | HG01074.hp1 HG01081.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.2566+8349delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109832161 | |||||
| chr5:109832161
|
CTT | C | 12 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282others(9): Show | 12 | HG01192.hp1 HG02055.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.2566+8348_2566+834 others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109832161 | |||||
| chr5:109832253
|
T | C | 1 | a0001c0004t0013g0049 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2566+8416T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832253 | ||||||
| chr5:109832428
|
C | T | 15 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0005g0281others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2566+8591C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832428 | ||||||
| chr5:109832432
|
C | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0005g0111 | 3 | HG01123.hp2 HG01346.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2566+8595C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832432 | ||||||
| chr5:109832525
|
A | G | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.2566+8688A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832525 | ||||||
| chr5:109832538
|
G | A | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2566+8701G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832538 | ||||||
| chr5:109832565
|
T | A | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2566+8728T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832565 | ||||||
| chr5:109832655
|
G | A | 1 | a0002c0002t0002g0273 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2566+8818G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832655 | ||||||
| chr5:109832667
|
C | T | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2566+8830C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832667 | ||||||
| chr5:109832724
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2566+8887G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832724 | ||||||
| chr5:109832738
|
C | T | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2566+8901C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832738 | ||||||
| chr5:109832746
|
T | C | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(209): Show | 217 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(214): Show |
intron_variant | MODIFIER | c.2566+8909T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832746 | ||||||
| chr5:109832751
|
C | T | 23 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(20): Show | 24 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.2566+8914C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832751 | ||||||
| chr5:109832776
|
C | T | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2566+8939C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832776 | ||||||
| chr5:109832789
|
G | A | 13 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0005g0281others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2566+8952G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832789 | ||||||
| chr5:109832792
|
C | T | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2566+8955C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832792 | ||||||
| chr5:109832834
|
GGGGGCGG others(33): Show |
G | 13 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0005g0281others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2566+9032_2566+907 others(44): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109832834 | |||||
| chr5:109832851
|
G | A | 1 | a0003c0007t0001g0197 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2566+9014G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832851 | ||||||
| chr5:109832855
|
G | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(196): Show | 204 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.2566+9018G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832855 | ||||||
| chr5:109832856
|
G | C | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(196): Show | 204 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.2566+9019G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832856 | ||||||
| chr5:109832857
|
G | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(196): Show | 204 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.2566+9020G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832857 | ||||||
| chr5:109832880
|
G | A | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.2566+9043G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832880 | ||||||
| chr5:109832930
|
A | C | 5 | a0001c0003t0003g0027a0001c0003t0003g0143a0001c0003t0003g0145others(2): Show | 5 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.2566+9093A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832930 | ||||||
| chr5:109832977
|
C | T | 6 | a0001c0003t0007g0050a0001c0003t0007g0136a0001c0003t0007g0140others(3): Show | 6 | HG01106.hp2 HG01168.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.2566+9140C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109832977 | ||||||
| chr5:109833004
|
G | T | 23 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(20): Show | 24 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.2566+9167G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833004 | ||||||
| chr5:109833067
|
A | G | 1 | a0002c0002t0002g0243 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2566+9230A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833067 | ||||||
| chr5:109833089
|
C | T | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2567-9239C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833089 | ||||||
| chr5:109833103
|
C | G | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2567-9225C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833103 | ||||||
| chr5:109833142
|
C | T | 123 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(120): Show | 125 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.2567-9186C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833142 | ||||||
| chr5:109833172
|
C | T | 6 | a0001c0006t0006g0038a0001c0006t0006g0172a0001c0006t0006g0285others(3): Show | 6 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2567-9156C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833172 | ||||||
| chr5:109833191
|
C | CG | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2567-9135dupG | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109833191 | |||||
| chr5:109833191
|
C | T | 1 | a0001c0003t0003g0148 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2567-9137C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833191 | ||||||
| chr5:109833226
|
T | C | 23 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(20): Show | 24 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.2567-9102T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833226 | ||||||
| chr5:109833228
|
G | A | 5 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0011t0016g0025others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2567-9100G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833228 | ||||||
| chr5:109833254
|
T | C | 1 | a0002c0002t0002g0254 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2567-9074T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833254 | ||||||
| chr5:109833319
|
G | A | 8 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.2567-9009G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833319 | ||||||
| chr5:109833354
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2567-8974C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833354 | ||||||
| chr5:109833496
|
C | T | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2567-8832C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833496 | ||||||
| chr5:109833542
|
C | T | 13 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0005g0281others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2567-8786C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833542 | ||||||
| chr5:109833562
|
C | T | 5 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0011t0016g0025others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2567-8766C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833562 | ||||||
| chr5:109833566
|
A | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2567-8762A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833566 | ||||||
| chr5:109833655
|
C | T | 1 | a0001c0003t0003g0185 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2567-8673C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833655 | ||||||
| chr5:109833689
|
TGGGGAGG others(5): Show |
T | 1 | a0001c0001t0005g0074 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2567-8626_2567-861 others(16): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109833689 | |||||
| chr5:109833700
|
A | G | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2567-8628A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833700 | ||||||
| chr5:109833783
|
C | A | 5 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0011t0016g0025others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2567-8545C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109833783 | ||||||
| chr5:109834433
|
TA | T | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(221): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.2567-7885delA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109834433 | |||||
| chr5:109834444
|
C | A | 3 | a0001c0003t0007g0140a0001c0003t0007g0141a0001c0016t0020g0112 | 3 | HG01168.hp2 HG01515.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2567-7884C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109834444 | ||||||
| chr5:109834532
|
A | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2567-7796A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109834532 | ||||||
| chr5:109834584
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2567-7744G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109834584 | ||||||
| chr5:109834760
|
A | G | 23 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(20): Show | 24 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.2567-7568A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109834760 | ||||||
| chr5:109834818
|
A | G | 1 | a0001c0011t0016g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2567-7510A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109834818 | ||||||
| chr5:109834883
|
G | A | 1 | a0002c0002t0002g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2567-7445G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109834883 | ||||||
| chr5:109834883
|
G | C | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2567-7445G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109834883 | ||||||
| chr5:109835024
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2567-7304G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109835024 | ||||||
| chr5:109835471
|
T | C | 23 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(20): Show | 24 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.2567-6857T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109835471 | ||||||
| chr5:109835683
|
C | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2567-6645C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109835683 | ||||||
| chr5:109835705
|
C | T | 23 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(20): Show | 24 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.2567-6623C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109835705 | ||||||
| chr5:109835742
|
G | A | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2567-6586G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109835742 | ||||||
| chr5:109835747
|
G | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(196): Show | 204 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.2567-6581G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109835747 | ||||||
| chr5:109835919
|
G | T | 1 | a0001c0004t0033g0032 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2567-6409G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109835919 | ||||||
| chr5:109835972
|
A | G | 5 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0011t0016g0025others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2567-6356A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109835972 | ||||||
| chr5:109836115
|
A | G | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2567-6213A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109836115 | ||||||
| chr5:109836128
|
C | T | 1 | a0001c0001t0005g0058 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2567-6200C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109836128 | ||||||
| chr5:109836133
|
G | A | 1 | a0002c0002t0025g0263 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2567-6195G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109836133 | ||||||
| chr5:109836287
|
G | GT | 23 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(20): Show | 24 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.2567-6032dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109836287 | |||||
| chr5:109836296
|
T | A | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(167): Show | 174 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.2567-6032T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109836296 | ||||||
| chr5:109836332
|
G | A | 2 | a0001c0006t0006g0287a0001c0006t0006g0288 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2567-5996G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109836332 | ||||||
| chr5:109836368
|
G | A | 7 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(4): Show | 7 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2567-5960G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109836368 | ||||||
| chr5:109836400
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2567-5928G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109836400 | ||||||
| chr5:109836474
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(86): Show | 92 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.2567-5854G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109836474 | ||||||
| chr5:109836631
|
C | T | 1 | a0002c0002t0002g0264 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2567-5697C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109836631 | ||||||
| chr5:109836647
|
C | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(86): Show | 92 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.2567-5681C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109836647 | ||||||
| chr5:109836804
|
C | G | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2567-5524C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109836804 | ||||||
| chr5:109836856
|
G | A | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(218): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.2567-5472G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109836856 | ||||||
| chr5:109836867
|
G | A | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.2567-5461G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109836867 | ||||||
| chr5:109836986
|
C | G | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2567-5342C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109836986 | ||||||
| chr5:109837038
|
T | C | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2567-5290T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109837038 | ||||||
| chr5:109837398
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2567-4930A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109837398 | ||||||
| chr5:109837712
|
A | G | 1 | a0003c0007t0001g0198 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2567-4616A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109837712 | ||||||
| chr5:109837715
|
C | T | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2567-4613C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109837715 | ||||||
| chr5:109837796
|
C | T | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2567-4532C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109837796 | ||||||
| chr5:109837814
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2567-4514G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109837814 | ||||||
| chr5:109838005
|
G | C | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2567-4323G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109838005 | ||||||
| chr5:109838044
|
A | G | 1 | a0002c0002t0002g0178 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2567-4284A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109838044 | ||||||
| chr5:109838059
|
TA | T | 20 | a0001c0001t0001g0114a0001c0004t0013g0049a0001c0004t0013g0214others(17): Show | 20 | HG01192.hp1 HG01891.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.2567-4255delA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109838059 | |||||
| chr5:109838214
|
A | G | 14 | a0001c0003t0003g0126a0001c0003t0003g0147a0001c0003t0003g0148others(11): Show | 15 | NA18942.hp2 NA18945.hp2 NA18947.hp1 others(12): Show |
intron_variant | MODIFIER | c.2567-4114A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109838214 | ||||||
| chr5:109838428
|
A | G | 1 | a0002c0002t0002g0241 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2567-3900A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109838428 | ||||||
| chr5:109838655
|
C | T | 1 | a0001c0005t0010g0014 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2567-3673C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109838655 | ||||||
| chr5:109838764
|
T | A | 1 | a0001c0003t0003g0127 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2567-3564T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109838764 | ||||||
| chr5:109839086
|
A | AAAAACCC others(104): Show |
1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2567-3228_2567-322 others(115): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109839086 | |||||
| chr5:109839466
|
T | C | 23 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(20): Show | 24 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.2567-2862T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109839466 | ||||||
| chr5:109839483
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2567-2845G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109839483 | ||||||
| chr5:109839510
|
TA | T | 81 | a0001c0001t0001g0063a0001c0009t0001g0208a0001c0009t0002g0227others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2567-2805delA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109839510 | |||||
| chr5:109839567
|
C | T | 10 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0042others(7): Show | 11 | HG01243.hp1 HG02280.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.2567-2761C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109839567 | ||||||
| chr5:109839647
|
C | CT | 13 | a0001c0001t0001g0039a0001c0001t0001g0078a0001c0001t0001g0120others(10): Show | 13 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2567-2680dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109839647 | |||||
| chr5:109839648
|
TC | T | 80 | a0001c0001t0001g0104a0001c0001t0001g0113a0001c0009t0001g0208others(77): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2567-2679delC | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109839648 | ||||||
| chr5:109839649
|
C | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(115): Show | 122 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.2567-2679C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109839649 | ||||||
| chr5:109839669
|
T | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2567-2659T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109839669 | ||||||
| chr5:109839669
|
TA | T | 6 | a0001c0006t0006g0038a0001c0006t0006g0172a0001c0006t0006g0285others(3): Show | 6 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2567-2656delA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109839669 | |||||
| chr5:109839707
|
A | G | 2 | a0002c0002t0002g0232a0002c0002t0009g0200 | 2 | NA18962.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.2567-2621A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109839707 | ||||||
| chr5:109839780
|
G | A | 1 | a0001c0006t0006g0172 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2567-2548G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109839780 | ||||||
| chr5:109839922
|
A | T | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(209): Show | 217 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(214): Show |
intron_variant | MODIFIER | c.2567-2406A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109839922 | ||||||
| chr5:109839932
|
T | C | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2567-2396T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109839932 | ||||||
| chr5:109839934
|
CT | C | 10 | a0001c0001t0001g0072a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01069.hp2 HG01167.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.2567-2379delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 109839934 | |||||
| chr5:109839992
|
A | G | 4 | a0001c0001t0001g0039a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG00741.hp1 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2567-2336A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109839992 | ||||||
| chr5:109840139
|
T | C | 1 | a0002c0002t0002g0242 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2567-2189T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109840139 | ||||||
| chr5:109840373
|
G | A | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2567-1955G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109840373 | ||||||
| chr5:109840380
|
C | T | 3 | a0001c0003t0003g0201a0001c0003t0003g0209a0001c0003t0003g0213 | 3 | HG01167.hp1 HG01943.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2567-1948C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109840380 | ||||||
| chr5:109840388
|
A | G | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2567-1940A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109840388 | ||||||
| chr5:109840476
|
C | T | 1 | a0002c0002t0002g0225 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2567-1852C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109840476 | ||||||
| chr5:109840569
|
C | G | 1 | a0001c0006t0002g0278 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2567-1759C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109840569 | ||||||
| chr5:109840638
|
C | T | 1 | a0001c0003t0003g0128 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2567-1690C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109840638 | ||||||
| chr5:109840743
|
G | A | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2567-1585G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109840743 | ||||||
| chr5:109840755
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2567-1573G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109840755 | ||||||
| chr5:109840857
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | NA18983.hp2 NA19080.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2567-1471C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109840857 | ||||||
| chr5:109841177
|
A | G | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2567-1151A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109841177 | ||||||
| chr5:109841195
|
C | A | 1 | a0001c0003t0019g0180 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2567-1133C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109841195 | ||||||
| chr5:109841522
|
G | A | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2567-806G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109841522 | ||||||
| chr5:109841537
|
A | G | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2567-791A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109841537 | ||||||
| chr5:109841677
|
C | T | 122 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(119): Show | 124 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.2567-651C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109841677 | ||||||
| chr5:109841704
|
C | T | 7 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(4): Show | 7 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2567-624C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109841704 | ||||||
| chr5:109842075
|
C | G | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2567-253C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109842075 | ||||||
| chr5:109842090
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0081 | 2 | HG02055.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2567-238C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109842090 | ||||||
| chr5:109842114
|
A | T | 13 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0005g0281others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2567-214A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109842114 | ||||||
| chr5:109842173
|
T | G | 1 | a0002c0002t0002g0237 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2567-155T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109842173 | ||||||
| chr5:109842223
|
A | G | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2567-105A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109842223 | ||||||
| chr5:109842319
|
T | A | 8 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0067others(5): Show | 8 | NA18952.hp1 NA18956.hp1 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.2567-9T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 16/21 | chr5 | 109842319 | ||||||
| chr5:109842502
|
G | A | 1 | a0001c0001t0005g0099 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2700+41G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109842502 | ||||||
| chr5:109842516
|
T | C | 3 | a0001c0003t0003g0201a0001c0003t0003g0209a0001c0003t0003g0213 | 3 | HG01167.hp1 HG01943.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2700+55T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109842516 | ||||||
| chr5:109842615
|
G | A | 78 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(75): Show | 79 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.2700+154G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109842615 | ||||||
| chr5:109842676
|
AT | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(85): Show | 91 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.2700+218delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 109842676 | |||||
| chr5:109842806
|
G | GT | 24 | a0001c0001t0001g0078a0001c0001t0001g0113a0001c0003t0003g0125others(21): Show | 24 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.2700+362dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 109842806 | |||||
| chr5:109842806
|
G | GTTTTGTT others(6): Show |
1 | a0002c0002t0002g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2700+349_2700+350i others(15): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 109842806 | |||||
| chr5:109842806
|
G | GTTTTTTT others(4): Show |
1 | a0001c0011t0016g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2700+352_2700+362d others(13): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 109842806 | |||||
| chr5:109842806
|
G | GTTTTTTT others(5): Show |
4 | a0001c0004t0036g0024a0001c0011t0016g0026a0002c0002t0002g0203others(1): Show | 4 | HG02055.hp1 HG02293.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2700+351_2700+362d others(14): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 109842806 | |||||
| chr5:109842806
|
G | GTTTTTTT others(6): Show |
44 | a0001c0004t0015g0040a0001c0009t0001g0208a0001c0009t0002g0227others(41): Show | 44 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.2700+350_2700+362d others(15): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 109842806 | |||||
| chr5:109842806
|
G | GTTTTTTT others(7): Show |
39 | a0001c0004t0004g0042a0001c0004t0004g0051a0001c0004t0004g0053others(36): Show | 40 | HG00438.hp2 HG00609.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.2700+349_2700+362d others(16): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 109842806 | |||||
| chr5:109842806
|
G | GTTTTTTT others(8): Show |
7 | a0001c0004t0004g0001a0001c0004t0004g0041a0001c0004t0004g0045others(4): Show | 8 | HG01243.hp1 HG02280.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.2700+348_2700+362d others(17): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 109842806 | |||||
| chr5:109842806
|
G | GTTTTTTT others(9): Show |
11 | a0001c0004t0004g0030a0001c0004t0004g0033a0001c0004t0004g0043others(8): Show | 11 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.2700+347_2700+362d others(18): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 109842806 | |||||
| chr5:109842806
|
G | GTTTTTTT others(10): Show |
6 | a0001c0004t0004g0031a0001c0004t0004g0034a0001c0004t0004g0036others(3): Show | 6 | HG01106.hp1 HG01169.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.2700+346_2700+362d others(19): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 109842806 | |||||
| chr5:109842806
|
G | GTTTTTTT others(11): Show |
2 | a0001c0004t0013g0049a0001c0006t0006g0287 | 2 | HG02897.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.2700+362_2700+363i others(20): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 109842806 | |||||
| chr5:109842806
|
G | GTTTTTTT others(12): Show |
4 | a0001c0006t0006g0285a0001c0006t0006g0288a0001c0006t0022g0035others(1): Show | 4 | HG02895.hp1 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2700+362_2700+363i others(21): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 109842806 | |||||
| chr5:109842806
|
G | GTTTTTTT others(13): Show |
1 | a0001c0006t0006g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2700+362_2700+363i others(22): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 109842806 | |||||
| chr5:109842806
|
G | GTTTTTTT others(22): Show |
1 | a0001c0004t0013g0214 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2700+362_2700+363i others(31): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 109842806 | |||||
| chr5:109842806
|
G | GTTTTTTT others(26): Show |
1 | a0001c0004t0013g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2700+362_2700+363i others(35): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 109842806 | |||||
| chr5:109842836
|
C | T | 1 | a0001c0004t0029g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2700+375C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109842836 | ||||||
| chr5:109842987
|
G | A | 1 | a0002c0002t0002g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2700+526G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109842987 | ||||||
| chr5:109843058
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(85): Show | 91 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.2700+597G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109843058 | ||||||
| chr5:109843083
|
G | A | 10 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(7): Show | 10 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2700+622G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109843083 | ||||||
| chr5:109843086
|
A | C | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2700+625A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109843086 | ||||||
| chr5:109843101
|
C | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2700+640C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109843101 | ||||||
| chr5:109843377
|
C | T | 1 | a0001c0003t0003g0157 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2700+916C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109843377 | ||||||
| chr5:109843539
|
C | A | 78 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(75): Show | 79 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.2700+1078C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109843539 | ||||||
| chr5:109843765
|
C | T | 1 | a0002c0002t0002g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2700+1304C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109843765 | ||||||
| chr5:109843826
|
G | T | 1 | a0002c0002t0002g0271 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2700+1365G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109843826 | ||||||
| chr5:109843870
|
T | C | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2700+1409T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109843870 | ||||||
| chr5:109844017
|
CA | C | 7 | a0001c0006t0005g0281a0001c0006t0006g0038a0001c0006t0006g0172others(4): Show | 7 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2700+1557delA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109844017 | ||||||
| chr5:109844047
|
C | T | 9 | a0001c0001t0001g0039a0001c0001t0001g0083a0001c0001t0001g0106others(6): Show | 9 | HG00741.hp1 HG01074.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2700+1586C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109844047 | ||||||
| chr5:109844056
|
C | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(100): Show | 107 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.2700+1595C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109844056 | ||||||
| chr5:109844083
|
C | A | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2700+1622C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109844083 | ||||||
| chr5:109844319
|
T | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0104 | 2 | NA19080.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2701-1546T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109844319 | ||||||
| chr5:109844320
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(100): Show | 107 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.2701-1545A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109844320 | ||||||
| chr5:109844330
|
C | T | 3 | a0001c0003t0003g0201a0001c0003t0003g0209a0001c0003t0003g0213 | 3 | HG01167.hp1 HG01943.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2701-1535C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109844330 | ||||||
| chr5:109844380
|
C | T | 1 | a0002c0002t0002g0289 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2701-1485C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109844380 | ||||||
| chr5:109844449
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2701-1416A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109844449 | ||||||
| chr5:109844762
|
G | A | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(210): Show | 219 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(216): Show |
intron_variant | MODIFIER | c.2701-1103G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109844762 | ||||||
| chr5:109844780
|
G | T | 1 | a0001c0009t0002g0227 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2701-1085G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109844780 | ||||||
| chr5:109844993
|
G | A | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.2701-872G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109844993 | ||||||
| chr5:109845116
|
A | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(210): Show | 219 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(216): Show |
intron_variant | MODIFIER | c.2701-749A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109845116 | ||||||
| chr5:109845147
|
G | A | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2701-718G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109845147 | ||||||
| chr5:109845205
|
A | C | 21 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(18): Show | 22 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.2701-660A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109845205 | ||||||
| chr5:109845302
|
G | A | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2701-563G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109845302 | ||||||
| chr5:109845322
|
T | C | 1 | a0002c0002t0002g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2701-543T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109845322 | ||||||
| chr5:109845390
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG02145.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2701-475A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109845390 | ||||||
| chr5:109845686
|
C | G | 82 | a0001c0009t0001g0208a0001c0009t0002g0227a0001c0009t0028g0008others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.2701-179C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109845686 | ||||||
| chr5:109845732
|
A | T | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.2701-133A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 17/21 | chr5 | 109845732 | ||||||
| chr5:109846079
|
A | G | 1 | a0001c0003t0003g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2842+73A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 18/21 | chr5 | 109846079 | ||||||
| chr5:109846112
|
C | T | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2842+106C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 18/21 | chr5 | 109846112 | ||||||
| chr5:109846398
|
C | T | 1 | a0007c0014t0002g0193 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2842+392C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 18/21 | chr5 | 109846398 | ||||||
| chr5:109846495
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0100others(1): Show | 5 | HG01361.hp1 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.2842+489G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 18/21 | chr5 | 109846495 | ||||||
| chr5:109846885
|
T | C | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(223): Show | 232 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(229): Show |
intron_variant | MODIFIER | c.2843-772T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 18/21 | chr5 | 109846885 | ||||||
| chr5:109846946
|
C | T | 1 | a0001c0003t0003g0135 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2843-711C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 18/21 | chr5 | 109846946 | ||||||
| chr5:109846998
|
TA | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(100): Show | 107 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.2843-656delA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr5 | 109846998 | |||||
| chr5:109847077
|
C | T | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(210): Show | 219 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(216): Show |
intron_variant | MODIFIER | c.2843-580C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 18/21 | chr5 | 109847077 | ||||||
| chr5:109847218
|
C | T | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2843-439C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 18/21 | chr5 | 109847218 | ||||||
| chr5:109847413
|
T | C | 1 | a0002c0002t0011g0261 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2843-244T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 18/21 | chr5 | 109847413 | ||||||
| chr5:109847442
|
C | T | 1 | a0001c0004t0029g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2843-215C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 18/21 | chr5 | 109847442 | ||||||
| chr5:109847588
|
T | A | 2 | a0001c0003t0003g0164a0001c0003t0003g0165 | 2 | HG00741.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.2843-69T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 18/21 | chr5 | 109847588 | ||||||
| chr5:109847640
|
G | C | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2843-17G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 18/21 | chr5 | 109847640 | ||||||
| chr5:109847640
|
G | T | 81 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2843-17G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 18/21 | chr5 | 109847640 | ||||||
| chr5:109847935
|
A | G | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2976+145A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109847935 | ||||||
| chr5:109847971
|
C | T | 13 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0005g0281others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2976+181C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109847971 | ||||||
| chr5:109848016
|
A | T | 1 | a0001c0001t0001g0188 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2976+226A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109848016 | ||||||
| chr5:109848034
|
C | G | 6 | a0001c0005t0010g0014a0001c0005t0010g0015a0001c0005t0010g0018others(3): Show | 6 | HG02027.hp1 NA18944.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.2976+244C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109848034 | ||||||
| chr5:109848134
|
AGATTAAA others(11): Show |
A | 1 | a0001c0003t0003g0192 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2976+345_2976+362d others(20): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109848134 | ||||||
| chr5:109848283
|
T | C | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2976+493T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109848283 | ||||||
| chr5:109848337
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2976+547T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109848337 | ||||||
| chr5:109848345
|
C | G | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2976+555C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109848345 | ||||||
| chr5:109848372
|
G | T | 1 | a0002c0002t0002g0238 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2976+582G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109848372 | ||||||
| chr5:109848575
|
C | T | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(208): Show | 216 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(213): Show |
intron_variant | MODIFIER | c.2976+785C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109848575 | ||||||
| chr5:109848599
|
A | G | 21 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(18): Show | 22 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.2976+809A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109848599 | ||||||
| chr5:109848699
|
C | G | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2976+909C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109848699 | ||||||
| chr5:109848732
|
C | A | 10 | a0001c0009t0002g0227a0002c0002t0002g0178a0002c0002t0002g0228others(7): Show | 10 | HG00597.hp2 HG01975.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.2976+942C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109848732 | ||||||
| chr5:109848863
|
T | C | 5 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0011t0016g0025others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2976+1073T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109848863 | ||||||
| chr5:109848938
|
C | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2976+1148C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109848938 | ||||||
| chr5:109849027
|
T | G | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2976+1237T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109849027 | ||||||
| chr5:109849269
|
T | C | 1 | a0002c0002t0002g0205 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2976+1479T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109849269 | ||||||
| chr5:109849271
|
G | T | 2 | a0002c0002t0017g0275a0002c0002t0017g0276 | 2 | NA18959.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2976+1481G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109849271 | ||||||
| chr5:109849339
|
C | T | 3 | a0001c0011t0016g0025a0001c0011t0016g0026a0001c0018t0032g0084 | 3 | HG02055.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2976+1549C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109849339 | ||||||
| chr5:109849420
|
C | T | 1 | a0002c0002t0009g0215 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2976+1630C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109849420 | ||||||
| chr5:109849454
|
C | T | 16 | a0001c0005t0003g0054a0001c0005t0003g0169a0001c0005t0008g0009others(13): Show | 16 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2976+1664C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109849454 | ||||||
| chr5:109849599
|
C | T | 2 | a0002c0002t0009g0007a0002c0002t0009g0215 | 2 | HG00642.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2976+1809C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109849599 | ||||||
| chr5:109849619
|
C | T | 1 | a0001c0003t0003g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2976+1829C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109849619 | ||||||
| chr5:109849704
|
T | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2976+1914T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109849704 | ||||||
| chr5:109849713
|
T | G | 82 | a0001c0009t0001g0208a0001c0009t0028g0008a0002c0002t0002g0006others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.2976+1923T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109849713 | ||||||
| chr5:109849714
|
G | GT | 22 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.2976+1932dupT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 109849714 | |||||
| chr5:109849714
|
G | T | 1 | a0001c0001t0005g0058 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2976+1924G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109849714 | ||||||
| chr5:109849751
|
T | C | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2976+1961T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109849751 | ||||||
| chr5:109850075
|
C | T | 11 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0005g0281others(8): Show | 11 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.2976+2285C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109850075 | ||||||
| chr5:109850210
|
A | T | 1 | a0001c0004t0015g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2976+2420A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109850210 | ||||||
| chr5:109850287
|
T | G | 82 | a0001c0004t0036g0024a0001c0009t0001g0208a0002c0002t0002g0006others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.2976+2497T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109850287 | ||||||
| chr5:109850292
|
C | G | 3 | a0003c0007t0001g0194a0003c0007t0001g0195a0003c0007t0001g0196 | 3 | HG00609.hp1 HG00673.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.2976+2502C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109850292 | ||||||
| chr5:109850671
|
A | G | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2976+2881A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109850671 | ||||||
| chr5:109850768
|
G | C | 1 | a0002c0002t0024g0233 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2976+2978G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109850768 | ||||||
| chr5:109850933
|
T | G | 1 | a0001c0001t0001g0055 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2976+3143T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109850933 | ||||||
| chr5:109850953
|
G | A | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2976+3163G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109850953 | ||||||
| chr5:109851176
|
A | G | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2976+3386A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109851176 | ||||||
| chr5:109851237
|
T | C | 1 | a0001c0004t0033g0032 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2976+3447T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109851237 | ||||||
| chr5:109851241
|
G | A | 1 | a0001c0011t0016g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2976+3451G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109851241 | ||||||
| chr5:109851345
|
C | G | 21 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(18): Show | 22 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.2976+3555C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109851345 | ||||||
| chr5:109851425
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2976+3635G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109851425 | ||||||
| chr5:109851534
|
C | T | 1 | a0002c0002t0002g0265 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2977-3606C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109851534 | ||||||
| chr5:109851564
|
C | T | 1 | a0002c0002t0009g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2977-3576C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109851564 | ||||||
| chr5:109851664
|
A | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(103): Show | 110 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.2977-3476A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109851664 | ||||||
| chr5:109851671
|
C | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0055others(61): Show | 67 | HG00639.hp1 HG01071.hp1 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.2977-3469C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109851671 | ||||||
| chr5:109851797
|
G | A | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(184): Show | 192 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(189): Show |
intron_variant | MODIFIER | c.2977-3343G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109851797 | ||||||
| chr5:109852144
|
C | CA | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(103): Show | 110 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.2977-2983dupA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 109852144 | |||||
| chr5:109852144
|
CA | C | 86 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282others(83): Show | 87 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.2977-2983delA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 109852144 | |||||
| chr5:109852156
|
A | T | 1 | a0002c0002t0002g0232 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2977-2984A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109852156 | ||||||
| chr5:109852192
|
G | T | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(208): Show | 216 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(213): Show |
intron_variant | MODIFIER | c.2977-2948G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109852192 | ||||||
| chr5:109852194
|
T | A | 3 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0018t0032g0084 | 3 | HG01891.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2977-2946T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109852194 | ||||||
| chr5:109852214
|
T | C | 7 | a0001c0006t0006g0038a0001c0006t0006g0172a0001c0006t0006g0285others(4): Show | 7 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2977-2926T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109852214 | ||||||
| chr5:109852240
|
A | G | 79 | a0001c0009t0001g0208a0001c0009t0002g0227a0002c0002t0002g0006others(76): Show | 80 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.2977-2900A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109852240 | ||||||
| chr5:109852264
|
C | A | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2977-2876C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109852264 | ||||||
| chr5:109852426
|
C | T | 2 | a0001c0006t0002g0278a0001c0006t0002g0279 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2977-2714C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109852426 | ||||||
| chr5:109852655
|
T | C | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2977-2485T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109852655 | ||||||
| chr5:109853227
|
C | T | 4 | a0001c0003t0003g0160a0001c0003t0003g0161a0001c0003t0003g0162others(1): Show | 4 | HG00597.hp1 HG02056.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.2977-1913C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109853227 | ||||||
| chr5:109853340
|
G | C | 1 | a0002c0002t0002g0272 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2977-1800G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109853340 | ||||||
| chr5:109853343
|
T | C | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2977-1797T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109853343 | ||||||
| chr5:109853391
|
A | G | 1 | a0001c0006t0005g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2977-1749A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109853391 | ||||||
| chr5:109853429
|
C | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(87): Show | 93 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.2977-1711C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109853429 | ||||||
| chr5:109853456
|
A | T | 6 | a0001c0003t0007g0050a0001c0003t0007g0136a0001c0003t0007g0140others(3): Show | 6 | HG01106.hp2 HG01168.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.2977-1684A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109853456 | ||||||
| chr5:109853634
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2977-1506G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109853634 | ||||||
| chr5:109853727
|
G | A | 1 | a0001c0003t0003g0027 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2977-1413G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109853727 | ||||||
| chr5:109853770
|
T | A | 1 | a0001c0006t0022g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2977-1370T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109853770 | ||||||
| chr5:109853856
|
A | G | 6 | a0001c0003t0003g0137a0001c0003t0003g0138a0001c0003t0003g0146others(3): Show | 6 | HG00735.hp2 HG01256.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2977-1284A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109853856 | ||||||
| chr5:109853939
|
T | G | 83 | a0001c0004t0036g0024a0001c0009t0001g0208a0001c0009t0028g0008others(80): Show | 84 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.2977-1201T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109853939 | ||||||
| chr5:109854199
|
C | T | 1 | a0001c0004t0004g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2977-941C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109854199 | ||||||
| chr5:109854434
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2977-706A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109854434 | ||||||
| chr5:109854838
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2977-302T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109854838 | ||||||
| chr5:109854933
|
T | C | 21 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(18): Show | 22 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.2977-207T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109854933 | ||||||
| chr5:109855030
|
G | A | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(208): Show | 217 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(214): Show |
intron_variant | MODIFIER | c.2977-110G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 19/21 | chr5 | 109855030 | ||||||
| chr5:109855454
|
G | A | 1 | a0001c0005t0008g0011 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3171+120G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109855454 | ||||||
| chr5:109855553
|
C | T | 2 | a0001c0004t0004g0051a0001c0004t0004g0053 | 2 | HG02896.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3171+219C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109855553 | ||||||
| chr5:109855915
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3171+581G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109855915 | ||||||
| chr5:109856058
|
G | T | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3171+724G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109856058 | ||||||
| chr5:109856157
|
G | A | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3171+823G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109856157 | ||||||
| chr5:109856211
|
A | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(224): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.3171+877A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109856211 | ||||||
| chr5:109856334
|
C | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(193): Show | 201 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.3171+1000C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109856334 | ||||||
| chr5:109856535
|
T | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(196): Show | 204 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.3171+1201T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109856535 | ||||||
| chr5:109856543
|
G | A | 1 | a0001c0006t0002g0279 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3171+1209G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109856543 | ||||||
| chr5:109856581
|
T | C | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3171+1247T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109856581 | ||||||
| chr5:109856719
|
C | G | 1 | a0001c0006t0006g0285 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3171+1385C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109856719 | ||||||
| chr5:109856737
|
A | G | 1 | a0001c0009t0028g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3171+1403A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109856737 | ||||||
| chr5:109856774
|
C | CGTGT | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3171+1444_3171+144 others(8): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 109856774 | |||||
| chr5:109856782
|
C | T | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(192): Show | 200 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.3171+1448C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109856782 | ||||||
| chr5:109856817
|
A | T | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3171+1483A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109856817 | ||||||
| chr5:109857153
|
G | T | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3171+1819G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109857153 | ||||||
| chr5:109857335
|
A | G | 1 | a0001c0004t0036g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3171+2001A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109857335 | ||||||
| chr5:109857397
|
G | C | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3171+2063G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109857397 | ||||||
| chr5:109857476
|
A | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0005g0111 | 3 | HG01123.hp2 HG01346.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.3171+2142A>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109857476 | ||||||
| chr5:109857500
|
G | A | 81 | a0001c0004t0036g0024a0002c0002t0002g0006a0002c0002t0002g0178others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3171+2166G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109857500 | ||||||
| chr5:109857975
|
T | A | 10 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0006g0038others(7): Show | 10 | HG01891.hp2 HG02451.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.3171+2641T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109857975 | ||||||
| chr5:109858077
|
G | T | 1 | a0010c0020t0003g0174 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3171+2743G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109858077 | ||||||
| chr5:109858358
|
A | G | 1 | a0002c0002t0026g0231 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3171+3024A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109858358 | ||||||
| chr5:109858381
|
G | T | 1 | a0002c0002t0002g0222 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3171+3047G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109858381 | ||||||
| chr5:109858706
|
C | G | 1 | a0002c0002t0025g0263 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3171+3372C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109858706 | ||||||
| chr5:109858735
|
G | A | 1 | a0001c0003t0003g0027 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3171+3401G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109858735 | ||||||
| chr5:109858806
|
T | G | 2 | a0002c0002t0002g0222a0002c0002t0002g0224 | 2 | NA19057.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.3171+3472T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109858806 | ||||||
| chr5:109858929
|
G | C | 21 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(18): Show | 22 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.3171+3595G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109858929 | ||||||
| chr5:109858971
|
CA | C | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3171+3638delA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109858971 | ||||||
| chr5:109859001
|
C | T | 13 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0006g0038others(10): Show | 13 | HG01891.hp2 HG02451.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.3171+3667C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109859001 | ||||||
| chr5:109859145
|
A | G | 1 | a0002c0002t0026g0231 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3171+3811A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109859145 | ||||||
| chr5:109859390
|
T | C | 1 | a0004c0008t0014g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3171+4056T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109859390 | ||||||
| chr5:109859414
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3171+4080G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109859414 | ||||||
| chr5:109859524
|
C | A | 2 | a0001c0004t0004g0030a0001c0004t0004g0031 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3171+4190C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109859524 | ||||||
| chr5:109859525
|
C | T | 1 | a0002c0002t0026g0231 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3171+4191C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109859525 | ||||||
| chr5:109859546
|
T | A | 1 | a0001c0003t0003g0138 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3171+4212T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109859546 | ||||||
| chr5:109859556
|
T | C | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(223): Show | 232 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(229): Show |
intron_variant | MODIFIER | c.3171+4222T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109859556 | ||||||
| chr5:109859584
|
T | C | 8 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0006g0038others(5): Show | 8 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3171+4250T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109859584 | ||||||
| chr5:109859875
|
CT | C | 24 | a0001c0001t0001g0086a0001c0004t0004g0001a0001c0004t0004g0030others(21): Show | 25 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.3171+4557delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 109859875 | |||||
| chr5:109859956
|
A | C | 2 | a0001c0011t0016g0025a0001c0011t0016g0026 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3171+4622A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109859956 | ||||||
| chr5:109860598
|
A | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3172-4438A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109860598 | ||||||
| chr5:109860714
|
G | T | 3 | a0004c0008t0014g0021a0004c0008t0014g0022a0004c0008t0014g0023 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3172-4322G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109860714 | ||||||
| chr5:109860823
|
T | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(86): Show | 92 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.3172-4213T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109860823 | ||||||
| chr5:109860832
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(86): Show | 92 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.3172-4204G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109860832 | ||||||
| chr5:109861201
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3172-3835T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109861201 | ||||||
| chr5:109861208
|
T | TA | 6 | a0001c0006t0006g0038a0001c0006t0006g0172a0001c0006t0006g0285others(3): Show | 6 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.3172-3828_3172-382 others(5): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109861208 | ||||||
| chr5:109861313
|
A | G | 2 | a0001c0003t0003g0164a0001c0003t0003g0165 | 2 | HG00741.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.3172-3723A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109861313 | ||||||
| chr5:109861322
|
G | A | 1 | a0001c0001t0005g0110 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3172-3714G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109861322 | ||||||
| chr5:109861340
|
TG | T | 13 | a0002c0002t0002g0189a0002c0002t0002g0226a0002c0002t0002g0235others(10): Show | 13 | HG00099.hp2 HG01934.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.3172-3695delG | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109861340 | ||||||
| chr5:109861349
|
A | C | 16 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0006g0038others(13): Show | 16 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.3172-3687A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109861349 | ||||||
| chr5:109861479
|
CT | C | 8 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0006t0006g0038others(5): Show | 8 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3172-3554delT | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 109861479 | |||||
| chr5:109861668
|
T | C | 1 | a0002c0002t0024g0233 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3172-3368T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109861668 | ||||||
| chr5:109861783
|
A | C | 4 | a0001c0006t0022g0035a0004c0008t0014g0021a0004c0008t0014g0022others(1): Show | 4 | HG02717.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3172-3253A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109861783 | ||||||
| chr5:109861840
|
A | G | 7 | a0002c0002t0002g0189a0002c0002t0002g0236a0002c0002t0002g0239others(4): Show | 7 | HG00099.hp2 HG01934.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.3172-3196A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109861840 | ||||||
| chr5:109862205
|
C | T | 1 | a0002c0002t0002g0244 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3172-2831C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109862205 | ||||||
| chr5:109862609
|
TAG | T | 3 | a0001c0003t0003g0201a0001c0003t0003g0209a0001c0003t0003g0213 | 3 | HG01167.hp1 HG01943.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.3172-2424_3172-242 others(6): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 109862609 | |||||
| chr5:109862893
|
A | G | 6 | a0001c0006t0006g0038a0001c0006t0006g0172a0001c0006t0006g0285others(3): Show | 6 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.3172-2143A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109862893 | ||||||
| chr5:109863590
|
A | G | 1 | a0002c0002t0002g0220 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3172-1446A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109863590 | ||||||
| chr5:109863639
|
T | C | 1 | a0002c0002t0002g0242 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3172-1397T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109863639 | ||||||
| chr5:109863696
|
G | C | 119 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(116): Show | 121 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.3172-1340G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109863696 | ||||||
| chr5:109863719
|
A | G | 2 | a0002c0002t0002g0258a0002c0002t0002g0259 | 2 | HG01433.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3172-1317A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109863719 | ||||||
| chr5:109864100
|
G | A | 1 | a0002c0002t0009g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3172-936G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109864100 | ||||||
| chr5:109864270
|
T | G | 85 | a0001c0004t0036g0024a0001c0006t0002g0278a0001c0006t0002g0279others(82): Show | 86 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.3172-766T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109864270 | ||||||
| chr5:109864280
|
A | G | 85 | a0001c0004t0036g0024a0001c0006t0002g0278a0001c0006t0002g0279others(82): Show | 86 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.3172-756A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109864280 | ||||||
| chr5:109864333
|
A | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(88): Show | 94 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.3172-703A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109864333 | ||||||
| chr5:109864360
|
A | G | 1 | a0001c0003t0003g0167 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3172-676A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109864360 | ||||||
| chr5:109864362
|
A | G | 3 | a0002c0002t0002g0219a0002c0002t0002g0221a0002c0002t0002g0225 | 3 | NA18942.hp1 NA18945.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.3172-674A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109864362 | ||||||
| chr5:109864389
|
T | G | 21 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(18): Show | 22 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.3172-647T>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109864389 | ||||||
| chr5:109864448
|
T | A | 1 | a0001c0005t0008g0012 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3172-588T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109864448 | ||||||
| chr5:109864548
|
C | A | 6 | a0001c0006t0006g0038a0001c0006t0006g0172a0001c0006t0006g0285others(3): Show | 6 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.3172-488C>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109864548 | ||||||
| chr5:109864852
|
A | C | 83 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0009t0002g0227others(80): Show | 84 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.3172-184A>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109864852 | ||||||
| chr5:109864925
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3172-111T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109864925 | ||||||
| chr5:109864989
|
T | C | 1 | a0002c0002t0002g0237 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3172-47T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109864989 | ||||||
| chr5:109865009
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3172-27G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 20/21 | chr5 | 109865009 | ||||||
| chr5:109865376
|
C | G | 1 | a0001c0001t0005g0058 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3282+230C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109865376 | ||||||
| chr5:109865416
|
A | G | 1 | a0002c0002t0002g0260 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3282+270A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109865416 | ||||||
| chr5:109865429
|
C | T | 21 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(18): Show | 22 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.3282+283C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109865429 | ||||||
| chr5:109865455
|
C | G | 3 | a0001c0004t0013g0049a0001c0004t0013g0214a0001c0004t0013g0282 | 3 | HG01192.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3282+309C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109865455 | ||||||
| chr5:109865591
|
G | A | 1 | a0001c0005t0008g0011 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3282+445G>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109865591 | ||||||
| chr5:109865650
|
G | T | 1 | a0001c0006t0006g0172 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3282+504G>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109865650 | ||||||
| chr5:109865774
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0091a0001c0001t0001g0108 | 4 | HG03490.hp2 HG03492.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.3282+628T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109865774 | ||||||
| chr5:109865945
|
C | G | 3 | a0002c0002t0002g0219a0002c0002t0002g0221a0002c0002t0002g0225 | 3 | NA18942.hp1 NA18945.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.3282+799C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109865945 | ||||||
| chr5:109865977
|
G | C | 1 | a0001c0003t0003g0129 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3282+831G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109865977 | ||||||
| chr5:109866042
|
A | G | 1 | a0001c0018t0032g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3283-804A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109866042 | ||||||
| chr5:109866122
|
C | T | 109 | a0001c0004t0004g0001a0001c0004t0004g0030a0001c0004t0004g0031others(106): Show | 111 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.3283-724C>T | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109866122 | ||||||
| chr5:109866183
|
T | C | 4 | a0001c0005t0008g0009a0001c0005t0008g0010a0001c0005t0008g0016others(1): Show | 4 | HG00140.hp1 HG00639.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.3283-663T>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109866183 | ||||||
| chr5:109866234
|
G | C | 1 | a0001c0004t0013g0049 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3283-612G>C | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109866234 | ||||||
| chr5:109866257
|
T | TA | 85 | a0001c0004t0036g0024a0001c0006t0002g0278a0001c0006t0002g0279others(82): Show | 86 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.3283-588dupA | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr5 | 109866257 | |||||
| chr5:109866331
|
C | G | 83 | a0001c0006t0002g0278a0001c0006t0002g0279a0001c0009t0002g0227others(80): Show | 84 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.3283-515C>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109866331 | ||||||
| chr5:109866350
|
T | A | 1 | a0001c0005t0003g0054 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3283-496T>A | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109866350 | ||||||
| chr5:109866449
|
A | G | 2 | a0004c0008t0014g0022a0004c0008t0014g0023 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3283-397A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109866449 | ||||||
| chr5:109866693
|
A | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(101): Show | 108 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.3283-153A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109866693 | ||||||
| chr5:109866729
|
A | G | 4 | a0002c0002t0002g0219a0002c0002t0002g0221a0002c0002t0002g0225others(1): Show | 4 | NA18942.hp1 NA18945.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.3283-117A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109866729 | ||||||
| chr5:109866767
|
A | G | 3 | a0001c0011t0016g0025a0001c0011t0016g0026a0001c0018t0032g0084 | 3 | HG02055.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3283-79A>G | MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 21/21 | chr5 | 109866767 |