geneid | 10020 |
---|---|
ensemblid | ENSG00000159921.20 |
hgncid | 23657 |
symbol | GNE |
name | glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase |
refseq_nuc | NM_001128227.3 |
refseq_prot | NP_001121699.1 |
ensembl_nuc | ENST00000396594.8 |
ensembl_prot | ENSP00000379839.3 |
mane_status | MANE Plus Clinical |
chr | chr9 |
start | 36214441 |
end | 36276978 |
strand | - |
ver | v1.2 |
region | chr9:36214441-36276978 |
region5000 | chr9:36209441-36281978 |
regionname0 | GNE_chr9_36214441_36276978 |
regionname5000 | GNE_chr9_36209441_36281978 |
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 | 753 | 354 | 84 | 72 | 138 | 16 | 42 | 102 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0002 | 0/0 | 753 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
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 | 1/1 | 2262 | 346 | 78 | 72 | 138 | 16 | 40 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
c0002 | 0/0 | 2262 | 8 | 6 | 0 | 0 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
c0003 | 0/0 | 2262 | 2 | 0 | 0 | 2 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
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 | 1/0 | 2959 | 80 | 11 | 9 | 46 | 4 | 9 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0002 | 0/0 | 2991 | 33 | 5 | 5 | 21 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0003 | 0/0 | 2985 | 16 | 1 | 1 | 13 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0004 | 0/0 | 2960 | 15 | 0 | 4 | 11 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0005 | 0/0 | 2974 | 13 | 1 | 3 | 6 | 1 | 2 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0006 | 0/0 | 2976 | 12 | 1 | 5 | 5 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0007 | 0/0 | 2977 | 11 | 0 | 5 | 4 | 1 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0008 | 0/0 | 2975 | 10 | 3 | 2 | 4 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0009 | 0/0 | 2987 | 9 | 0 | 0 | 7 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0010 | 0/1 | 2962 | 9 | 0 | 3 | 4 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0011 | 0/0 | 2978 | 7 | 1 | 4 | 1 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0012 | 0/0 | 2971 | 5 | 5 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0013 | 0/0 | 2986 | 5 | 4 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0014 | 0/0 | 2970 | 5 | 4 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0015 | 0/0 | 2985 | 3 | 0 | 2 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0016 | 0/0 | 2981 | 3 | 0 | 0 | 1 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0017 | 0/0 | 2996 | 3 | 0 | 0 | 0 | 0 | 3 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0018 | 0/0 | 2994 | 3 | 1 | 0 | 1 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0019 | 0/0 | 2983 | 3 | 0 | 3 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0020 | 0/0 | 2981 | 3 | 0 | 0 | 1 | 2 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0021 | 0/0 | 2961 | 3 | 0 | 3 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0022 | 0/0 | 2974 | 3 | 0 | 1 | 0 | 1 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0023 | 0/0 | 2989 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0024 | 0/0 | 2979 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0025 | 0/0 | 2972 | 2 | 0 | 2 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0026 | 0/0 | 2970 | 2 | 1 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0027 | 0/0 | 2973 | 2 | 0 | 0 | 1 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0028 | 0/0 | 2961 | 2 | 0 | 2 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0029 | 0/0 | 2990 | 2 | 1 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0030 | 0/0 | 2984 | 2 | 0 | 0 | 0 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0031 | 0/0 | 2993 | 2 | 0 | 1 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0032 | 0/0 | 2991 | 2 | 0 | 0 | 0 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0033 | 0/0 | 2989 | 2 | 0 | 0 | 2 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0034 | 0/0 | 2985 | 2 | 1 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0035 | 0/0 | 2983 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0036 | 0/0 | 2995 | 2 | 0 | 0 | 2 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0037 | 0/0 | 2965 | 2 | 0 | 2 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0038 | 0/0 | 2988 | 2 | 1 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0039 | 0/0 | 2988 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0040 | 0/0 | 2987 | 2 | 1 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0041 | 0/0 | 2985 | 2 | 0 | 0 | 1 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0042 | 0/0 | 2956 | 2 | 0 | 1 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0043 | 0/0 | 2974 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0044 | 0/0 | 2950 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0045 | 0/0 | 2988 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0046 | 0/0 | 2985 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0047 | 0/0 | 2965 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0048 | 0/0 | 2993 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0049 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0050 | 0/0 | 2978 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0051 | 0/0 | 2994 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0052 | 0/0 | 2978 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0053 | 0/0 | 2991 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0054 | 0/0 | 2984 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0055 | 0/0 | 2978 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0056 | 0/0 | 2986 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0057 | 0/0 | 2979 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0058 | 0/0 | 2977 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0059 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0060 | 0/0 | 2975 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0061 | 0/0 | 2980 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0062 | 0/0 | 2976 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0063 | 0/0 | 2974 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0064 | 0/0 | 2974 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0065 | 0/0 | 2997 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0066 | 0/0 | 2971 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0067 | 0/0 | 2981 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0068 | 0/0 | 2969 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0069 | 0/0 | 2967 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0070 | 0/0 | 2991 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0071 | 0/0 | 2997 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0072 | 0/0 | 2971 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0073 | 0/0 | 2992 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0074 | 0/0 | 2986 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0075 | 0/0 | 2995 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0076 | 0/0 | 2989 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0077 | 0/0 | 2987 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0078 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0079 | 0/0 | 2981 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0080 | 0/0 | 2993 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0081 | 0/0 | 2991 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0082 | 0/0 | 2984 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0083 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0084 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0085 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0086 | 0/0 | 2979 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0087 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0088 | 0/0 | 2959 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0089 | 0/0 | 2959 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0090 | 0/0 | 2993 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0091 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0092 | 0/0 | 2982 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0093 | 0/0 | 2980 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0094 | 0/0 | 2972 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0095 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0096 | 0/0 | 2994 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0097 | 0/0 | 2987 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0098 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0099 | 0/0 | 2981 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
t0100 | 0/0 | 2973 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
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 | 0 | 0 | 0 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0240 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0285 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
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 | 1/1 | 2262 | 346 | 78 | 72 | 138 | 16 | 40 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0002 | 0/0 | 2262 | 8 | 6 | 0 | 0 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0002c0003 | 0/0 | 2262 | 2 | 0 | 0 | 2 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5220 | 80 | 11 | 9 | 46 | 4 | 9 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0002 | 0/0 | 5252 | 33 | 5 | 5 | 21 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0003 | 0/0 | 5246 | 16 | 1 | 1 | 13 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0004 | 0/0 | 5221 | 15 | 0 | 4 | 11 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0005 | 0/0 | 5235 | 13 | 1 | 3 | 6 | 1 | 2 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0006 | 0/0 | 5237 | 12 | 1 | 5 | 5 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0007 | 0/0 | 5238 | 11 | 0 | 5 | 4 | 1 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0008 | 0/0 | 5236 | 10 | 3 | 2 | 4 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0009 | 0/0 | 5248 | 8 | 0 | 0 | 6 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0010 | 0/1 | 5223 | 9 | 0 | 3 | 4 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0011 | 0/0 | 5239 | 7 | 1 | 4 | 1 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0012 | 0/0 | 5232 | 5 | 5 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0013 | 0/0 | 5247 | 5 | 4 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0014 | 0/0 | 5231 | 5 | 4 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0015 | 0/0 | 5246 | 3 | 0 | 2 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0016 | 0/0 | 5242 | 3 | 0 | 0 | 1 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0017 | 0/0 | 5257 | 3 | 0 | 0 | 0 | 0 | 3 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0018 | 0/0 | 5255 | 2 | 1 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0019 | 0/0 | 5244 | 3 | 0 | 3 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0020 | 0/0 | 5242 | 3 | 0 | 0 | 1 | 2 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0021 | 0/0 | 5222 | 3 | 0 | 3 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0022 | 0/0 | 5235 | 3 | 0 | 1 | 0 | 1 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0023 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0025 | 0/0 | 5233 | 2 | 0 | 2 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0026 | 0/0 | 5231 | 2 | 1 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0027 | 0/0 | 5234 | 2 | 0 | 0 | 1 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0028 | 0/0 | 5222 | 2 | 0 | 2 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0029 | 0/0 | 5251 | 2 | 1 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0030 | 0/0 | 5245 | 2 | 0 | 0 | 0 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0031 | 0/0 | 5254 | 2 | 0 | 1 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0032 | 0/0 | 5252 | 2 | 0 | 0 | 0 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0033 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0034 | 0/0 | 5246 | 2 | 1 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0035 | 0/0 | 5244 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0036 | 0/0 | 5256 | 2 | 0 | 0 | 2 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0037 | 0/0 | 5226 | 2 | 0 | 2 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0038 | 0/0 | 5249 | 2 | 1 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0039 | 0/0 | 5249 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0040 | 0/0 | 5248 | 2 | 1 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0041 | 0/0 | 5246 | 2 | 0 | 0 | 1 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0042 | 0/0 | 5217 | 2 | 0 | 1 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0043 | 0/0 | 5235 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0044 | 0/0 | 5211 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0045 | 0/0 | 5249 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0046 | 0/0 | 5246 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0047 | 0/0 | 5226 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0048 | 0/0 | 5254 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0050 | 0/0 | 5239 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0052 | 0/0 | 5239 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0053 | 0/0 | 5252 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0054 | 0/0 | 5245 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0055 | 0/0 | 5239 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0056 | 0/0 | 5247 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0057 | 0/0 | 5240 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0058 | 0/0 | 5238 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0059 | 0/0 | 5238 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0060 | 0/0 | 5236 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0061 | 0/0 | 5241 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0062 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0063 | 0/0 | 5235 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0064 | 0/0 | 5235 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0065 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0066 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0067 | 0/0 | 5242 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0068 | 0/0 | 5230 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0069 | 0/0 | 5228 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0070 | 0/0 | 5252 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0072 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0073 | 0/0 | 5253 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0074 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0075 | 0/0 | 5256 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0076 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0077 | 0/0 | 5248 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0078 | 0/0 | 5246 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0079 | 0/0 | 5242 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0080 | 0/0 | 5254 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0081 | 0/0 | 5252 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0082 | 0/0 | 5245 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0083 | 0/0 | 5249 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0084 | 0/0 | 5238 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0085 | 0/0 | 5244 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0086 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0087 | 0/0 | 5222 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0088 | 0/0 | 5220 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0089 | 0/0 | 5220 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0090 | 0/0 | 5254 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0091 | 0/0 | 5249 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0092 | 0/0 | 5243 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0093 | 0/0 | 5241 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0094 | 0/0 | 5233 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0095 | 0/0 | 5249 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0096 | 0/0 | 5255 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0097 | 0/0 | 5248 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0098 | 0/0 | 5244 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0099 | 0/0 | 5242 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0001t0100 | 0/0 | 5234 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0002t0018 | 0/0 | 5255 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0002t0023 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0002t0024 | 0/0 | 5240 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0002t0035 | 0/0 | 5244 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0002t0049 | 0/0 | 5246 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0002t0051 | 0/0 | 5255 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0001c0002t0071 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0002c0003t0009 | 0/0 | 5248 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
a0002c0003t0033 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | copy fasta | chr9 | 36209441 | 36281978 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0240 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0004g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0006g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0006g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0006g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0006g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0007g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0007g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0007g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0007g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0007g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0007g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0007g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0007g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0008g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0008g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0008g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0008g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0008g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0008g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0008g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0008g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0009g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0009g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0009g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0009g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0009g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0009g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0009g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0009g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0010g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0010g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0010g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0010g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0010g0285 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0010g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0010g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0010g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0010g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0011g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0011g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0011g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0011g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0011g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0011g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0011g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0012g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0012g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0012g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0012g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0012g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0013g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0013g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0013g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0013g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0013g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0014g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0014g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0014g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0014g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0014g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0015g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0015g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0015g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0016g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0016g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0016g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0017g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0017g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0017g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0018g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0018g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0019g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0019g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0019g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0020g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0020g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0020g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0021g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0021g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0021g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0022g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0022g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0022g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0023g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0025g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0025g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0026g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0026g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0027g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0027g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0028g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0028g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0029g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0029g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0030g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0030g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0031g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0031g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0032g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0033g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0034g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0034g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0035g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0036g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0036g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0037g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0037g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0038g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0038g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0039g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0039g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0040g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0040g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0041g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0041g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0042g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0042g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0043g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0043g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0044g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0044g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0045g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0045g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0046g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0046g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0047g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0048g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0050g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0052g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0053g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0054g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0055g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0056g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0057g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0058g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0059g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0060g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0061g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0062g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0063g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0064g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0065g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0066g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0067g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0068g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0069g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0070g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0072g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0073g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0074g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0075g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0076g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0077g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0078g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0079g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0080g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0081g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0082g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0083g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0084g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0085g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0086g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0087g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0088g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0089g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0090g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0091g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0092g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0093g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0094g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0095g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0096g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0097g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0098g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0099g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0001t0100g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0002t0018g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0002t0023g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0002t0024g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0002t0024g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0002t0035g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0002t0049g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0002t0051g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0001c0002t0071g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0002c0003t0009g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
a0002c0003t0033g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0010 | g0288 | EUR | GBR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00099 | hp2 | a0001 | c0001 | t0022 | g0164 | EUR | GBR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0296 | EUR | GBR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0198 | EUR | GBR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00280 | hp1 | a0001 | c0001 | t0007 | g0178 | EUR | FIN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00280 | hp2 | a0001 | c0001 | t0031 | g0226 | EUR | FIN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00408 | hp2 | a0001 | c0001 | t0009 | g0045 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0222 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00544 | hp1 | a0001 | c0001 | t0078 | g0048 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00609 | hp1 | a0001 | c0001 | t0010 | g0274 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00639 | hp1 | a0001 | c0001 | t0010 | g0286 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0277 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00738 | hp1 | a0001 | c0001 | t0015 | g0172 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00738 | hp2 | a0001 | c0001 | t0010 | g0289 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00741 | hp1 | a0001 | c0001 | t0015 | g0150 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG00741 | hp2 | a0001 | c0001 | t0011 | g0211 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01069 | hp1 | a0001 | c0001 | t0011 | g0209 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01071 | hp1 | a0001 | c0001 | t0011 | g0208 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01071 | hp2 | a0001 | c0001 | t0026 | g0213 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01074 | hp1 | a0001 | c0001 | t0031 | g0128 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01074 | hp2 | a0001 | c0001 | t0014 | g0083 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01081 | hp1 | a0001 | c0001 | t0006 | g0224 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01081 | hp2 | a0001 | c0001 | t0010 | g0273 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01099 | hp1 | a0001 | c0001 | t0022 | g0148 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01106 | hp2 | a0001 | c0001 | t0025 | g0217 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01109 | hp1 | a0001 | c0001 | t0096 | g0011 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01109 | hp2 | a0001 | c0001 | t0042 | g0260 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01167 | hp2 | a0001 | c0001 | t0008 | g0169 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0193 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01169 | hp1 | a0001 | c0001 | t0006 | g0194 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01175 | hp1 | a0001 | c0001 | t0008 | g0175 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01175 | hp2 | a0001 | c0001 | t0053 | g0031 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01192 | hp1 | a0001 | c0001 | t0006 | g0197 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01243 | hp1 | a0001 | c0001 | t0006 | g0225 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01243 | hp2 | a0001 | c0001 | t0013 | g0075 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01255 | hp1 | a0001 | c0001 | t0040 | g0350 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01255 | hp2 | a0001 | c0001 | t0065 | g0151 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01256 | hp1 | a0001 | c0001 | t0028 | g0145 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01256 | hp2 | a0001 | c0001 | t0037 | g0305 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01257 | hp1 | a0001 | c0001 | t0007 | g0174 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01257 | hp2 | a0001 | c0001 | t0034 | g0092 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01258 | hp1 | a0001 | c0001 | t0007 | g0176 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01258 | hp2 | a0001 | c0001 | t0037 | g0290 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0302 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01261 | hp2 | a0001 | c0001 | t0011 | g0182 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01346 | hp2 | a0001 | c0001 | t0028 | g0179 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01361 | hp1 | a0001 | c0001 | t0063 | g0200 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01496 | hp1 | a0001 | c0001 | t0007 | g0168 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01515 | hp1 | a0001 | c0001 | t0062 | g0210 | EUR | IBS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01515 | hp2 | a0001 | c0001 | t0020 | g0061 | EUR | IBS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01516 | hp1 | a0001 | c0001 | t0008 | g0177 | EUR | IBS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0325 | EUR | IBS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01517 | hp1 | a0001 | c0001 | t0020 | g0062 | EUR | IBS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0324 | EUR | IBS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01884 | hp1 | a0001 | c0001 | t0100 | g0272 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01884 | hp2 | a0001 | c0002 | t0049 | g0027 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01891 | hp2 | a0001 | c0002 | t0051 | g0341 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01928 | hp1 | a0001 | c0001 | t0058 | g0205 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0262 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01934 | hp2 | a0001 | c0001 | t0064 | g0221 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01943 | hp1 | a0001 | c0001 | t0007 | g0161 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01943 | hp2 | a0001 | c0001 | t0005 | g0199 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01952 | hp1 | a0001 | c0001 | t0021 | g0316 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01952 | hp2 | a0001 | c0001 | t0025 | g0195 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01975 | hp1 | a0001 | c0001 | t0007 | g0140 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01978 | hp1 | a0001 | c0001 | t0019 | g0051 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01978 | hp2 | a0001 | c0001 | t0061 | g0219 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01981 | hp1 | a0001 | c0001 | t0005 | g0214 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01981 | hp2 | a0001 | c0001 | t0038 | g0130 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01993 | hp1 | a0001 | c0001 | t0021 | g0264 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01993 | hp2 | a0001 | c0001 | t0019 | g0064 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02040 | hp1 | a0001 | c0001 | t0009 | g0044 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02040 | hp2 | a0001 | c0001 | t0005 | g0202 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02055 | hp1 | a0001 | c0001 | t0013 | g0072 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02056 | hp1 | a0001 | c0001 | t0082 | g0021 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0265 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02071 | hp2 | a0001 | c0001 | t0008 | g0153 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02074 | hp1 | a0001 | c0001 | t0086 | g0020 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02080 | hp1 | a0001 | c0001 | t0006 | g0184 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02080 | hp2 | a0001 | c0001 | t0009 | g0055 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02129 | hp1 | a0001 | c0001 | t0005 | g0207 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02135 | hp2 | a0001 | c0001 | t0007 | g0142 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02148 | hp1 | a0001 | c0001 | t0019 | g0065 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02148 | hp2 | a0001 | c0001 | t0021 | g0319 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CDX | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | CDX | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02257 | hp1 | a0001 | c0001 | t0038 | g0351 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02258 | hp1 | a0001 | c0001 | t0026 | g0223 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02258 | hp2 | a0001 | c0001 | t0011 | g0352 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02280 | hp1 | a0001 | c0001 | t0044 | g0342 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02293 | hp1 | a0001 | c0001 | t0005 | g0204 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02293 | hp2 | a0001 | c0001 | t0004 | g0279 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02451 | hp2 | a0001 | c0001 | t0047 | g0005 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02572 | hp1 | a0001 | c0001 | t0091 | g0355 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02572 | hp2 | a0001 | c0001 | t0039 | g0139 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02615 | hp1 | a0001 | c0001 | t0087 | g0232 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02615 | hp2 | a0001 | c0001 | t0080 | g0124 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02622 | hp1 | a0001 | c0001 | t0045 | g0018 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02630 | hp2 | a0001 | c0001 | t0008 | g0152 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02647 | hp1 | a0001 | c0001 | t0093 | g0353 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02647 | hp2 | a0001 | c0002 | t0035 | g0063 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02683 | hp1 | a0001 | c0001 | t0017 | g0078 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02683 | hp2 | a0001 | c0001 | t0042 | g0256 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0216 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02717 | hp2 | a0001 | c0001 | t0083 | g0119 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02723 | hp1 | a0001 | c0001 | t0008 | g0143 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02723 | hp2 | a0001 | c0001 | t0043 | g0090 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02735 | hp1 | a0001 | c0001 | t0075 | g0033 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02738 | hp1 | a0001 | c0001 | t0007 | g0154 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02738 | hp2 | a0001 | c0001 | t0077 | g0125 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02809 | hp2 | a0001 | c0001 | t0048 | g0073 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02818 | hp1 | a0001 | c0001 | t0098 | g0016 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02818 | hp2 | a0001 | c0002 | t0023 | g0026 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02896 | hp1 | a0001 | c0001 | t0012 | g0007 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02896 | hp2 | a0001 | c0001 | t0092 | g0354 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02897 | hp1 | a0001 | c0001 | t0012 | g0006 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02897 | hp2 | a0001 | c0001 | t0099 | g0012 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02922 | hp1 | a0001 | c0001 | t0012 | g0002 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02922 | hp2 | a0001 | c0001 | t0014 | g0087 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02965 | hp1 | a0001 | c0002 | t0024 | g0025 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02965 | hp2 | a0001 | c0001 | t0043 | g0234 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02976 | hp2 | a0001 | c0001 | t0066 | g0180 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03098 | hp1 | a0001 | c0001 | t0045 | g0010 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03098 | hp2 | a0001 | c0001 | t0039 | g0138 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03130 | hp1 | a0001 | c0001 | t0094 | g0235 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03130 | hp2 | a0001 | c0001 | t0014 | g0084 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03195 | hp1 | a0001 | c0001 | t0056 | g0344 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03195 | hp2 | a0001 | c0001 | t0014 | g0233 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03225 | hp1 | a0001 | c0001 | t0084 | g0089 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03225 | hp2 | a0001 | c0001 | t0012 | g0004 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03239 | hp1 | a0001 | c0001 | t0068 | g0173 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03239 | hp2 | a0001 | c0001 | t0011 | g0196 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03453 | hp1 | a0001 | c0001 | t0035 | g0067 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03453 | hp2 | a0001 | c0001 | t0040 | g0348 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03486 | hp1 | a0001 | c0001 | t0095 | g0017 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03486 | hp2 | a0001 | c0001 | t0034 | g0088 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03490 | hp1 | a0001 | c0001 | t0032 | g0001 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03490 | hp2 | a0001 | c0001 | t0069 | g0156 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03491 | hp2 | a0001 | c0001 | t0015 | g0167 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03492 | hp2 | a0001 | c0001 | t0032 | g0001 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03516 | hp1 | a0001 | c0001 | t0014 | g0237 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03516 | hp2 | a0001 | c0002 | t0024 | g0028 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03579 | hp1 | a0001 | c0001 | t0085 | g0349 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03579 | hp2 | a0001 | c0001 | t0013 | g0068 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0104 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03669 | hp2 | a0001 | c0001 | t0079 | g0123 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03688 | hp1 | a0001 | c0001 | t0030 | g0312 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03688 | hp2 | a0001 | c0001 | t0009 | g0039 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03704 | hp1 | a0001 | c0001 | t0009 | g0032 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03704 | hp2 | a0001 | c0001 | t0076 | g0103 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03710 | hp1 | a0001 | c0002 | t0018 | g0023 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0269 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03834 | hp2 | a0001 | c0001 | t0070 | g0047 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03927 | hp1 | a0001 | c0001 | t0016 | g0155 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03927 | hp2 | a0001 | c0001 | t0006 | g0215 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03942 | hp1 | a0001 | c0002 | t0071 | g0024 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03942 | hp2 | a0001 | c0001 | t0022 | g0141 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG04115 | hp2 | a0001 | c0001 | t0041 | g0100 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG04184 | hp1 | a0001 | c0001 | t0017 | g0049 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG04199 | hp1 | a0001 | c0001 | t0030 | g0313 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0098 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG04204 | hp1 | a0001 | c0001 | t0016 | g0165 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG04204 | hp2 | a0001 | c0001 | t0017 | g0038 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG04228 | hp1 | a0001 | c0001 | t0027 | g0203 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18522 | hp1 | a0001 | c0001 | t0054 | g0071 | AFR | YRI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | YRI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18612 | hp1 | a0001 | c0001 | t0011 | g0192 | EAS | CHB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18747 | hp1 | a0001 | c0001 | t0027 | g0147 | EAS | CHB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18747 | hp2 | a0001 | c0001 | t0089 | g0283 | EAS | CHB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0066 | AFR | YRI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18906 | hp2 | a0001 | c0001 | t0046 | g0015 | AFR | YRI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18943 | hp1 | a0001 | c0001 | t0009 | g0050 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18944 | hp1 | a0001 | c0001 | t0007 | g0170 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18945 | hp1 | a0001 | c0001 | t0009 | g0037 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18946 | hp1 | a0001 | c0001 | t0006 | g0185 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18951 | hp2 | a0002 | c0003 | t0033 | g0186 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18952 | hp1 | a0001 | c0001 | t0020 | g0043 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18953 | hp2 | a0001 | c0001 | t0005 | g0189 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18954 | hp1 | a0001 | c0001 | t0088 | g0321 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18954 | hp2 | a0001 | c0001 | t0010 | g0282 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18956 | hp1 | a0001 | c0001 | t0074 | g0030 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18959 | hp1 | a0001 | c0001 | t0018 | g0113 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18959 | hp2 | a0001 | c0001 | t0008 | g0157 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18960 | hp2 | a0001 | c0001 | t0006 | g0183 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18967 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0340 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18971 | hp2 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18979 | hp1 | a0001 | c0001 | t0004 | g0314 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18984 | hp1 | a0001 | c0001 | t0036 | g0127 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18986 | hp2 | a0001 | c0001 | t0081 | g0112 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18990 | hp2 | a0001 | c0001 | t0008 | g0110 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18992 | hp2 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18993 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18993 | hp2 | a0001 | c0001 | t0033 | g0040 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18995 | hp1 | a0001 | c0001 | t0006 | g0190 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19007 | hp2 | a0001 | c0001 | t0005 | g0206 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19011 | hp1 | a0001 | c0001 | t0008 | g0146 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | LWK | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19030 | hp2 | a0001 | c0001 | t0059 | g0343 | AFR | LWK | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19043 | hp1 | a0001 | c0001 | t0044 | g0346 | AFR | LWK | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | LWK | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19062 | hp1 | a0001 | c0001 | t0010 | g0271 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19062 | hp2 | a0001 | c0001 | t0005 | g0220 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19063 | hp2 | a0002 | c0003 | t0009 | g0188 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19066 | hp1 | a0001 | c0001 | t0006 | g0187 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19066 | hp2 | a0001 | c0001 | t0010 | g0315 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19079 | hp1 | a0001 | c0001 | t0090 | g0149 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19081 | hp1 | a0001 | c0001 | t0007 | g0171 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19084 | hp1 | a0001 | c0001 | t0009 | g0058 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19084 | hp2 | a0001 | c0001 | t0016 | g0162 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19086 | hp1 | a0001 | c0001 | t0041 | g0105 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19089 | hp1 | a0001 | c0001 | t0072 | g0106 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19091 | hp1 | a0001 | c0001 | t0036 | g0126 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19240 | hp1 | a0001 | c0001 | t0046 | g0014 | AFR | YRI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA19240 | hp2 | a0001 | c0001 | t0012 | g0003 | AFR | YRI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ASW | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA20129 | hp2 | a0001 | c0001 | t0013 | g0070 | AFR | ASW | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0336 | EUR | TSI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA20752 | hp2 | a0001 | c0001 | t0060 | g0191 | EUR | TSI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA20805 | hp1 | a0001 | c0001 | t0057 | g0212 | EUR | TSI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA20805 | hp2 | a0001 | c0001 | t0029 | g0118 | EUR | TSI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG01123 | hp2 | a0001 | c0001 | t0067 | g0144 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02109 | hp1 | a0001 | c0001 | t0073 | g0297 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02486 | hp1 | a0001 | c0001 | t0013 | g0069 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02486 | hp2 | a0001 | c0001 | t0052 | g0347 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02559 | hp1 | a0001 | c0001 | t0050 | g0074 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG02559 | hp2 | a0001 | c0001 | t0029 | g0091 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG03471 | hp2 | a0001 | c0001 | t0097 | g0013 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG06807 | hp1 | a0001 | c0001 | t0055 | g0345 | AFR | USA | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
HG06807 | hp2 | a0001 | c0001 | t0023 | g0236 | AFR | USA | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA18955 | hp2 | a0001 | c0001 | t0007 | g0181 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | USA | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA20300 | hp2 | a0001 | c0001 | t0008 | g0201 | AFR | USA | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA21309 | hp1 | a0001 | c0001 | t0018 | g0099 | AFR | LWK | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0010 | g0285 | REF | REF | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0240 | REF | REF | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:36246120
|
T | A | 1 | a0002 | 2 | NA18951.hp2 NA19063.hp2 |
missense_variant | MODERATE | c.620A>T | p.Asp207Val | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/12 | 654/5220 | 620/2262 | 207/753 | chr9 | 36246120 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:36246047
|
G | A | 1 | a0001c0002 | 8 | HG01884.hp2 HG01891.hp2 HG02647.hp2 others(5): Show |
synonymous_variant | LOW | c.693C>T | p.Ile231Ile | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/12 | 727/5220 | 693/2262 | 231/753 | chr9 | 36246047 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:36214576
|
C | T | 1 | a0001c0001t0036 | 2 | NA18984.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2789G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2789 | chr9 | 36214576 | |||||
chr9:36214638
|
G | T | 1 | a0001c0001t0078 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2727C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2727 | chr9 | 36214638 | |||||
chr9:36214653
|
G | A | 1 | a0001c0001t0062 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2712C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2712 | chr9 | 36214653 | |||||
chr9:36214654
|
C | T | 1 | a0001c0001t0062 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2711G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2711 | chr9 | 36214654 | |||||
chr9:36214815
|
C | T | 1 | a0001c0001t0081 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2550G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2550 | chr9 | 36214815 | |||||
chr9:36214974
|
G | A | 73 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(70): Show | 190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*2391C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2391 | chr9 | 36214974 | |||||
chr9:36215099
|
C | T | 1 | a0001c0001t0088 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2266G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2266 | chr9 | 36215099 | |||||
chr9:36215154
|
G | C | 1 | a0001c0001t0063 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2211C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2211 | chr9 | 36215154 | |||||
chr9:36215168
|
C | CA | 1 | a0001c0001t0004 | 15 | HG00609.hp2 HG00735.hp2 HG01261.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2196dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2196 | chr9 | 36215168 | |||||
chr9:36215209
|
C | G | 2 | a0001c0001t0013a0001c0001t0054 | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2156G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2156 | chr9 | 36215209 | |||||
chr9:36215309
|
G | A | 2 | a0001c0001t0021a0001c0001t0089 | 4 | HG01952.hp1 HG01993.hp1 HG02148.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2056C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2056 | chr9 | 36215309 | |||||
chr9:36215539
|
C | G | 12 | a0001c0001t0002a0001c0001t0017a0001c0001t0018others(9): Show | 49 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1826G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1826 | chr9 | 36215539 | |||||
chr9:36215584
|
C | T | 15 | a0001c0001t0007a0001c0001t0008a0001c0001t0012others(12): Show | 46 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1781G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1781 | chr9 | 36215584 | |||||
chr9:36216297
|
T | A | 3 | a0001c0001t0055a0001c0001t0056a0001c0001t0059 | 3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1068A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1068 | chr9 | 36216297 | |||||
chr9:36216311
|
G | T | 2 | a0001c0001t0013a0001c0001t0054 | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1054C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1054 | chr9 | 36216311 | |||||
chr9:36216327
|
A | ATG | 2 | a0001c0001t0021a0001c0001t0087 | 4 | HG01952.hp1 HG01993.hp1 HG02148.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1036_*1037dupCA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216327
|
A | ATGTGTGT others(1): Show |
2 | a0001c0001t0028a0001c0001t0100 | 3 | HG01256.hp1 HG01346.hp2 HG01884.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1030_*1037dupCACA others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216327
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0047 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1026_*1037dupCACA others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216327
|
A | ATGTGTGT others(7): Show |
2 | a0001c0001t0026a0001c0002t0024 | 4 | HG01071.hp2 HG02258.hp1 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1024_*1037dupCACA others(10): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216327
|
A | ATGTGTGT others(9): Show |
6 | a0001c0001t0020a0001c0001t0025a0001c0001t0030others(3): Show | 10 | HG01106.hp2 HG01515.hp2 HG01517.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1022_*1037dupCACA others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216327
|
A | ATGTGTGT others(19): Show |
9 | a0001c0001t0002a0001c0001t0018a0001c0001t0039others(6): Show | 44 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1037_*1038insCACA others(22): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216327
|
A | ATGTGTGT others(21): Show |
2 | a0001c0001t0017a0001c0001t0080 | 4 | HG02615.hp2 HG02683.hp1 HG04184.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1037_*1038insCACA others(24): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216327
|
A | ATGTGTGT others(23): Show |
1 | a0001c0001t0036 | 2 | NA18984.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1037_*1038insCACA others(26): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216327
|
A | ATGTGTGT others(11): Show |
15 | a0001c0001t0005a0001c0001t0012a0001c0001t0019others(12): Show | 33 | HG00140.hp2 HG00438.hp1 HG01361.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1020_*1037dupCACA others(14): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216327
|
A | ATGTGTGT others(13): Show |
16 | a0001c0001t0003a0001c0001t0006a0001c0001t0014others(13): Show | 50 | HG00544.hp1 HG01074.hp2 HG01081.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1018_*1037dupCACA others(16): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216327
|
A | ATGTGTGT others(15): Show |
12 | a0001c0001t0008a0001c0001t0009a0001c0001t0011others(9): Show | 35 | HG00408.hp2 HG00741.hp2 HG01069.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1016_*1037dupCACA others(18): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216327
|
A | ATGTGTGT others(17): Show |
14 | a0001c0001t0007a0001c0001t0013a0001c0001t0022others(11): Show | 31 | HG00099.hp2 HG00280.hp1 HG01099.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1014_*1037dupCACA others(20): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216327
|
A | ATGTGTGT others(19): Show |
4 | a0001c0001t0032a0001c0001t0038a0001c0001t0092others(1): Show | 6 | HG01109.hp1 HG01981.hp2 HG02257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1012_*1037dupCACA others(22): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216327
|
A | ATGTGTGT others(21): Show |
4 | a0001c0001t0016a0001c0001t0031a0001c0001t0040others(1): Show | 8 | HG00280.hp2 HG01074.hp1 HG01255.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1037_*1038insCACA others(24): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216327
|
A | ATGTGTGT others(23): Show |
1 | a0001c0001t0075 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1037_*1038insCACA others(26): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216327
|
A | ATGTGTGT others(25): Show |
2 | a0001c0001t0015a0001c0001t0091 | 4 | HG00738.hp1 HG00741.hp1 HG02572.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1037_*1038insCACA others(28): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216327
|
A | ATGTGTGT others(27): Show |
2 | a0001c0001t0067a0001c0001t0090 | 2 | HG01123.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1037_*1038insCACA others(30): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216327
|
A | ATGTGTGT others(37): Show |
1 | a0001c0001t0065 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1037_*1038insCACA others(40): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | |||||
chr9:36216367
|
G | A | 1 | a0001c0001t0064 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*998C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 998 | chr9 | 36216367 | |||||
chr9:36216428
|
C | G | 1 | a0001c0001t0095 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*937G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 937 | chr9 | 36216428 | |||||
chr9:36216428
|
C | T | 4 | a0001c0001t0084a0001c0001t0091a0001c0001t0092others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*937G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 937 | chr9 | 36216428 | |||||
chr9:36216429
|
G | A | 33 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(30): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*936C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 936 | chr9 | 36216429 | |||||
chr9:36216640
|
G | GATT | 5 | a0001c0001t0010a0001c0001t0038a0001c0001t0039others(2): Show | 15 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*722_*724dupAAT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 724 | chr9 | 36216640 | |||||
chr9:36216640
|
G | GATTATT | 32 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(29): Show | 97 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*719_*724dupAATAAT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 724 | chr9 | 36216640 | |||||
chr9:36216640
|
G | GATTATTA others(2): Show |
11 | a0001c0001t0017a0001c0001t0018a0001c0001t0029others(8): Show | 17 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*716_*724dupAATAAT others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 724 | chr9 | 36216640 | |||||
chr9:36216640
|
G | GATTATTA others(5): Show |
4 | a0001c0001t0053a0001c0001t0070a0001c0001t0072others(1): Show | 4 | HG01175.hp2 HG03834.hp2 HG03942.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*713_*724dupAATAAT others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 724 | chr9 | 36216640 | |||||
chr9:36216640
|
GATT | G | 5 | a0001c0001t0042a0001c0001t0050a0001c0001t0091others(2): Show | 6 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*722_*724delAAT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 722 | chr9 | 36216640 | |||||
chr9:36216640
|
GATTATTA others(2): Show |
G | 4 | a0001c0001t0014a0001c0001t0043a0001c0001t0044others(1): Show | 10 | HG01074.hp2 HG02280.hp1 HG02723.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*716_*724delAATAAT others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 716 | chr9 | 36216640 | |||||
chr9:36216663
|
TTATTATT others(5): Show |
T | 3 | a0001c0001t0067a0001c0001t0068a0001c0001t0069 | 3 | HG01123.hp2 HG03239.hp1 HG03490.hp2 |
3_prime_UTR_variant | MODIFIER | c.*690_*701delTAAATA others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 690 | chr9 | 36216663 | |||||
chr9:36216669
|
TTATTTA | T | 11 | a0001c0001t0007a0001c0001t0008a0001c0001t0012others(8): Show | 42 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*690_*695delTAAATA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 690 | chr9 | 36216669 | |||||
chr9:36216672
|
T | TTA | 3 | a0001c0001t0013a0001c0001t0054a0001c0001t0056 | 7 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*692_*693insTA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 692 | chr9 | 36216672 | |||||
chr9:36216672
|
TTTA | T | 9 | a0001c0001t0005a0001c0001t0006a0001c0001t0011others(6): Show | 40 | HG00140.hp2 HG00438.hp1 HG00741.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*690_*692delTAA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 690 | chr9 | 36216672 | |||||
chr9:36216674
|
T | A | 4 | a0001c0001t0057a0001c0001t0058a0001c0001t0059others(1): Show | 4 | HG01928.hp1 NA19030.hp2 NA20752.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*691A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 691 | chr9 | 36216674 | |||||
chr9:36216675
|
A | AT | 3 | a0001c0001t0052a0001c0001t0055a0001c0001t0056 | 3 | HG02486.hp2 HG03195.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*689dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 689 | chr9 | 36216675 | |||||
chr9:36216675
|
A | T | 4 | a0001c0001t0057a0001c0001t0058a0001c0001t0059others(1): Show | 4 | HG01928.hp1 NA19030.hp2 NA20752.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*690T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 690 | chr9 | 36216675 | |||||
chr9:36216678
|
A | AT | 2 | a0001c0001t0013a0001c0001t0054 | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*686dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 686 | chr9 | 36216678 | |||||
chr9:36216735
|
G | A | 8 | a0001c0001t0045a0001c0001t0046a0001c0001t0095others(5): Show | 10 | HG01109.hp1 HG01884.hp1 HG02622.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*630C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 630 | chr9 | 36216735 | |||||
chr9:36216782
|
C | T | 1 | a0001c0001t0053 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*583G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 583 | chr9 | 36216782 | |||||
chr9:36216914
|
C | T | 1 | a0001c0001t0052 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*451G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 451 | chr9 | 36216914 | |||||
chr9:36217012
|
C | T | 1 | a0001c0002t0051 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*353G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 353 | chr9 | 36217012 | |||||
chr9:36217082
|
CTAT | C | 1 | a0001c0001t0022 | 3 | HG00099.hp2 HG01099.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*280_*282delATA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 280 | chr9 | 36217082 | |||||
chr9:36217291
|
C | T | 6 | a0001c0001t0023a0001c0001t0048a0001c0001t0050others(3): Show | 7 | HG01884.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*74G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 74 | chr9 | 36217291 | |||||
chr9:36276954
|
C | T | 2 | a0001c0001t0012a0001c0001t0047 | 6 | HG02451.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-10G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/12 | chr9 | 36276954 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:36217801
|
G | A | 99 | a0001c0001t0005g0008a0001c0001t0005g0104a0001c0001t0005g0189others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.2027-201C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36217801 | ||||||
chr9:36217819
|
C | T | 1 | a0001c0001t0025g0217 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2027-219G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36217819 | ||||||
chr9:36217893
|
G | T | 1 | a0001c0001t0011g0192 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2026+290C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36217893 | ||||||
chr9:36218015
|
T | C | 1 | a0001c0001t0017g0078 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2026+168A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36218015 | ||||||
chr9:36218021
|
C | G | 241 | a0001c0001t0002g0076a0001c0001t0002g0079a0001c0001t0002g0080others(238): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.2026+162G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36218021 | ||||||
chr9:36218043
|
G | A | 1 | a0001c0001t0001g0335 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2026+140C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36218043 | ||||||
chr9:36218084
|
CT | C | 3 | a0001c0001t0091g0355a0001c0001t0092g0354a0001c0001t0093g0353 | 3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2026+98delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36218084 | ||||||
chr9:36218142
|
G | A | 1 | a0001c0001t0040g0348 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2026+41C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36218142 | ||||||
chr9:36218153
|
C | G | 1 | a0001c0001t0025g0195 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2026+30G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36218153 | ||||||
chr9:36218380
|
C | G | 44 | a0001c0001t0007g0140a0001c0001t0007g0142a0001c0001t0007g0154others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1910-81G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36218380 | ||||||
chr9:36218400
|
G | A | 1 | a0001c0001t0068g0173 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1910-101C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36218400 | ||||||
chr9:36218473
|
C | T | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1910-174G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36218473 | ||||||
chr9:36218525
|
C | T | 2 | a0001c0001t0037g0290a0001c0001t0037g0305 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1910-226G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36218525 | ||||||
chr9:36218575
|
C | T | 2 | a0001c0001t0007g0170a0001c0001t0007g0181 | 2 | NA18944.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1910-276G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36218575 | ||||||
chr9:36218967
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1910-668C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36218967 | ||||||
chr9:36219011
|
A | G | 7 | a0001c0001t0023g0236a0001c0001t0048g0073a0001c0001t0050g0074others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1910-712T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36219011 | ||||||
chr9:36219089
|
T | C | 1 | a0001c0001t0001g0339 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1909+749A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36219089 | ||||||
chr9:36219343
|
T | G | 1 | a0001c0001t0035g0067 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1909+495A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36219343 | ||||||
chr9:36219508
|
C | T | 2 | a0001c0001t0011g0211a0001c0001t0062g0210 | 2 | HG00741.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1909+330G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36219508 | ||||||
chr9:36219820
|
C | T | 1 | a0001c0002t0024g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1909+18G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36219820 | ||||||
chr9:36220027
|
C | T | 1 | a0001c0001t0001g0307 | 1 | NA18951.hp1 | splice_region_variant&intron_variant | LOW | c.1727-7G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36220027 | ||||||
chr9:36220137
|
T | C | 51 | a0001c0001t0003g0009a0001c0001t0003g0019a0001c0001t0003g0022others(48): Show | 52 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1727-117A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36220137 | ||||||
chr9:36220208
|
A | C | 1 | a0001c0001t0002g0122 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1727-188T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36220208 | ||||||
chr9:36220439
|
G | A | 252 | a0001c0001t0001g0114a0001c0001t0002g0076a0001c0001t0002g0079others(249): Show | 253 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1727-419C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36220439 | ||||||
chr9:36220848
|
T | C | 22 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0243others(19): Show | 22 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.1727-828A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36220848 | ||||||
chr9:36221039
|
G | A | 1 | a0001c0001t0004g0302 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1727-1019C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36221039 | ||||||
chr9:36221137
|
G | A | 242 | a0001c0001t0001g0114a0001c0001t0002g0076a0001c0001t0002g0079others(239): Show | 243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1727-1117C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36221137 | ||||||
chr9:36221148
|
T | G | 5 | a0001c0001t0013g0068a0001c0001t0013g0069a0001c0001t0013g0070others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1727-1128A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36221148 | ||||||
chr9:36221178
|
G | A | 52 | a0001c0001t0003g0009a0001c0001t0003g0019a0001c0001t0003g0022others(49): Show | 53 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.1727-1158C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36221178 | ||||||
chr9:36221337
|
G | T | 1 | a0001c0001t0014g0233 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1727-1317C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36221337 | ||||||
chr9:36221338
|
A | G | 1 | a0001c0001t0014g0233 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1727-1318T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36221338 | ||||||
chr9:36221974
|
C | T | 3 | a0001c0001t0012g0002a0001c0001t0012g0003a0001c0001t0012g0004 | 3 | HG02922.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1726+803G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36221974 | ||||||
chr9:36222144
|
C | T | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1726+633G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222144 | ||||||
chr9:36222146
|
C | T | 10 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0014g0083others(7): Show | 10 | HG01074.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1726+631G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222146 | ||||||
chr9:36222190
|
G | A | 3 | a0001c0001t0005g0206a0001c0001t0005g0220a0001c0001t0006g0215 | 3 | HG03927.hp2 NA19007.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1726+587C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222190 | ||||||
chr9:36222215
|
G | A | 2 | a0001c0001t0010g0286a0001c0001t0010g0289 | 2 | HG00639.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.1726+562C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222215 | ||||||
chr9:36222234
|
C | T | 1 | a0001c0001t0004g0340 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1726+543G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222234 | ||||||
chr9:36222235
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1726+542C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222235 | ||||||
chr9:36222262
|
A | G | 3 | a0001c0001t0012g0002a0001c0001t0012g0003a0001c0001t0012g0004 | 3 | HG02922.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1726+515T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222262 | ||||||
chr9:36222292
|
G | A | 135 | a0001c0001t0001g0114a0001c0001t0002g0082a0001c0001t0002g0093others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1726+485C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222292 | ||||||
chr9:36222346
|
G | A | 2 | a0001c0001t0011g0208a0001c0001t0011g0209 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1726+431C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222346 | ||||||
chr9:36222418
|
C | CA | 129 | a0001c0001t0001g0160a0001c0001t0001g0228a0001c0001t0001g0250others(126): Show | 129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1726+358dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222418 | ||||||
chr9:36222418
|
C | CAA | 19 | a0001c0001t0001g0114a0001c0001t0002g0082a0001c0001t0002g0094others(16): Show | 19 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1726+357_1726+358d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222418 | ||||||
chr9:36222418
|
CA | C | 60 | a0001c0001t0003g0009a0001c0001t0003g0019a0001c0001t0003g0022others(57): Show | 61 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.1726+358delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222418 | ||||||
chr9:36222436
|
C | A | 2 | a0001c0001t0002g0117a0001c0001t0083g0119 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1726+341G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222436 | ||||||
chr9:36222501
|
C | G | 1 | a0001c0001t0084g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1726+276G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222501 | ||||||
chr9:36222540
|
G | A | 39 | a0001c0001t0001g0114a0001c0001t0002g0082a0001c0001t0002g0093others(36): Show | 39 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1726+237C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222540 | ||||||
chr9:36222625
|
C | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0259 | 3 | NA18960.hp1 NA19086.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1726+152G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222625 | ||||||
chr9:36222652
|
C | G | 53 | a0001c0001t0003g0009a0001c0001t0003g0019a0001c0001t0003g0022others(50): Show | 54 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.1726+125G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222652 | ||||||
chr9:36222659
|
A | G | 6 | a0001c0001t0013g0068a0001c0001t0013g0069a0001c0001t0013g0070others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1726+118T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222659 | ||||||
chr9:36223002
|
C | T | 2 | a0001c0001t0008g0157a0001c0001t0016g0162 | 2 | NA18959.hp2 NA19084.hp2 |
splice_region_variant&intron_variant | LOW | c.1505-4G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 8/11 | chr9 | 36223002 | ||||||
chr9:36223269
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1504+104T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 8/11 | chr9 | 36223269 | ||||||
chr9:36223350
|
G | A | 1 | a0001c0001t0041g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1504+23C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 8/11 | chr9 | 36223350 | ||||||
chr9:36223657
|
G | A | 81 | a0001c0001t0001g0114a0001c0001t0002g0082a0001c0001t0002g0093others(78): Show | 81 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1375-155C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36223657 | ||||||
chr9:36223755
|
C | CT | 7 | a0001c0001t0013g0068a0001c0001t0013g0069a0001c0001t0013g0070others(4): Show | 7 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1375-254dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36223755 | ||||||
chr9:36223783
|
G | A | 51 | a0001c0001t0003g0009a0001c0001t0003g0019a0001c0001t0003g0022others(48): Show | 52 | HG00408.hp2 HG00544.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.1375-281C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36223783 | ||||||
chr9:36223804
|
C | T | 214 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0135others(211): Show | 215 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1375-302G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36223804 | ||||||
chr9:36223854
|
C | T | 11 | a0001c0001t0023g0236a0001c0001t0048g0073a0001c0001t0050g0074others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1375-352G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36223854 | ||||||
chr9:36223855
|
G | A | 7 | a0001c0001t0001g0081a0001c0001t0001g0311a0001c0001t0013g0068others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.1375-353C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36223855 | ||||||
chr9:36224048
|
G | A | 1 | a0001c0001t0003g0057 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1375-546C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224048 | ||||||
chr9:36224084
|
G | A | 2 | a0001c0001t0001g0291a0001c0001t0001g0296 | 2 | HG00140.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1375-582C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224084 | ||||||
chr9:36224165
|
G | A | 10 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0014g0083others(7): Show | 10 | HG01074.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1375-663C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224165 | ||||||
chr9:36224374
|
C | T | 45 | a0001c0001t0007g0140a0001c0001t0007g0142a0001c0001t0007g0154others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1375-872G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224374 | ||||||
chr9:36224591
|
G | A | 2 | a0001c0001t0042g0256a0001c0001t0042g0260 | 2 | HG01109.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1375-1089C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224591 | ||||||
chr9:36224609
|
C | T | 1 | a0001c0001t0085g0349 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1375-1107G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224609 | ||||||
chr9:36224681
|
G | A | 1 | a0001c0002t0049g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1375-1179C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224681 | ||||||
chr9:36224681
|
G | T | 1 | a0001c0001t0006g0185 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1375-1179C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224681 | ||||||
chr9:36224715
|
C | A | 1 | a0001c0002t0035g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1375-1213G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224715 | ||||||
chr9:36224724
|
G | T | 1 | a0001c0002t0035g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1375-1222C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224724 | ||||||
chr9:36224914
|
C | A | 3 | a0001c0001t0002g0116a0001c0001t0002g0136a0001c0001t0002g0269 | 3 | HG00639.hp2 HG00735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1375-1412G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224914 | ||||||
chr9:36225592
|
G | A | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1374+1656C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36225592 | ||||||
chr9:36225745
|
C | T | 1 | a0001c0001t0007g0161 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1374+1503G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36225745 | ||||||
chr9:36225785
|
A | T | 6 | a0001c0001t0012g0002a0001c0001t0012g0003a0001c0001t0012g0004others(3): Show | 6 | HG02451.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1374+1463T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36225785 | ||||||
chr9:36225902
|
ACT | A | 21 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0257others(18): Show | 21 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.1374+1344_1374+134 others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36225902 | ||||||
chr9:36226116
|
T | C | 3 | a0001c0001t0055g0345a0001c0001t0056g0344a0001c0001t0059g0343 | 3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1374+1132A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36226116 | ||||||
chr9:36226265
|
T | C | 4 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0320others(1): Show | 4 | HG02109.hp1 HG02717.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1374+983A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36226265 | ||||||
chr9:36226339
|
A | AT | 96 | a0001c0001t0001g0114a0001c0001t0001g0228a0001c0001t0001g0250others(93): Show | 96 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1374+908dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36226339 | ||||||
chr9:36226339
|
A | ATT | 46 | a0001c0001t0002g0107a0001c0001t0002g0136a0001c0001t0005g0214others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1374+907_1374+908d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36226339 | ||||||
chr9:36226431
|
A | T | 1 | a0001c0001t0035g0067 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1374+817T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36226431 | ||||||
chr9:36227188
|
T | TA | 8 | a0001c0001t0039g0138a0001c0001t0039g0139a0001c0001t0044g0342others(5): Show | 8 | HG02280.hp1 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1374+59dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36227188 | ||||||
chr9:36227204
|
C | T | 11 | a0001c0001t0023g0236a0001c0001t0048g0073a0001c0001t0050g0074others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1374+44G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36227204 | ||||||
chr9:36227221
|
A | G | 1 | a0001c0001t0080g0124 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1374+27T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36227221 | ||||||
chr9:36227633
|
G | T | 3 | a0001c0001t0039g0138a0001c0001t0039g0139a0001c0001t0070g0047 | 3 | HG02572.hp2 HG03098.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1164-175C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36227633 | ||||||
chr9:36227811
|
G | A | 1 | a0001c0001t0015g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1164-353C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36227811 | ||||||
chr9:36228032
|
C | CA | 23 | a0001c0001t0001g0056a0001c0001t0001g0241a0001c0001t0001g0252others(20): Show | 23 | HG00735.hp1 HG01069.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.1164-575dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228032 | ||||||
chr9:36228051
|
AC | A | 9 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(6): Show | 9 | HG01255.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1164-594delG | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228051 | ||||||
chr9:36228052
|
C | A | 3 | a0001c0001t0039g0138a0001c0001t0039g0139a0001c0001t0056g0344 | 3 | HG02572.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1164-594G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228052 | ||||||
chr9:36228283
|
CTT | C | 6 | a0001c0001t0012g0002a0001c0001t0012g0003a0001c0001t0012g0004others(3): Show | 6 | HG02451.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1163+736_1163+737d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228283 | ||||||
chr9:36228425
|
T | G | 2 | a0001c0001t0037g0290a0001c0001t0037g0305 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1163+596A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228425 | ||||||
chr9:36228567
|
C | A | 45 | a0001c0001t0007g0140a0001c0001t0007g0142a0001c0001t0007g0154others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1163+454G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228567 | ||||||
chr9:36228716
|
C | T | 3 | a0001c0001t0002g0108a0001c0001t0002g0121a0001c0001t0002g0122 | 3 | NA19060.hp2 NA19064.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1163+305G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228716 | ||||||
chr9:36228750
|
C | T | 1 | a0001c0001t0007g0170 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1163+271G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228750 | ||||||
chr9:36228759
|
A | G | 1 | a0001c0001t0014g0233 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1163+262T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228759 | ||||||
chr9:36228793
|
C | CA | 41 | a0001c0001t0001g0250a0001c0001t0002g0101a0001c0001t0007g0140others(38): Show | 41 | HG00280.hp1 HG00738.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1163+227dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228793 | ||||||
chr9:36228793
|
CA | C | 43 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0326others(40): Show | 43 | HG00544.hp2 HG01074.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1163+227delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228793 | ||||||
chr9:36228793
|
CAA | C | 40 | a0001c0001t0003g0009a0001c0001t0003g0019a0001c0001t0003g0022others(37): Show | 41 | HG00408.hp2 HG00544.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.1163+226_1163+227d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228793 | ||||||
chr9:36229260
|
T | C | 2 | a0002c0003t0009g0188a0002c0003t0033g0186 | 2 | NA18951.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1076-152A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36229260 | ||||||
chr9:36229381
|
C | T | 22 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0014g0083others(19): Show | 22 | HG01074.hp2 HG01255.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1076-273G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36229381 | ||||||
chr9:36229599
|
T | G | 241 | a0001c0001t0001g0114a0001c0001t0002g0076a0001c0001t0002g0079others(238): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1076-491A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36229599 | ||||||
chr9:36229712
|
A | G | 10 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0014g0083others(7): Show | 10 | HG01074.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1076-604T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36229712 | ||||||
chr9:36229821
|
A | G | 3 | a0001c0001t0055g0345a0001c0001t0056g0344a0001c0001t0059g0343 | 3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1076-713T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36229821 | ||||||
chr9:36229885
|
C | T | 1 | a0001c0001t0067g0144 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1076-777G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36229885 | ||||||
chr9:36229920
|
C | T | 1 | a0001c0001t0022g0164 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1076-812G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36229920 | ||||||
chr9:36229952
|
C | CT | 8 | a0001c0001t0001g0308a0001c0001t0002g0117a0001c0001t0013g0068others(5): Show | 8 | HG00621.hp1 HG01243.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1076-845dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36229952 | ||||||
chr9:36230011
|
A | G | 1 | a0001c0001t0073g0297 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1076-903T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36230011 | ||||||
chr9:36230082
|
G | A | 3 | a0001c0001t0007g0140a0001c0001t0007g0161a0001c0001t0008g0201 | 3 | HG01943.hp1 HG01975.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1076-974C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36230082 | ||||||
chr9:36230371
|
C | A | 1 | a0001c0001t0002g0111 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1076-1263G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36230371 | ||||||
chr9:36230483
|
G | T | 4 | a0001c0001t0005g0199a0001c0001t0006g0197a0001c0001t0058g0205others(1): Show | 4 | HG01192.hp1 HG01928.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076-1375C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36230483 | ||||||
chr9:36230619
|
C | A | 1 | a0001c0001t0023g0236 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1076-1511G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36230619 | ||||||
chr9:36230660
|
CT | C | 6 | a0001c0001t0001g0299a0001c0001t0002g0096a0001c0001t0002g0107others(3): Show | 6 | HG01099.hp2 HG01167.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1076-1553delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36230660 | ||||||
chr9:36230682
|
C | T | 2 | a0001c0001t0006g0066a0001c0001t0011g0352 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1076-1574G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36230682 | ||||||
chr9:36231066
|
T | TAAAA | 47 | a0001c0001t0003g0009a0001c0001t0003g0019a0001c0001t0003g0029others(44): Show | 48 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1076-1962_1076-195 others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231066 | ||||||
chr9:36231066
|
T | TAAAAA | 12 | a0001c0001t0023g0236a0001c0001t0045g0010a0001c0001t0048g0073others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1076-1963_1076-195 others(9): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231066 | ||||||
chr9:36231066
|
TA | T | 14 | a0001c0001t0001g0246a0001c0001t0001g0267a0001c0001t0001g0298others(11): Show | 14 | HG01943.hp2 HG01975.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.1076-1959delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231066 | ||||||
chr9:36231081
|
A | AAAG | 15 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0014g0083others(12): Show | 15 | HG01074.hp2 HG01255.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1076-1974_1076-197 others(7): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231081 | ||||||
chr9:36231081
|
A | G | 2 | a0001c0001t0044g0342a0001c0001t0044g0346 | 2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1076-1973T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231081 | ||||||
chr9:36231084
|
AG | A | 3 | a0001c0001t0091g0355a0001c0001t0092g0354a0001c0001t0093g0353 | 3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1076-1977delC | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231084 | ||||||
chr9:36231085
|
G | A | 15 | a0001c0001t0002g0076a0001c0001t0002g0079a0001c0001t0002g0080others(12): Show | 15 | HG00280.hp2 HG01074.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.1076-1977C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231085 | ||||||
chr9:36231089
|
G | A | 4 | a0001c0001t0030g0312a0001c0001t0030g0313a0001c0001t0034g0092others(1): Show | 4 | HG01257.hp2 HG03669.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076-1981C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231089 | ||||||
chr9:36231089
|
GAA | G | 3 | a0001c0001t0001g0295a0001c0001t0007g0174a0001c0001t0007g0176 | 3 | HG01257.hp1 HG01258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1076-1983_1076-198 others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231089 | ||||||
chr9:36231091
|
AAGAG | A | 13 | a0001c0001t0002g0076a0001c0001t0002g0079a0001c0001t0002g0080others(10): Show | 13 | HG00280.hp2 HG01074.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.1076-1987_1076-198 others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231091 | ||||||
chr9:36231095
|
G | A | 4 | a0001c0001t0030g0312a0001c0001t0030g0313a0001c0001t0034g0092others(1): Show | 4 | HG01257.hp2 HG03669.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076-1987C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231095 | ||||||
chr9:36231123
|
CAATG | C | 241 | a0001c0001t0001g0114a0001c0001t0002g0076a0001c0001t0002g0079others(238): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1076-2019_1076-201 others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231123 | ||||||
chr9:36231134
|
G | A | 241 | a0001c0001t0001g0114a0001c0001t0002g0076a0001c0001t0002g0079others(238): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1076-2026C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231134 | ||||||
chr9:36231274
|
G | A | 1 | a0001c0001t0004g0249 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1076-2166C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231274 | ||||||
chr9:36231414
|
C | T | 1 | a0001c0001t0091g0355 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1076-2306G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231414 | ||||||
chr9:36231486
|
T | C | 241 | a0001c0001t0001g0114a0001c0001t0002g0076a0001c0001t0002g0079others(238): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1076-2378A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231486 | ||||||
chr9:36231488
|
C | T | 1 | a0001c0001t0034g0092 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1076-2380G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231488 | ||||||
chr9:36231801
|
A | G | 10 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0014g0083others(7): Show | 10 | HG01074.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1075+2119T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231801 | ||||||
chr9:36231930
|
A | G | 1 | a0001c0001t0008g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1075+1990T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231930 | ||||||
chr9:36231970
|
C | T | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1075+1950G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231970 | ||||||
chr9:36232196
|
A | T | 1 | a0001c0001t0017g0078 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1075+1724T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232196 | ||||||
chr9:36232222
|
C | T | 5 | a0001c0001t0010g0288a0001c0001t0038g0351a0001c0001t0040g0348others(2): Show | 5 | HG00099.hp1 HG01255.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075+1698G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232222 | ||||||
chr9:36232328
|
G | GC | 12 | a0001c0001t0001g0258a0001c0001t0001g0275a0001c0001t0001g0339others(9): Show | 12 | HG00735.hp2 HG01928.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.1075+1591dupG | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232328 | ||||||
chr9:36232328
|
GC | G | 14 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1075+1591delG | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232328 | ||||||
chr9:36232331
|
C | G | 147 | a0001c0001t0001g0114a0001c0001t0001g0158a0001c0001t0001g0159others(144): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1075+1589G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232331 | ||||||
chr9:36232332
|
C | G | 15 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1075+1588G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232332 | ||||||
chr9:36232332
|
CCCCGCCC others(5): Show |
C | 56 | a0001c0001t0001g0056a0001c0001t0001g0303a0001c0001t0001g0304others(53): Show | 57 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.1075+1576_1075+158 others(16): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232332 | ||||||
chr9:36232334
|
CCGCCCCC others(3): Show |
C | 1 | a0001c0001t0001g0257 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1075+1576_1075+158 others(14): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232334 | ||||||
chr9:36232335
|
C | A | 2 | a0001c0001t0008g0152a0001c0001t0066g0180 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1075+1585G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232335 | ||||||
chr9:36232336
|
G | A | 14 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1075+1584C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232336 | ||||||
chr9:36232336
|
G | C | 2 | a0001c0001t0008g0152a0001c0001t0066g0180 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1075+1584C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232336 | ||||||
chr9:36232338
|
C | G | 2 | a0001c0001t0042g0256a0001c0001t0042g0260 | 2 | HG01109.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1075+1582G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232338 | ||||||
chr9:36232340
|
C | A | 5 | a0001c0001t0039g0138a0001c0001t0039g0139a0001c0001t0055g0345others(2): Show | 5 | HG02572.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075+1580G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232340 | ||||||
chr9:36232341
|
C | G | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+1579G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232341 | ||||||
chr9:36232343
|
CT | C | 5 | a0001c0001t0039g0138a0001c0001t0039g0139a0001c0001t0055g0345others(2): Show | 5 | HG02572.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075+1576delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232343 | ||||||
chr9:36232344
|
T | C | 147 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0227others(144): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1075+1576A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232344 | ||||||
chr9:36232345
|
C | A | 106 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0227others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.1075+1575G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232345 | ||||||
chr9:36232345
|
C | CA | 35 | a0001c0001t0001g0258a0001c0001t0001g0261a0001c0001t0001g0275others(32): Show | 35 | HG00544.hp2 HG00609.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1075+1574_1075+157 others(5): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232345 | ||||||
chr9:36232416
|
T | C | 178 | a0001c0001t0001g0114a0001c0001t0001g0158a0001c0001t0001g0159others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1075+1504A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232416 | ||||||
chr9:36232548
|
C | T | 7 | a0001c0001t0048g0073a0001c0001t0050g0074a0001c0002t0023g0026others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075+1372G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232548 | ||||||
chr9:36232700
|
C | T | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+1220G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232700 | ||||||
chr9:36232723
|
C | G | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+1197G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232723 | ||||||
chr9:36232869
|
A | T | 1 | a0001c0001t0001g0307 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1075+1051T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232869 | ||||||
chr9:36232997
|
C | G | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+923G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232997 | ||||||
chr9:36233061
|
C | T | 53 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(50): Show | 54 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.1075+859G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233061 | ||||||
chr9:36233241
|
G | A | 3 | a0001c0001t0012g0002a0001c0001t0012g0003a0001c0001t0012g0004 | 3 | HG02922.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1075+679C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233241 | ||||||
chr9:36233260
|
T | C | 1 | a0001c0001t0087g0232 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1075+660A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233260 | ||||||
chr9:36233289
|
C | T | 13 | a0001c0001t0014g0233a0001c0001t0014g0237a0001c0001t0023g0236others(10): Show | 13 | HG02280.hp1 HG02486.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1075+631G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233289 | ||||||
chr9:36233392
|
C | T | 1 | a0001c0001t0035g0067 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1075+528G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233392 | ||||||
chr9:36233432
|
C | T | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+488G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233432 | ||||||
chr9:36233441
|
C | T | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+479G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233441 | ||||||
chr9:36233484
|
G | A | 1 | a0001c0001t0004g0249 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1075+436C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233484 | ||||||
chr9:36233552
|
A | G | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1075+368T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233552 | ||||||
chr9:36233666
|
CA | C | 238 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(235): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1075+253delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233666 | ||||||
chr9:36233673
|
A | C | 22 | a0001c0001t0001g0081a0001c0001t0002g0076a0001c0001t0002g0079others(19): Show | 22 | HG00280.hp2 HG01074.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1075+247T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233673 | ||||||
chr9:36234247
|
T | C | 1 | a0001c0001t0003g0034 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.863-115A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36234247 | ||||||
chr9:36234442
|
G | T | 53 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(50): Show | 54 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.863-310C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36234442 | ||||||
chr9:36234611
|
A | G | 1 | a0001c0001t0083g0119 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.863-479T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36234611 | ||||||
chr9:36234700
|
C | T | 1 | a0001c0001t0048g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.863-568G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36234700 | ||||||
chr9:36234939
|
C | T | 5 | a0001c0001t0005g0202a0001c0001t0005g0204a0001c0001t0005g0207others(2): Show | 5 | HG00438.hp1 HG01981.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.863-807G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36234939 | ||||||
chr9:36235077
|
A | C | 9 | a0001c0001t0045g0010a0001c0001t0045g0018a0001c0001t0046g0014others(6): Show | 9 | HG01109.hp1 HG02622.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.863-945T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235077 | ||||||
chr9:36235129
|
C | T | 3 | a0001c0001t0002g0108a0001c0001t0002g0121a0001c0001t0002g0122 | 3 | NA19060.hp2 NA19064.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.863-997G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235129 | ||||||
chr9:36235151
|
G | T | 1 | a0001c0001t0015g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.863-1019C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235151 | ||||||
chr9:36235190
|
C | T | 232 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(229): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.863-1058G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235190 | ||||||
chr9:36235308
|
G | A | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.863-1176C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235308 | ||||||
chr9:36235506
|
T | G | 6 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0275others(3): Show | 6 | HG02056.hp2 NA18946.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.862+1326A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235506 | ||||||
chr9:36235541
|
T | C | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.862+1291A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235541 | ||||||
chr9:36235624
|
A | C | 139 | a0001c0001t0001g0114a0001c0001t0001g0158a0001c0001t0001g0159others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.862+1208T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235624 | ||||||
chr9:36235769
|
G | A | 1 | a0001c0001t0060g0191 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.862+1063C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235769 | ||||||
chr9:36235779
|
C | G | 4 | a0001c0001t0084g0089a0001c0001t0091g0355a0001c0001t0092g0354others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.862+1053G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235779 | ||||||
chr9:36235791
|
G | A | 10 | a0001c0001t0048g0073a0001c0001t0050g0074a0001c0002t0018g0023others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.862+1041C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235791 | ||||||
chr9:36235884
|
T | C | 4 | a0001c0001t0007g0174a0001c0001t0007g0176a0001c0001t0008g0175others(1): Show | 4 | HG01175.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.862+948A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235884 | ||||||
chr9:36236070
|
G | A | 2 | a0001c0001t0030g0312a0001c0001t0030g0313 | 2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.862+762C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36236070 | ||||||
chr9:36236200
|
C | A | 4 | a0001c0001t0084g0089a0001c0001t0091g0355a0001c0001t0092g0354others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.862+632G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36236200 | ||||||
chr9:36236206
|
C | CT | 11 | a0001c0001t0001g0243a0001c0001t0001g0246a0001c0001t0001g0247others(8): Show | 11 | HG02027.hp1 HG02027.hp2 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.862+625dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36236206 | ||||||
chr9:36236497
|
A | G | 232 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(229): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.862+335T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36236497 | ||||||
chr9:36236636
|
T | C | 1 | a0001c0001t0002g0120 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.862+196A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36236636 | ||||||
chr9:36237244
|
T | G | 5 | a0001c0001t0014g0233a0001c0001t0014g0237a0001c0001t0023g0236others(2): Show | 5 | HG02965.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.710-260A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237244 | ||||||
chr9:36237282
|
A | G | 10 | a0001c0001t0048g0073a0001c0001t0050g0074a0001c0002t0018g0023others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.710-298T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237282 | ||||||
chr9:36237489
|
AG | A | 3 | a0001c0001t0091g0355a0001c0001t0092g0354a0001c0001t0093g0353 | 3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.710-506delC | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237489 | ||||||
chr9:36237525
|
G | A | 2 | a0001c0001t0030g0312a0001c0001t0030g0313 | 2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.710-541C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237525 | ||||||
chr9:36237525
|
G | C | 1 | a0001c0001t0084g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.710-541C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237525 | ||||||
chr9:36237645
|
C | CT | 44 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0163others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.710-662dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237645 | ||||||
chr9:36237654
|
T | TA | 26 | a0001c0001t0001g0114a0001c0001t0002g0093a0001c0001t0002g0094others(23): Show | 26 | HG00621.hp2 HG01106.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.710-671_710-670ins others(1): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237654 | ||||||
chr9:36237655
|
T | A | 30 | a0001c0001t0001g0114a0001c0001t0002g0093a0001c0001t0002g0094others(27): Show | 30 | HG00621.hp2 HG01106.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.710-671A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237655 | ||||||
chr9:36237655
|
T | TA | 64 | a0001c0001t0002g0097a0001c0001t0002g0115a0001c0001t0002g0116others(61): Show | 64 | HG00140.hp2 HG00438.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.710-672dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237655 | ||||||
chr9:36237806
|
C | T | 1 | a0001c0001t0017g0078 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.710-822G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237806 | ||||||
chr9:36237861
|
C | A | 13 | a0001c0001t0014g0233a0001c0001t0014g0237a0001c0001t0023g0236others(10): Show | 13 | HG02280.hp1 HG02486.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.710-877G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237861 | ||||||
chr9:36237997
|
CT | C | 3 | a0001c0001t0036g0127a0001c0001t0044g0342a0001c0001t0044g0346 | 3 | HG02280.hp1 NA18984.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.710-1014delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237997 | ||||||
chr9:36238071
|
TAC | T | 52 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(49): Show | 53 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.710-1089_710-1088d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238071 | ||||||
chr9:36238123
|
T | TAC | 16 | a0001c0001t0001g0278a0001c0001t0003g0054a0001c0001t0030g0313others(13): Show | 16 | HG00438.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.710-1141_710-1140d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238123 | ||||||
chr9:36238123
|
T | TACAC | 5 | a0001c0001t0003g0042a0001c0001t0038g0351a0001c0001t0040g0348others(2): Show | 5 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.710-1143_710-1140d others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238123 | ||||||
chr9:36238123
|
T | TACACAC | 52 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(49): Show | 53 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.710-1145_710-1140d others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238123 | ||||||
chr9:36238123
|
TAC | T | 26 | a0001c0001t0001g0081a0001c0001t0002g0076a0001c0001t0002g0079others(23): Show | 26 | HG00280.hp2 HG01074.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.710-1141_710-1140d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238123 | ||||||
chr9:36238145
|
C | CAT | 138 | a0001c0001t0001g0114a0001c0001t0001g0158a0001c0001t0001g0159others(135): Show | 138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.710-1163_710-1162d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238145 | ||||||
chr9:36238145
|
C | T | 2 | a0001c0001t0006g0224a0001c0001t0006g0225 | 2 | HG01081.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.710-1161G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238145 | ||||||
chr9:36238219
|
A | G | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.710-1235T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238219 | ||||||
chr9:36238227
|
T | C | 1 | a0001c0001t0001g0332 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.710-1243A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238227 | ||||||
chr9:36238246
|
C | T | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.710-1262G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238246 | ||||||
chr9:36238247
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.710-1263C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238247 | ||||||
chr9:36238327
|
A | AGTTCTAC others(27): Show |
4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.710-1344_710-1343i others(36): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238327 | ||||||
chr9:36238521
|
A | G | 1 | a0001c0001t0005g0008 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.710-1537T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238521 | ||||||
chr9:36238529
|
T | G | 2 | a0001c0001t0006g0224a0001c0001t0006g0225 | 2 | HG01081.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.710-1545A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238529 | ||||||
chr9:36238633
|
G | T | 2 | a0001c0001t0039g0138a0001c0001t0039g0139 | 2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.710-1649C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238633 | ||||||
chr9:36238719
|
G | C | 1 | a0001c0001t0003g0034 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.710-1735C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238719 | ||||||
chr9:36238989
|
T | C | 10 | a0001c0001t0048g0073a0001c0001t0050g0074a0001c0002t0018g0023others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.710-2005A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238989 | ||||||
chr9:36239339
|
A | G | 1 | a0001c0001t0002g0120 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.710-2355T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36239339 | ||||||
chr9:36239414
|
T | C | 1 | a0001c0001t0079g0123 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.710-2430A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36239414 | ||||||
chr9:36239448
|
T | G | 2 | a0001c0001t0001g0291a0001c0001t0001g0296 | 2 | HG00140.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.710-2464A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36239448 | ||||||
chr9:36239663
|
G | C | 1 | a0001c0001t0045g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.710-2679C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36239663 | ||||||
chr9:36239720
|
G | A | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.710-2736C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36239720 | ||||||
chr9:36239726
|
G | A | 2 | a0001c0001t0008g0152a0001c0001t0066g0180 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.710-2742C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36239726 | ||||||
chr9:36239730
|
C | T | 1 | a0001c0001t0008g0169 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.710-2746G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36239730 | ||||||
chr9:36239754
|
T | C | 1 | a0001c0001t0067g0144 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.710-2770A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36239754 | ||||||
chr9:36240101
|
T | C | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.710-3117A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240101 | ||||||
chr9:36240120
|
T | C | 1 | a0001c0002t0023g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.710-3136A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240120 | ||||||
chr9:36240234
|
G | C | 3 | a0001c0001t0055g0345a0001c0001t0056g0344a0001c0001t0059g0343 | 3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.710-3250C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240234 | ||||||
chr9:36240240
|
A | G | 5 | a0001c0001t0014g0233a0001c0001t0014g0237a0001c0001t0023g0236others(2): Show | 5 | HG02965.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.710-3256T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240240 | ||||||
chr9:36240448
|
C | G | 240 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(237): Show | 241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.710-3464G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240448 | ||||||
chr9:36240519
|
A | T | 232 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(229): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.710-3535T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240519 | ||||||
chr9:36240732
|
ATTC | A | 3 | a0001c0001t0091g0355a0001c0001t0092g0354a0001c0001t0093g0353 | 3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.710-3751_710-3749d others(5): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240732 | ||||||
chr9:36240786
|
T | C | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | NA18943.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.710-3802A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240786 | ||||||
chr9:36240807
|
A | T | 10 | a0001c0001t0048g0073a0001c0001t0050g0074a0001c0002t0018g0023others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.710-3823T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240807 | ||||||
chr9:36241119
|
C | CT | 60 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(57): Show | 61 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.710-4136dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241119 | ||||||
chr9:36241254
|
T | C | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.710-4270A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241254 | ||||||
chr9:36241272
|
C | T | 1 | a0001c0001t0002g0129 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.710-4288G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241272 | ||||||
chr9:36241438
|
T | A | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.710-4454A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241438 | ||||||
chr9:36241525
|
G | T | 80 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(77): Show | 81 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.709+4506C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241525 | ||||||
chr9:36241603
|
A | G | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.709+4428T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241603 | ||||||
chr9:36241714
|
A | C | 1 | a0001c0001t0084g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.709+4317T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241714 | ||||||
chr9:36241755
|
T | C | 1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.709+4276A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241755 | ||||||
chr9:36241773
|
A | G | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.709+4258T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241773 | ||||||
chr9:36241857
|
C | G | 2 | a0001c0001t0044g0342a0001c0001t0044g0346 | 2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.709+4174G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241857 | ||||||
chr9:36242046
|
G | A | 2 | a0001c0001t0029g0118a0001c0001t0077g0125 | 2 | HG02738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.709+3985C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242046 | ||||||
chr9:36242090
|
T | C | 1 | a0001c0001t0087g0232 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.709+3941A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242090 | ||||||
chr9:36242164
|
GA | G | 164 | a0001c0001t0001g0081a0001c0001t0001g0114a0001c0001t0001g0158others(161): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.709+3866delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242164 | ||||||
chr9:36242281
|
A | T | 1 | a0001c0001t0008g0143 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.709+3750T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242281 | ||||||
chr9:36242287
|
C | CA | 145 | a0001c0001t0001g0081a0001c0001t0001g0114a0001c0001t0001g0158others(142): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.709+3743dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242287 | ||||||
chr9:36242312
|
T | C | 57 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(54): Show | 58 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.709+3719A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242312 | ||||||
chr9:36242327
|
C | T | 3 | a0001c0001t0001g0160a0001c0001t0008g0157a0001c0001t0016g0162 | 3 | NA18959.hp2 NA18988.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.709+3704G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242327 | ||||||
chr9:36242400
|
A | G | 1 | a0001c0002t0051g0341 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.709+3631T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242400 | ||||||
chr9:36242514
|
G | A | 3 | a0001c0001t0091g0355a0001c0001t0092g0354a0001c0001t0093g0353 | 3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.709+3517C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242514 | ||||||
chr9:36242564
|
T | C | 346 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(343): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.709+3467A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242564 | ||||||
chr9:36242665
|
G | A | 40 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.709+3366C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242665 | ||||||
chr9:36242667
|
C | T | 3 | a0001c0001t0091g0355a0001c0001t0092g0354a0001c0001t0093g0353 | 3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.709+3364G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242667 | ||||||
chr9:36242684
|
C | T | 1 | a0001c0001t0002g0129 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.709+3347G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242684 | ||||||
chr9:36242730
|
TTG | T | 7 | a0001c0001t0045g0018a0001c0001t0046g0014a0001c0001t0046g0015others(4): Show | 7 | HG02622.hp1 HG02818.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.709+3299_709+3300d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242730 | ||||||
chr9:36242732
|
G | GC | 4 | a0001c0001t0007g0142a0001c0001t0007g0154a0001c0001t0008g0175others(1): Show | 4 | HG01175.hp1 HG02135.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.709+3298_709+3299i others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242732 | ||||||
chr9:36242732
|
G | GT | 13 | a0001c0001t0001g0250a0001c0001t0001g0268a0001c0001t0001g0294others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.709+3298dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242732 | ||||||
chr9:36242732
|
G | GTTTTTTT others(40): Show |
1 | a0001c0001t0001g0293 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.709+3298_709+3299i others(49): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242732 | ||||||
chr9:36242732
|
G | T | 1 | a0001c0001t0045g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.709+3299C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242732 | ||||||
chr9:36242732
|
GT | G | 105 | a0001c0001t0001g0081a0001c0001t0001g0114a0001c0001t0002g0082others(102): Show | 105 | HG00140.hp2 HG00438.hp1 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.709+3298delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242732 | ||||||
chr9:36242732
|
GTT | G | 63 | a0001c0001t0001g0056a0001c0001t0002g0076a0001c0001t0002g0079others(60): Show | 64 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.709+3297_709+3298d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242732 | ||||||
chr9:36242733
|
T | C | 53 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(50): Show | 53 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.709+3298A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242733 | ||||||
chr9:36242734
|
T | C | 82 | a0001c0001t0001g0081a0001c0001t0001g0114a0001c0001t0002g0093others(79): Show | 82 | HG00140.hp2 HG00438.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.709+3297A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242734 | ||||||
chr9:36242735
|
T | C | 1 | a0001c0001t0062g0210 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.709+3296A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242735 | ||||||
chr9:36242826
|
C | T | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.709+3205G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242826 | ||||||
chr9:36242921
|
C | G | 232 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(229): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.709+3110G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242921 | ||||||
chr9:36243029
|
TG | T | 7 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(4): Show | 7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.709+3001delC | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36243029 | ||||||
chr9:36243336
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.709+2695G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36243336 | ||||||
chr9:36243449
|
G | A | 2 | a0001c0001t0001g0293a0001c0001t0004g0279 | 2 | HG02293.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.709+2582C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36243449 | ||||||
chr9:36243708
|
G | A | 1 | a0001c0001t0084g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.709+2323C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36243708 | ||||||
chr9:36243934
|
G | GT | 57 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(54): Show | 57 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.709+2096dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36243934 | ||||||
chr9:36243958
|
GT | G | 245 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(242): Show | 246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.709+2072delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36243958 | ||||||
chr9:36243967
|
T | G | 1 | a0001c0001t0031g0128 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.709+2064A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36243967 | ||||||
chr9:36244166
|
G | A | 2 | a0001c0001t0039g0138a0001c0001t0039g0139 | 2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.709+1865C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244166 | ||||||
chr9:36244246
|
G | A | 225 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(222): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.709+1785C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244246 | ||||||
chr9:36244399
|
T | A | 139 | a0001c0001t0001g0114a0001c0001t0001g0158a0001c0001t0001g0159others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.709+1632A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244399 | ||||||
chr9:36244582
|
T | C | 84 | a0001c0001t0001g0114a0001c0001t0002g0093a0001c0001t0002g0094others(81): Show | 84 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.709+1449A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244582 | ||||||
chr9:36244703
|
C | T | 7 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(4): Show | 7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.709+1328G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244703 | ||||||
chr9:36244727
|
G | A | 5 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0002g0120others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.709+1304C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244727 | ||||||
chr9:36244781
|
C | CA | 5 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0002g0120others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.709+1249dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244781 | ||||||
chr9:36244864
|
C | T | 1 | a0001c0001t0007g0142 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.709+1167G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244864 | ||||||
chr9:36244939
|
C | CA | 9 | a0001c0001t0001g0247a0001c0001t0001g0292a0001c0001t0002g0133others(6): Show | 9 | HG02071.hp2 HG02074.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.709+1091dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244939 | ||||||
chr9:36244939
|
CA | C | 16 | a0001c0001t0002g0082a0001c0001t0014g0233a0001c0001t0014g0237others(13): Show | 16 | HG01255.hp1 HG02280.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.709+1091delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244939 | ||||||
chr9:36244939
|
CAA | C | 6 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0085g0349others(3): Show | 6 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+1090_709+1091d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244939 | ||||||
chr9:36245179
|
G | A | 7 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(4): Show | 7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.709+852C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245179 | ||||||
chr9:36245205
|
A | G | 6 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0014g0083others(3): Show | 6 | HG01074.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+826T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245205 | ||||||
chr9:36245219
|
G | A | 3 | a0001c0001t0019g0051a0001c0001t0019g0064a0001c0001t0019g0065 | 3 | HG01978.hp1 HG01993.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.709+812C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245219 | ||||||
chr9:36245229
|
A | C | 4 | a0001c0001t0001g0135a0001c0001t0001g0261a0001c0001t0001g0278others(1): Show | 4 | HG00438.hp2 HG00621.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.709+802T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245229 | ||||||
chr9:36245404
|
G | T | 5 | a0001c0001t0014g0233a0001c0001t0014g0237a0001c0001t0023g0236others(2): Show | 5 | HG02965.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.709+627C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245404 | ||||||
chr9:36245460
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.709+571C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245460 | ||||||
chr9:36245574
|
T | A | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.709+457A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245574 | ||||||
chr9:36245762
|
A | G | 39 | a0001c0001t0001g0114a0001c0001t0002g0093a0001c0001t0002g0094others(36): Show | 39 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.709+269T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245762 | ||||||
chr9:36245887
|
A | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.709+144T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245887 | ||||||
chr9:36246560
|
C | T | 7 | a0001c0001t0039g0138a0001c0001t0039g0139a0001c0001t0044g0342others(4): Show | 7 | HG02280.hp1 HG02572.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-78G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246560 | ||||||
chr9:36246597
|
T | C | 139 | a0001c0001t0001g0114a0001c0001t0001g0158a0001c0001t0001g0159others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.258-115A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246597 | ||||||
chr9:36246660
|
C | CT | 15 | a0001c0001t0001g0247a0001c0001t0001g0254a0001c0001t0001g0255others(12): Show | 15 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.258-179dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246660 | ||||||
chr9:36246660
|
CT | C | 41 | a0001c0001t0001g0309a0001c0001t0002g0079a0001c0001t0002g0080others(38): Show | 41 | HG00280.hp2 HG01074.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.258-179delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246660 | ||||||
chr9:36246660
|
CTT | C | 6 | a0001c0001t0044g0342a0001c0001t0044g0346a0001c0001t0052g0347others(3): Show | 6 | HG02280.hp1 HG02486.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.258-180_258-179del others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246660 | ||||||
chr9:36246660
|
CTTT | C | 6 | a0001c0001t0038g0351a0001c0001t0039g0138a0001c0001t0039g0139others(3): Show | 6 | HG01255.hp1 HG02257.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-181_258-179del others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246660 | ||||||
chr9:36246681
|
T | G | 217 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(214): Show | 218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.258-199A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246681 | ||||||
chr9:36246681
|
T | TG | 8 | a0001c0001t0002g0107a0001c0001t0006g0224a0001c0001t0006g0225others(5): Show | 8 | HG01081.hp1 HG01167.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-200_258-199ins others(1): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246681 | ||||||
chr9:36246693
|
A | T | 3 | a0001c0001t0091g0355a0001c0001t0092g0354a0001c0001t0093g0353 | 3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.258-211T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246693 | ||||||
chr9:36246869
|
A | T | 13 | a0001c0001t0001g0252a0001c0001t0001g0284a0001c0001t0001g0298others(10): Show | 13 | HG00558.hp2 HG00609.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.258-387T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246869 | ||||||
chr9:36246947
|
G | A | 1 | a0001c0001t0084g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.258-465C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246947 | ||||||
chr9:36246965
|
G | A | 225 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(222): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.258-483C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246965 | ||||||
chr9:36246972
|
G | T | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-490C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246972 | ||||||
chr9:36247051
|
T | C | 7 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(4): Show | 7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.258-569A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247051 | ||||||
chr9:36247122
|
T | A | 1 | a0001c0001t0008g0143 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-640A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247122 | ||||||
chr9:36247201
|
C | T | 2 | a0001c0001t0039g0138a0001c0001t0039g0139 | 2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.258-719G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247201 | ||||||
chr9:36247276
|
C | A | 7 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(4): Show | 7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.258-794G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247276 | ||||||
chr9:36247298
|
G | A | 7 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(4): Show | 7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.258-816C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247298 | ||||||
chr9:36247453
|
T | C | 8 | a0001c0001t0039g0138a0001c0001t0039g0139a0001c0001t0044g0342others(5): Show | 8 | HG02280.hp1 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-971A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247453 | ||||||
chr9:36247701
|
T | A | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-1219A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247701 | ||||||
chr9:36247733
|
A | T | 2 | a0001c0002t0018g0023a0001c0002t0071g0024 | 2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.258-1251T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247733 | ||||||
chr9:36247750
|
G | A | 1 | a0001c0001t0084g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.258-1268C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247750 | ||||||
chr9:36247792
|
G | C | 232 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(229): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.258-1310C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247792 | ||||||
chr9:36247829
|
C | G | 163 | a0001c0001t0001g0081a0001c0001t0001g0114a0001c0001t0001g0158others(160): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.258-1347G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247829 | ||||||
chr9:36247983
|
G | A | 9 | a0001c0001t0001g0275a0001c0001t0039g0138a0001c0001t0039g0139others(6): Show | 9 | HG02280.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.257+1209C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247983 | ||||||
chr9:36248022
|
G | A | 4 | a0001c0001t0007g0174a0001c0001t0007g0176a0001c0001t0008g0175others(1): Show | 4 | HG01175.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+1170C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248022 | ||||||
chr9:36248026
|
C | CA | 20 | a0001c0001t0001g0241a0001c0001t0001g0246a0001c0001t0001g0267others(17): Show | 20 | HG00408.hp1 HG01192.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.257+1165dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248026 | ||||||
chr9:36248026
|
CA | C | 36 | a0001c0001t0001g0056a0001c0001t0001g0159a0001c0001t0001g0293others(33): Show | 36 | HG00280.hp1 HG01074.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.257+1165delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248026 | ||||||
chr9:36248026
|
CAA | C | 191 | a0001c0001t0001g0081a0001c0001t0001g0114a0001c0001t0001g0158others(188): Show | 192 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.257+1164_257+1165d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248026 | ||||||
chr9:36248053
|
G | A | 1 | a0001c0001t0034g0092 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.257+1139C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248053 | ||||||
chr9:36248112
|
G | A | 232 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(229): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.257+1080C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248112 | ||||||
chr9:36248295
|
T | C | 139 | a0001c0001t0001g0114a0001c0001t0001g0158a0001c0001t0001g0159others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.257+897A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248295 | ||||||
chr9:36248310
|
A | T | 3 | a0001c0002t0018g0023a0001c0002t0035g0063a0001c0002t0071g0024 | 3 | HG02647.hp2 HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.257+882T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248310 | ||||||
chr9:36248316
|
T | G | 1 | a0001c0001t0017g0078 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.257+876A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248316 | ||||||
chr9:36248318
|
C | CT | 58 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(55): Show | 59 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.257+873dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248318 | ||||||
chr9:36248337
|
G | A | 1 | a0001c0001t0100g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.257+855C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248337 | ||||||
chr9:36248443
|
T | A | 139 | a0001c0001t0001g0114a0001c0001t0001g0158a0001c0001t0001g0159others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.257+749A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248443 | ||||||
chr9:36248464
|
G | A | 7 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(4): Show | 7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.257+728C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248464 | ||||||
chr9:36248481
|
A | AT | 97 | a0001c0001t0001g0056a0001c0001t0001g0158a0001c0001t0001g0159others(94): Show | 98 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.257+710dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248481 | ||||||
chr9:36248481
|
AT | A | 13 | a0001c0001t0014g0233a0001c0001t0014g0237a0001c0001t0023g0236others(10): Show | 13 | HG02280.hp1 HG02486.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.257+710delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248481 | ||||||
chr9:36248495
|
TG | T | 3 | a0001c0001t0091g0355a0001c0001t0092g0354a0001c0001t0093g0353 | 3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.257+696delC | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248495 | ||||||
chr9:36248620
|
G | A | 2 | a0001c0001t0007g0161a0001c0001t0009g0037 | 2 | HG01943.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.257+572C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248620 | ||||||
chr9:36248694
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+498A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248694 | ||||||
chr9:36248695
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+497C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248695 | ||||||
chr9:36248697
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+495G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248697 | ||||||
chr9:36248699
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+493C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248699 | ||||||
chr9:36248700
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+492A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248700 | ||||||
chr9:36248701
|
A | G | 3 | a0001c0001t0055g0345a0001c0001t0056g0344a0001c0001t0059g0343 | 3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.257+491T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248701 | ||||||
chr9:36248703
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+489A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248703 | ||||||
chr9:36248704
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+488C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248704 | ||||||
chr9:36248705
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+487A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248705 | ||||||
chr9:36248708
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+484G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248708 | ||||||
chr9:36248709
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+483A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248709 | ||||||
chr9:36248710
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+482G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248710 | ||||||
chr9:36248711
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+481A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248711 | ||||||
chr9:36248712
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+480G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248712 | ||||||
chr9:36248713
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+479A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248713 | ||||||
chr9:36248715
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+477G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248715 | ||||||
chr9:36248716
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+476A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248716 | ||||||
chr9:36248717
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+475A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248717 | ||||||
chr9:36248718
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+474A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248718 | ||||||
chr9:36248720
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+472G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248720 | ||||||
chr9:36248721
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+471G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248721 | ||||||
chr9:36248722
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+470A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248722 | ||||||
chr9:36248724
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+468C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248724 | ||||||
chr9:36248725
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+467G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248725 | ||||||
chr9:36248727
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+465C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248727 | ||||||
chr9:36248729
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+463A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248729 | ||||||
chr9:36248730
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+462A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248730 | ||||||
chr9:36248737
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+455A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248737 | ||||||
chr9:36248738
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+454A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248738 | ||||||
chr9:36248743
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+449A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248743 | ||||||
chr9:36248744
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+448G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248744 | ||||||
chr9:36248745
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+447A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248745 | ||||||
chr9:36248746
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+446A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248746 | ||||||
chr9:36248747
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+445C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248747 | ||||||
chr9:36248748
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+444A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248748 | ||||||
chr9:36248749
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+443A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248749 | ||||||
chr9:36248750
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+442G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248750 | ||||||
chr9:36248751
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+441G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248751 | ||||||
chr9:36248753
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+439A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248753 | ||||||
chr9:36248755
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+437A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248755 | ||||||
chr9:36248756
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+436G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248756 | ||||||
chr9:36248757
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+435A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248757 | ||||||
chr9:36248759
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+433G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248759 | ||||||
chr9:36248760
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+432A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248760 | ||||||
chr9:36248762
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+430G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248762 | ||||||
chr9:36248763
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+429A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248763 | ||||||
chr9:36248765
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+427A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248765 | ||||||
chr9:36248767
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+425A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248767 | ||||||
chr9:36248770
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+422C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248770 | ||||||
chr9:36248771
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+421G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248771 | ||||||
chr9:36248772
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+420A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248772 | ||||||
chr9:36248773
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+419C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248773 | ||||||
chr9:36248774
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+418A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248774 | ||||||
chr9:36248775
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+416_257+417ins others(10): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248775 | ||||||
chr9:36248775
|
T | TGGCCTAT others(372): Show |
1 | a0001c0001t0007g0154 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.257+416_257+417ins others(379): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248775 | ||||||
chr9:36248776
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+416C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248776 | ||||||
chr9:36248777
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+415C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248777 | ||||||
chr9:36248778
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+414G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248778 | ||||||
chr9:36248779
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+413G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248779 | ||||||
chr9:36248780
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+412A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248780 | ||||||
chr9:36248782
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+410A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248782 | ||||||
chr9:36248786
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+406G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248786 | ||||||
chr9:36248787
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+405G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248787 | ||||||
chr9:36248789
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+403C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248789 | ||||||
chr9:36248790
|
T | G | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+402A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248790 | ||||||
chr9:36248791
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+401A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248791 | ||||||
chr9:36248823
|
T | A | 7 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(4): Show | 7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.257+369A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248823 | ||||||
chr9:36248828
|
A | G | 139 | a0001c0001t0001g0114a0001c0001t0001g0158a0001c0001t0001g0159others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.257+364T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248828 | ||||||
chr9:36248956
|
T | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0166 | 2 | NA18947.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.257+236A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248956 | ||||||
chr9:36248978
|
T | C | 4 | a0001c0002t0023g0026a0001c0002t0024g0025a0001c0002t0024g0028others(1): Show | 4 | HG01884.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+214A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248978 | ||||||
chr9:36249538
|
T | C | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-141A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249538 | ||||||
chr9:36249568
|
T | C | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-171A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249568 | ||||||
chr9:36249614
|
T | C | 14 | a0001c0001t0001g0081a0001c0001t0002g0076a0001c0001t0002g0079others(11): Show | 14 | HG01074.hp2 HG02622.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.52-217A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249614 | ||||||
chr9:36249626
|
C | T | 1 | a0001c0001t0005g0220 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.52-229G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249626 | ||||||
chr9:36249644
|
C | T | 5 | a0001c0001t0005g0202a0001c0001t0005g0204a0001c0001t0005g0207others(2): Show | 5 | HG00438.hp1 HG01981.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-247G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249644 | ||||||
chr9:36249645
|
G | A | 16 | a0001c0001t0001g0081a0001c0001t0002g0076a0001c0001t0002g0079others(13): Show | 16 | HG01074.hp2 HG01257.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.52-248C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249645 | ||||||
chr9:36249735
|
T | A | 1 | a0001c0001t0003g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.52-338A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249735 | ||||||
chr9:36249745
|
G | A | 16 | a0001c0001t0001g0081a0001c0001t0002g0076a0001c0001t0002g0079others(13): Show | 16 | HG01074.hp2 HG01257.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.52-348C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249745 | ||||||
chr9:36249756
|
T | A | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-359A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249756 | ||||||
chr9:36249756
|
T | C | 236 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(233): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.52-359A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249756 | ||||||
chr9:36249764
|
G | A | 1 | a0001c0001t0084g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.52-367C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249764 | ||||||
chr9:36249797
|
T | C | 7 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(4): Show | 7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-400A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249797 | ||||||
chr9:36249860
|
G | A | 6 | a0001c0001t0013g0068a0001c0001t0013g0069a0001c0001t0013g0070others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-463C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249860 | ||||||
chr9:36249980
|
G | C | 4 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0320others(1): Show | 4 | HG02109.hp1 HG02717.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-583C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249980 | ||||||
chr9:36249984
|
G | A | 4 | a0001c0002t0023g0026a0001c0002t0024g0025a0001c0002t0024g0028others(1): Show | 4 | HG01884.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-587C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249984 | ||||||
chr9:36250021
|
T | C | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-624A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250021 | ||||||
chr9:36250121
|
A | T | 225 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(222): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.52-724T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250121 | ||||||
chr9:36250158
|
G | C | 2 | a0001c0001t0039g0138a0001c0001t0039g0139 | 2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.52-761C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250158 | ||||||
chr9:36250212
|
G | T | 7 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(4): Show | 7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-815C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250212 | ||||||
chr9:36250219
|
A | G | 7 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(4): Show | 7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-822T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250219 | ||||||
chr9:36250353
|
C | T | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-956G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250353 | ||||||
chr9:36250380
|
G | C | 145 | a0001c0001t0001g0114a0001c0001t0001g0158a0001c0001t0001g0159others(142): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.52-983C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250380 | ||||||
chr9:36250593
|
A | G | 7 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(4): Show | 7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-1196T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250593 | ||||||
chr9:36250668
|
T | C | 232 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(229): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.52-1271A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250668 | ||||||
chr9:36250801
|
C | T | 8 | a0001c0002t0018g0023a0001c0002t0023g0026a0001c0002t0024g0025others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.52-1404G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250801 | ||||||
chr9:36251040
|
CTT | C | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-1645_52-1644del others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251040 | ||||||
chr9:36251288
|
C | T | 5 | a0001c0001t0014g0233a0001c0001t0014g0237a0001c0001t0023g0236others(2): Show | 5 | HG02965.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-1891G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251288 | ||||||
chr9:36251304
|
G | A | 232 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(229): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.52-1907C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251304 | ||||||
chr9:36251323
|
C | T | 8 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(5): Show | 8 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.52-1926G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251323 | ||||||
chr9:36251486
|
C | T | 4 | a0001c0002t0023g0026a0001c0002t0024g0025a0001c0002t0024g0028others(1): Show | 4 | HG01884.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-2089G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251486 | ||||||
chr9:36251529
|
C | T | 245 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(242): Show | 246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.52-2132G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251529 | ||||||
chr9:36251672
|
T | C | 5 | a0001c0002t0023g0026a0001c0002t0024g0025a0001c0002t0024g0028others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-2275A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251672 | ||||||
chr9:36251682
|
G | C | 9 | a0001c0001t0045g0010a0001c0001t0045g0018a0001c0001t0046g0014others(6): Show | 9 | HG01109.hp1 HG02622.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.52-2285C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251682 | ||||||
chr9:36251842
|
T | C | 2 | a0001c0001t0025g0217a0001c0001t0026g0213 | 2 | HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.52-2445A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251842 | ||||||
chr9:36251986
|
C | CT | 212 | a0001c0001t0001g0056a0001c0001t0001g0114a0001c0001t0001g0158others(209): Show | 213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.52-2590dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251986 | ||||||
chr9:36251986
|
C | CTT | 10 | a0001c0001t0001g0081a0001c0001t0005g0104a0001c0001t0005g0216others(7): Show | 10 | HG01257.hp2 HG01515.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.52-2591_52-2590dup others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251986 | ||||||
chr9:36251986
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0092g0354 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.52-2600_52-2590dup others(11): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251986 | ||||||
chr9:36251986
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0091g0355a0001c0001t0093g0353 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.52-2601_52-2590dup others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251986 | ||||||
chr9:36251986
|
CT | C | 11 | a0001c0001t0001g0280a0001c0001t0004g0279a0001c0001t0037g0305others(8): Show | 11 | HG01256.hp2 HG02280.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.52-2590delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251986 | ||||||
chr9:36252064
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.52-2667G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252064 | ||||||
chr9:36252134
|
T | C | 7 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(4): Show | 7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-2737A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252134 | ||||||
chr9:36252278
|
C | T | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-2881G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252278 | ||||||
chr9:36252316
|
T | C | 2 | a0001c0001t0044g0342a0001c0001t0044g0346 | 2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.52-2919A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252316 | ||||||
chr9:36252348
|
G | A | 1 | a0001c0001t0001g0281 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.52-2951C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252348 | ||||||
chr9:36252445
|
TTTGTATT others(23): Show |
T | 1 | a0001c0001t0001g0301 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.52-3078_52-3049del others(30): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252445 | ||||||
chr9:36252449
|
T | C | 2 | a0001c0001t0048g0073a0001c0001t0050g0074 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.52-3052A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252449 | ||||||
chr9:36252476
|
T | C | 1 | a0001c0001t0001g0301 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.52-3079A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252476 | ||||||
chr9:36252712
|
A | C | 245 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(242): Show | 246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.52-3315T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252712 | ||||||
chr9:36252751
|
T | G | 1 | a0001c0002t0071g0024 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.52-3354A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252751 | ||||||
chr9:36252828
|
G | GCAAA | 232 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(229): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.52-3432_52-3431ins others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252828 | ||||||
chr9:36252870
|
G | T | 1 | a0001c0002t0035g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.52-3473C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252870 | ||||||
chr9:36252925
|
G | A | 1 | a0001c0001t0005g0216 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.52-3528C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252925 | ||||||
chr9:36253043
|
TCCC | T | 7 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(4): Show | 7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-3649_52-3647del others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253043 | ||||||
chr9:36253111
|
A | G | 234 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(231): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.52-3714T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253111 | ||||||
chr9:36253208
|
T | TACATACA others(1): Show |
6 | a0001c0001t0013g0068a0001c0001t0013g0069a0001c0001t0013g0070others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-3819_52-3812dup others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253208 | ||||||
chr9:36253227
|
C | T | 2 | a0001c0001t0046g0015a0001c0001t0100g0272 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.52-3830G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253227 | ||||||
chr9:36253293
|
TA | T | 6 | a0001c0001t0002g0096a0001c0001t0009g0058a0001c0001t0015g0167others(3): Show | 6 | HG01257.hp2 HG03491.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-3897delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253293 | ||||||
chr9:36253294
|
A | T | 224 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(221): Show | 225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.52-3897T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253294 | ||||||
chr9:36253326
|
A | G | 43 | a0001c0001t0005g0104a0001c0001t0005g0189a0001c0001t0005g0198others(40): Show | 43 | HG00140.hp2 HG00438.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.52-3929T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253326 | ||||||
chr9:36253426
|
C | T | 4 | a0001c0001t0014g0237a0001c0001t0023g0236a0001c0001t0043g0234others(1): Show | 4 | HG02965.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-4029G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253426 | ||||||
chr9:36253466
|
C | T | 147 | a0001c0001t0001g0114a0001c0001t0001g0158a0001c0001t0001g0159others(144): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.52-4069G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253466 | ||||||
chr9:36253547
|
G | A | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-4150C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253547 | ||||||
chr9:36253570
|
G | A | 1 | a0001c0001t0011g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.52-4173C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253570 | ||||||
chr9:36253574
|
A | T | 2 | a0001c0002t0018g0023a0001c0002t0071g0024 | 2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.52-4177T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253574 | ||||||
chr9:36253809
|
G | A | 45 | a0001c0001t0001g0114a0001c0001t0002g0093a0001c0001t0002g0094others(42): Show | 45 | HG00280.hp2 HG00621.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.52-4412C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253809 | ||||||
chr9:36253813
|
G | A | 6 | a0001c0001t0013g0068a0001c0001t0013g0069a0001c0001t0013g0070others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-4416C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253813 | ||||||
chr9:36253829
|
C | T | 227 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(224): Show | 228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.52-4432G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253829 | ||||||
chr9:36253842
|
A | G | 1 | a0001c0001t0009g0032 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.52-4445T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253842 | ||||||
chr9:36253994
|
A | G | 234 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(231): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.52-4597T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253994 | ||||||
chr9:36254205
|
A | AAAAT | 164 | a0001c0001t0001g0081a0001c0001t0001g0114a0001c0001t0001g0158others(161): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.52-4812_52-4809dup others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254205 | ||||||
chr9:36254205
|
A | AAAATAAA others(1): Show |
53 | a0001c0001t0001g0056a0001c0001t0002g0120a0001c0001t0003g0009others(50): Show | 54 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.52-4816_52-4809dup others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254205 | ||||||
chr9:36254205
|
A | AAAATAAA others(5): Show |
11 | a0001c0001t0003g0019a0001c0001t0003g0034a0001c0001t0046g0015others(8): Show | 11 | HG01361.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.52-4820_52-4809dup others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254205 | ||||||
chr9:36254353
|
C | G | 1 | a0001c0001t0001g0056 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.52-4956G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254353 | ||||||
chr9:36254411
|
G | A | 3 | a0001c0001t0091g0355a0001c0001t0092g0354a0001c0001t0093g0353 | 3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.52-5014C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254411 | ||||||
chr9:36254473
|
A | G | 16 | a0001c0001t0001g0081a0001c0001t0002g0076a0001c0001t0002g0079others(13): Show | 16 | HG01074.hp2 HG01257.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.52-5076T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254473 | ||||||
chr9:36254513
|
C | T | 240 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(237): Show | 241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.52-5116G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254513 | ||||||
chr9:36254544
|
A | T | 147 | a0001c0001t0001g0114a0001c0001t0001g0158a0001c0001t0001g0159others(144): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.52-5147T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254544 | ||||||
chr9:36254723
|
G | A | 1 | a0001c0001t0008g0146 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.52-5326C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254723 | ||||||
chr9:36254901
|
G | A | 1 | a0001c0001t0015g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.52-5504C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254901 | ||||||
chr9:36254980
|
T | C | 245 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(242): Show | 246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.52-5583A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254980 | ||||||
chr9:36255038
|
G | T | 3 | a0001c0001t0029g0091a0001c0001t0034g0088a0001c0001t0034g0092 | 3 | HG01257.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.52-5641C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255038 | ||||||
chr9:36255230
|
C | T | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-5833G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255230 | ||||||
chr9:36255270
|
C | T | 1 | a0001c0001t0005g0008 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52-5873G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255270 | ||||||
chr9:36255341
|
G | A | 1 | a0001c0001t0001g0246 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.52-5944C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255341 | ||||||
chr9:36255386
|
T | A | 1 | a0001c0001t0004g0314 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.52-5989A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255386 | ||||||
chr9:36255434
|
T | G | 8 | a0001c0001t0011g0352a0001c0001t0038g0351a0001c0001t0040g0348others(5): Show | 8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.52-6037A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255434 | ||||||
chr9:36255575
|
C | T | 1 | a0001c0001t0003g0052 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.52-6178G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255575 | ||||||
chr9:36255672
|
T | C | 1 | a0001c0001t0013g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.52-6275A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255672 | ||||||
chr9:36255971
|
C | G | 4 | a0001c0001t0011g0352a0001c0001t0091g0355a0001c0001t0092g0354others(1): Show | 4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-6574G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255971 | ||||||
chr9:36256027
|
C | A | 165 | a0001c0001t0001g0081a0001c0001t0001g0114a0001c0001t0001g0158others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.52-6630G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256027 | ||||||
chr9:36256142
|
G | T | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | HG03491.hp1 HG03492.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.52-6745C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256142 | ||||||
chr9:36256146
|
C | T | 1 | a0001c0001t0005g0008 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52-6749G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256146 | ||||||
chr9:36256169
|
C | T | 2 | a0001c0001t0004g0265a0001c0001t0004g0266 | 2 | HG02071.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.52-6772G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256169 | ||||||
chr9:36256170
|
G | T | 2 | a0001c0001t0006g0183a0001c0001t0006g0184 | 2 | HG02080.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.52-6773C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256170 | ||||||
chr9:36256172
|
C | T | 53 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(50): Show | 54 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.52-6775G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256172 | ||||||
chr9:36256239
|
C | CT | 24 | a0001c0001t0001g0135a0001c0001t0001g0250a0001c0001t0001g0251others(21): Show | 24 | HG00438.hp2 HG00621.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.52-6843dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256239 | ||||||
chr9:36256239
|
C | CTT | 10 | a0001c0001t0001g0229a0001c0001t0004g0314a0001c0001t0021g0319others(7): Show | 10 | HG02148.hp2 HG02280.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.52-6844_52-6843dup others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256239 | ||||||
chr9:36256239
|
C | CTTTTTTT others(14): Show |
2 | a0001c0001t0048g0073a0001c0001t0050g0074 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.52-6863_52-6843dup others(21): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256239 | ||||||
chr9:36256239
|
CT | C | 30 | a0001c0001t0001g0160a0001c0001t0001g0259a0001c0001t0001g0267others(27): Show | 30 | HG00741.hp2 HG01175.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.52-6843delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256239 | ||||||
chr9:36256239
|
CTT | C | 114 | a0001c0001t0001g0114a0001c0001t0001g0159a0001c0001t0001g0163others(111): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.52-6844_52-6843del others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256239 | ||||||
chr9:36256239
|
CTTT | C | 26 | a0001c0001t0001g0081a0001c0001t0001g0158a0001c0001t0002g0076others(23): Show | 26 | HG00280.hp2 HG01069.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.52-6845_52-6843del others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256239 | ||||||
chr9:36256239
|
CTTTTTTT others(1): Show |
C | 47 | a0001c0001t0003g0009a0001c0001t0003g0019a0001c0001t0003g0022others(44): Show | 48 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.52-6850_52-6843del others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256239 | ||||||
chr9:36256258
|
TTTTTTTT others(5): Show |
T | 1 | a0001c0001t0017g0038 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.52-6873_52-6862del others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256258 | ||||||
chr9:36256264
|
TTTGAGA | T | 6 | a0001c0001t0011g0352a0001c0001t0040g0348a0001c0001t0040g0350others(3): Show | 6 | HG01255.hp1 HG02258.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-6873_52-6868del others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256264 | ||||||
chr9:36256271
|
C | G | 9 | a0001c0001t0011g0352a0001c0001t0017g0038a0001c0001t0038g0351others(6): Show | 9 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.52-6874G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256271 | ||||||
chr9:36256283
|
C | T | 4 | a0001c0001t0011g0352a0001c0001t0091g0355a0001c0001t0092g0354others(1): Show | 4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-6886G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256283 | ||||||
chr9:36256314
|
G | A | 226 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(223): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.52-6917C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256314 | ||||||
chr9:36256337
|
T | C | 245 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(242): Show | 246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.52-6940A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256337 | ||||||
chr9:36256338
|
G | A | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-6941C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256338 | ||||||
chr9:36256393
|
T | C | 234 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(231): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.52-6996A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256393 | ||||||
chr9:36256484
|
A | T | 1 | a0001c0001t0004g0314 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.52-7087T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256484 | ||||||
chr9:36256488
|
G | T | 4 | a0001c0001t0015g0150a0001c0001t0028g0145a0001c0001t0028g0179others(1): Show | 4 | HG00741.hp1 HG01255.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-7091C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256488 | ||||||
chr9:36256702
|
A | G | 1 | a0001c0001t0041g0105 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.52-7305T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256702 | ||||||
chr9:36256814
|
T | C | 234 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(231): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.52-7417A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256814 | ||||||
chr9:36256916
|
T | A | 1 | a0001c0001t0005g0206 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.52-7519A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256916 | ||||||
chr9:36256954
|
C | G | 9 | a0001c0001t0045g0010a0001c0001t0045g0018a0001c0001t0046g0014others(6): Show | 9 | HG01109.hp1 HG02622.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.52-7557G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256954 | ||||||
chr9:36256965
|
G | A | 4 | a0001c0001t0011g0352a0001c0001t0091g0355a0001c0001t0092g0354others(1): Show | 4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-7568C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256965 | ||||||
chr9:36256966
|
G | A | 4 | a0001c0001t0011g0352a0001c0001t0091g0355a0001c0001t0092g0354others(1): Show | 4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-7569C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256966 | ||||||
chr9:36256998
|
G | A | 226 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(223): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.52-7601C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256998 | ||||||
chr9:36257065
|
A | G | 10 | a0001c0001t0003g0035a0001c0001t0003g0041a0001c0001t0003g0042others(7): Show | 10 | HG00544.hp1 HG02015.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.52-7668T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257065 | ||||||
chr9:36257092
|
T | C | 1 | a0001c0001t0084g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.52-7695A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257092 | ||||||
chr9:36257154
|
A | G | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-7757T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257154 | ||||||
chr9:36257246
|
G | T | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-7849C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257246 | ||||||
chr9:36257379
|
G | C | 3 | a0001c0001t0091g0355a0001c0001t0092g0354a0001c0001t0093g0353 | 3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.52-7982C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257379 | ||||||
chr9:36257380
|
G | T | 1 | a0001c0001t0001g0229 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.52-7983C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257380 | ||||||
chr9:36257477
|
G | T | 1 | a0001c0002t0051g0341 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.52-8080C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257477 | ||||||
chr9:36257492
|
C | T | 226 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(223): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.52-8095G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257492 | ||||||
chr9:36257541
|
C | T | 4 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-8144G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257541 | ||||||
chr9:36257758
|
G | T | 9 | a0001c0001t0005g0202a0001c0001t0005g0204a0001c0001t0005g0206others(6): Show | 9 | HG00438.hp1 HG01981.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.52-8361C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257758 | ||||||
chr9:36257767
|
C | A | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-8370G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257767 | ||||||
chr9:36257800
|
C | T | 146 | a0001c0001t0001g0114a0001c0001t0001g0158a0001c0001t0001g0159others(143): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.52-8403G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257800 | ||||||
chr9:36257802
|
C | A | 6 | a0001c0001t0013g0068a0001c0001t0013g0069a0001c0001t0013g0070others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-8405G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
C | CA | 67 | a0001c0001t0001g0159a0001c0001t0001g0166a0001c0001t0001g0227others(64): Show | 68 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.52-8406dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
C | CAA | 58 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0001g0245others(55): Show | 58 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.52-8407_52-8406dup others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
C | CAAA | 50 | a0001c0001t0001g0056a0001c0001t0001g0244a0001c0001t0001g0296others(47): Show | 50 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.52-8408_52-8406dup others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
C | CAAAA | 13 | a0001c0001t0001g0257a0001c0001t0001g0304a0001c0001t0001g0310others(10): Show | 13 | HG00438.hp1 HG01074.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.52-8409_52-8406dup others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0044g0342 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.52-8415_52-8406dup others(10): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0029g0091 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.52-8416_52-8406dup others(11): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0084g0089a0001c0001t0087g0232a0001c0002t0071g0024 | 3 | HG02615.hp1 HG03225.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.52-8417_52-8406dup others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0014g0083a0001c0001t0014g0084 | 2 | HG01074.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.52-8418_52-8406dup others(13): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0018g0099a0001c0001t0046g0014 | 2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.52-8419_52-8406dup others(14): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0045g0018 | 3 | HG02622.hp1 HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.52-8420_52-8406dup others(15): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0097g0013 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52-8422_52-8406dup others(17): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0014g0087a0001c0001t0066g0180 | 2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.52-8424_52-8406dup others(19): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0095g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.52-8426_52-8406dup others(21): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
CA | C | 7 | a0001c0001t0001g0160a0001c0001t0001g0254a0001c0001t0001g0268others(4): Show | 7 | HG00738.hp1 HG01257.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-8406delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
CAAAAAAA | C | 12 | a0001c0001t0001g0114a0001c0001t0002g0121a0001c0001t0002g0122others(9): Show | 12 | HG01106.hp1 HG01109.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.52-8412_52-8406del others(7): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
CAAAAAAA others(1): Show |
C | 20 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0096others(17): Show | 20 | HG00621.hp2 HG02723.hp2 HG02896.hp1 others(17): Show |
intron_variant | MODIFIER | c.52-8413_52-8406del others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0038g0351 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.52-8416_52-8406del others(11): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0040g0348a0001c0001t0040g0350a0001c0001t0052g0347others(1): Show | 4 | HG01255.hp1 HG02486.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-8417_52-8406del others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257802
|
CAAAAAAA others(11): Show |
C | 3 | a0001c0001t0011g0208a0001c0001t0011g0209a0001c0001t0061g0219 | 3 | HG01069.hp1 HG01071.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.52-8423_52-8406del others(18): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | ||||||
chr9:36257918
|
G | T | 5 | a0001c0001t0014g0233a0001c0001t0014g0237a0001c0001t0023g0236others(2): Show | 5 | HG02965.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-8521C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257918 | ||||||
chr9:36257995
|
G | T | 226 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(223): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.52-8598C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257995 | ||||||
chr9:36258174
|
C | T | 2 | a0001c0001t0039g0138a0001c0001t0039g0139 | 2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.52-8777G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258174 | ||||||
chr9:36258270
|
G | T | 1 | a0001c0001t0011g0352 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.52-8873C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258270 | ||||||
chr9:36258273
|
G | T | 1 | a0001c0001t0009g0037 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.52-8876C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258273 | ||||||
chr9:36258297
|
C | G | 1 | a0001c0001t0041g0105 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.52-8900G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258297 | ||||||
chr9:36258550
|
C | T | 48 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.52-9153G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258550 | ||||||
chr9:36258577
|
C | G | 2 | a0001c0001t0004g0262a0001c0001t0004g0277 | 2 | HG00735.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.52-9180G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258577 | ||||||
chr9:36258633
|
T | A | 1 | a0001c0001t0046g0014 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.52-9236A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258633 | ||||||
chr9:36258780
|
G | T | 51 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(48): Show | 52 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.52-9383C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258780 | ||||||
chr9:36258798
|
T | C | 8 | a0001c0001t0011g0352a0001c0001t0038g0351a0001c0001t0040g0348others(5): Show | 8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.52-9401A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258798 | ||||||
chr9:36258849
|
C | T | 3 | a0001c0001t0091g0355a0001c0001t0092g0354a0001c0001t0093g0353 | 3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.52-9452G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258849 | ||||||
chr9:36258889
|
G | A | 1 | a0001c0001t0009g0055 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.52-9492C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258889 | ||||||
chr9:36258898
|
A | G | 1 | a0001c0002t0051g0341 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.52-9501T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258898 | ||||||
chr9:36259040
|
G | A | 6 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(3): Show | 6 | HG01884.hp1 HG02109.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-9643C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259040 | ||||||
chr9:36259057
|
G | A | 6 | a0001c0001t0013g0068a0001c0001t0013g0069a0001c0001t0013g0070others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-9660C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259057 | ||||||
chr9:36259116
|
C | A | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-9719G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259116 | ||||||
chr9:36259200
|
C | A | 1 | a0001c0001t0002g0129 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.52-9803G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259200 | ||||||
chr9:36259290
|
C | A | 234 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(231): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.52-9893G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259290 | ||||||
chr9:36259392
|
CT | C | 9 | a0001c0001t0014g0233a0001c0001t0014g0237a0001c0001t0023g0236others(6): Show | 9 | HG01255.hp1 HG02257.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.52-9996delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259392 | ||||||
chr9:36259392
|
CTT | C | 230 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(227): Show | 231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.52-9997_52-9996del others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259392 | ||||||
chr9:36259392
|
CTTT | C | 6 | a0001c0001t0013g0068a0001c0001t0013g0069a0001c0001t0013g0070others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-9998_52-9996del others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259392 | ||||||
chr9:36259585
|
C | T | 4 | a0001c0001t0011g0352a0001c0001t0091g0355a0001c0001t0092g0354others(1): Show | 4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-10188G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259585 | ||||||
chr9:36259699
|
C | T | 1 | a0001c0001t0005g0206 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.52-10302G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259699 | ||||||
chr9:36259723
|
C | T | 40 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.52-10326G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259723 | ||||||
chr9:36259799
|
T | C | 226 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(223): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.52-10402A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259799 | ||||||
chr9:36259984
|
C | T | 239 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(236): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.52-10587G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259984 | ||||||
chr9:36259997
|
G | A | 3 | a0001c0001t0003g0035a0001c0001t0082g0021a0001c0001t0086g0020 | 3 | HG02015.hp1 HG02056.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.52-10600C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259997 | ||||||
chr9:36260132
|
C | T | 2 | a0001c0001t0044g0342a0001c0001t0044g0346 | 2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.52-10735G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260132 | ||||||
chr9:36260281
|
T | TA | 49 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(46): Show | 50 | HG00408.hp2 HG01109.hp1 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.52-10885dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260281 | ||||||
chr9:36260281
|
T | TAA | 9 | a0001c0001t0078g0048a0001c0002t0018g0023a0001c0002t0023g0026others(6): Show | 9 | HG00544.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.52-10886_52-10885d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260281 | ||||||
chr9:36260281
|
TA | T | 14 | a0001c0001t0001g0159a0001c0001t0001g0238a0001c0001t0001g0245others(11): Show | 14 | HG01069.hp2 HG01167.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.52-10885delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260281 | ||||||
chr9:36260290
|
A | C | 1 | a0001c0001t0001g0338 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.52-10893T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260290 | ||||||
chr9:36260294
|
A | G | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-10897T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260294 | ||||||
chr9:36260315
|
T | A | 8 | a0001c0001t0011g0352a0001c0001t0038g0351a0001c0001t0040g0348others(5): Show | 8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.52-10918A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260315 | ||||||
chr9:36260375
|
G | T | 1 | a0001c0001t0001g0304 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.52-10978C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260375 | ||||||
chr9:36260429
|
T | C | 1 | a0001c0001t0001g0311 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.52-11032A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260429 | ||||||
chr9:36260583
|
A | G | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-11186T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260583 | ||||||
chr9:36260598
|
G | A | 2 | a0001c0001t0048g0073a0001c0001t0050g0074 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.52-11201C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260598 | ||||||
chr9:36260657
|
G | C | 8 | a0001c0001t0011g0352a0001c0001t0038g0351a0001c0001t0040g0348others(5): Show | 8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.52-11260C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260657 | ||||||
chr9:36260684
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.52-11287T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260684 | ||||||
chr9:36260721
|
T | C | 1 | a0001c0001t0046g0015 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.52-11324A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260721 | ||||||
chr9:36260725
|
C | T | 53 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(50): Show | 54 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.52-11328G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260725 | ||||||
chr9:36260762
|
G | A | 52 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(49): Show | 53 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.52-11365C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260762 | ||||||
chr9:36260786
|
G | A | 9 | a0001c0001t0045g0010a0001c0001t0045g0018a0001c0001t0046g0014others(6): Show | 9 | HG01109.hp1 HG02622.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.52-11389C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260786 | ||||||
chr9:36260868
|
C | CA | 20 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0245others(17): Show | 20 | HG00621.hp1 HG00735.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.52-11472dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260868 | ||||||
chr9:36260868
|
C | CAA | 15 | a0001c0001t0001g0244a0001c0001t0001g0250a0001c0001t0001g0267others(12): Show | 15 | HG00438.hp2 HG01109.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.52-11473_52-11472d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260868 | ||||||
chr9:36260868
|
C | CAAA | 11 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0320others(8): Show | 11 | HG00140.hp1 HG01516.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.52-11474_52-11472d others(5): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260868 | ||||||
chr9:36260868
|
C | CAAAA | 9 | a0001c0001t0001g0227a0001c0001t0001g0229a0001c0001t0001g0326others(6): Show | 9 | HG00408.hp1 HG00544.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.52-11475_52-11472d others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260868 | ||||||
chr9:36260868
|
CA | C | 17 | a0001c0001t0001g0230a0001c0001t0001g0243a0001c0001t0001g0247others(14): Show | 17 | HG00558.hp1 HG00558.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.52-11472delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260868 | ||||||
chr9:36260868
|
CAAAAA | C | 13 | a0001c0001t0005g0206a0001c0001t0005g0207a0001c0001t0005g0222others(10): Show | 13 | HG00438.hp1 HG01167.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.52-11476_52-11472d others(7): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260868 | ||||||
chr9:36260868
|
CAAAAAA | C | 101 | a0001c0001t0001g0056a0001c0001t0001g0158a0001c0001t0001g0159others(98): Show | 101 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.52-11477_52-11472d others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260868 | ||||||
chr9:36260868
|
CAAAAAAA | C | 112 | a0001c0001t0001g0081a0001c0001t0001g0114a0001c0001t0002g0079others(109): Show | 113 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.52-11478_52-11472d others(9): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260868 | ||||||
chr9:36260883
|
A | C | 2 | a0001c0001t0044g0342a0001c0001t0044g0346 | 2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.52-11486T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260883 | ||||||
chr9:36260886
|
A | C | 9 | a0001c0001t0045g0010a0001c0001t0045g0018a0001c0001t0046g0014others(6): Show | 9 | HG01109.hp1 HG02622.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.52-11489T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260886 | ||||||
chr9:36260887
|
A | C | 3 | a0001c0001t0055g0345a0001c0001t0056g0344a0001c0001t0059g0343 | 3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.52-11490T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260887 | ||||||
chr9:36260890
|
A | C | 2 | a0001c0001t0044g0342a0001c0001t0044g0346 | 2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.52-11493T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260890 | ||||||
chr9:36260893
|
A | C | 216 | a0001c0001t0001g0056a0001c0001t0001g0114a0001c0001t0001g0158others(213): Show | 217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.52-11496T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260893 | ||||||
chr9:36260894
|
A | C | 1 | a0001c0001t0007g0181 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.52-11497T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260894 | ||||||
chr9:36261114
|
A | G | 234 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(231): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.52-11717T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261114 | ||||||
chr9:36261409
|
C | T | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-12012G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261409 | ||||||
chr9:36261410
|
G | C | 1 | a0001c0001t0001g0338 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.52-12013C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261410 | ||||||
chr9:36261422
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.52-12025C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261422 | ||||||
chr9:36261426
|
G | A | 1 | a0001c0001t0008g0153 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.52-12029C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261426 | ||||||
chr9:36261463
|
G | A | 1 | a0001c0002t0049g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.52-12066C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261463 | ||||||
chr9:36261524
|
G | A | 1 | a0001c0001t0001g0333 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.52-12127C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261524 | ||||||
chr9:36261532
|
G | A | 1 | a0001c0001t0066g0180 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.52-12135C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261532 | ||||||
chr9:36261552
|
C | CA | 92 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0252others(89): Show | 93 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.52-12156dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261552 | ||||||
chr9:36261552
|
CA | C | 11 | a0001c0001t0008g0157a0001c0001t0011g0352a0001c0001t0038g0351others(8): Show | 11 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.52-12156delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261552 | ||||||
chr9:36261566
|
A | T | 1 | a0001c0001t0089g0283 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.52-12169T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261566 | ||||||
chr9:36261661
|
T | C | 1 | a0001c0001t0010g0273 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.52-12264A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261661 | ||||||
chr9:36261799
|
T | A | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-12402A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261799 | ||||||
chr9:36261800
|
G | A | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-12403C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261800 | ||||||
chr9:36261814
|
G | T | 232 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(229): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.52-12417C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261814 | ||||||
chr9:36261815
|
C | T | 233 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(230): Show | 234 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.52-12418G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261815 | ||||||
chr9:36261816
|
G | T | 1 | a0001c0001t0007g0181 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.52-12419C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261816 | ||||||
chr9:36261848
|
G | A | 61 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(58): Show | 62 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(59): Show |
intron_variant | MODIFIER | c.52-12451C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261848 | ||||||
chr9:36261922
|
CA | C | 218 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(215): Show | 219 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.52-12526delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261922 | ||||||
chr9:36261922
|
CAA | C | 12 | a0001c0001t0006g0193a0001c0001t0008g0157a0001c0001t0027g0147others(9): Show | 12 | HG01109.hp1 HG01168.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.52-12527_52-12526d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261922 | ||||||
chr9:36262086
|
A | C | 2 | a0001c0001t0014g0237a0001c0001t0094g0235 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.52-12689T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36262086 | ||||||
chr9:36262123
|
C | T | 145 | a0001c0001t0001g0056a0001c0001t0001g0114a0001c0001t0002g0093others(142): Show | 146 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.52-12726G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36262123 | ||||||
chr9:36262423
|
G | A | 1 | a0001c0001t0008g0143 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.52-13026C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36262423 | ||||||
chr9:36262629
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.52-13232C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36262629 | ||||||
chr9:36262740
|
G | A | 48 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.52-13343C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36262740 | ||||||
chr9:36263114
|
A | G | 4 | a0001c0001t0011g0352a0001c0001t0091g0355a0001c0001t0092g0354others(1): Show | 4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-13717T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263114 | ||||||
chr9:36263150
|
T | C | 1 | a0001c0001t0004g0328 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.51+13744A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263150 | ||||||
chr9:36263176
|
C | CT | 115 | a0001c0001t0001g0081a0001c0001t0001g0114a0001c0001t0001g0258others(112): Show | 115 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.51+13717dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263176 | ||||||
chr9:36263429
|
G | A | 1 | a0001c0001t0045g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.51+13465C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263429 | ||||||
chr9:36263434
|
G | A | 2 | a0001c0001t0048g0073a0001c0001t0050g0074 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.51+13460C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263434 | ||||||
chr9:36263438
|
T | G | 48 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.51+13456A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263438 | ||||||
chr9:36263445
|
A | G | 8 | a0001c0001t0011g0352a0001c0001t0038g0351a0001c0001t0040g0348others(5): Show | 8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+13449T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263445 | ||||||
chr9:36263447
|
G | A | 6 | a0001c0001t0013g0068a0001c0001t0013g0069a0001c0001t0013g0070others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+13447C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263447 | ||||||
chr9:36263456
|
C | T | 1 | a0001c0001t0011g0192 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.51+13438G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263456 | ||||||
chr9:36263528
|
T | C | 3 | a0001c0001t0055g0345a0001c0001t0056g0344a0001c0001t0059g0343 | 3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.51+13366A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263528 | ||||||
chr9:36263555
|
AC | A | 7 | a0001c0001t0044g0342a0001c0001t0044g0346a0001c0001t0052g0347others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.51+13338delG | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263555 | ||||||
chr9:36263580
|
A | G | 17 | a0001c0001t0001g0081a0001c0001t0002g0076a0001c0001t0002g0079others(14): Show | 17 | HG01074.hp2 HG01257.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.51+13314T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263580 | ||||||
chr9:36263657
|
A | G | 1 | a0001c0001t0007g0181 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+13237T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263657 | ||||||
chr9:36263658
|
G | A | 1 | a0001c0001t0007g0181 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+13236C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263658 | ||||||
chr9:36263662
|
A | T | 1 | a0001c0001t0007g0181 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+13232T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263662 | ||||||
chr9:36263672
|
T | C | 1 | a0001c0001t0080g0124 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.51+13222A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263672 | ||||||
chr9:36263803
|
G | A | 54 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(51): Show | 55 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.51+13091C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263803 | ||||||
chr9:36263903
|
G | A | 5 | a0001c0001t0014g0233a0001c0001t0014g0237a0001c0001t0023g0236others(2): Show | 5 | HG02965.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+12991C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263903 | ||||||
chr9:36263924
|
A | G | 1 | a0001c0001t0045g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.51+12970T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263924 | ||||||
chr9:36264108
|
A | G | 1 | a0001c0001t0004g0314 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.51+12786T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264108 | ||||||
chr9:36264115
|
TTTTA | T | 4 | a0001c0001t0011g0352a0001c0001t0091g0355a0001c0001t0092g0354others(1): Show | 4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+12775_51+12778d others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264115 | ||||||
chr9:36264259
|
A | G | 1 | a0001c0001t0034g0092 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.51+12635T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264259 | ||||||
chr9:36264300
|
G | T | 8 | a0001c0001t0011g0352a0001c0001t0038g0351a0001c0001t0040g0348others(5): Show | 8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+12594C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264300 | ||||||
chr9:36264449
|
A | G | 44 | a0001c0001t0005g0104a0001c0001t0005g0189a0001c0001t0005g0198others(41): Show | 44 | HG00140.hp2 HG00438.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.51+12445T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264449 | ||||||
chr9:36264545
|
C | A | 7 | a0001c0001t0011g0208a0001c0001t0011g0209a0001c0001t0011g0211others(4): Show | 7 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+12349G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264545 | ||||||
chr9:36264651
|
A | T | 1 | a0001c0001t0029g0091 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.51+12243T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264651 | ||||||
chr9:36264652
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.51+12242C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264652 | ||||||
chr9:36264677
|
G | C | 2 | a0001c0001t0001g0303a0001c0001t0001g0304 | 2 | HG01496.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.51+12217C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264677 | ||||||
chr9:36264815
|
T | C | 1 | a0001c0001t0001g0334 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.51+12079A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264815 | ||||||
chr9:36264879
|
G | A | 53 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(50): Show | 54 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.51+12015C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264879 | ||||||
chr9:36264933
|
T | C | 1 | a0001c0001t0029g0091 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.51+11961A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264933 | ||||||
chr9:36264955
|
T | C | 234 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(231): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.51+11939A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264955 | ||||||
chr9:36265008
|
G | T | 7 | a0001c0001t0044g0342a0001c0001t0044g0346a0001c0001t0052g0347others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.51+11886C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265008 | ||||||
chr9:36265031
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.51+11863C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265031 | ||||||
chr9:36265032
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.51+11862G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265032 | ||||||
chr9:36265100
|
A | G | 5 | a0001c0001t0014g0233a0001c0001t0014g0237a0001c0001t0023g0236others(2): Show | 5 | HG02965.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+11794T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265100 | ||||||
chr9:36265127
|
C | T | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | NA18944.hp2 NA18957.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.51+11767G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265127 | ||||||
chr9:36265162
|
G | A | 226 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(223): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.51+11732C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265162 | ||||||
chr9:36265356
|
A | G | 1 | a0001c0001t0035g0067 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.51+11538T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265356 | ||||||
chr9:36265469
|
C | T | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.51+11425G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265469 | ||||||
chr9:36265737
|
T | C | 246 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(243): Show | 247 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.51+11157A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265737 | ||||||
chr9:36265774
|
C | T | 4 | a0001c0001t0011g0352a0001c0001t0091g0355a0001c0001t0092g0354others(1): Show | 4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+11120G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265774 | ||||||
chr9:36265801
|
C | A | 234 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(231): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.51+11093G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265801 | ||||||
chr9:36265828
|
G | A | 8 | a0001c0001t0011g0352a0001c0001t0038g0351a0001c0001t0040g0348others(5): Show | 8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+11066C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265828 | ||||||
chr9:36265957
|
TCTCA | T | 6 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0275others(3): Show | 6 | HG02056.hp2 NA18946.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.51+10933_51+10936d others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265957 | ||||||
chr9:36265990
|
C | T | 1 | a0001c0001t0076g0103 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.51+10904G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265990 | ||||||
chr9:36266015
|
G | C | 4 | a0001c0001t0014g0237a0001c0001t0023g0236a0001c0001t0043g0234others(1): Show | 4 | HG02965.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+10879C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266015 | ||||||
chr9:36266049
|
T | A | 2 | a0001c0001t0015g0172a0001c0001t0016g0155 | 2 | HG00738.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.51+10845A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266049 | ||||||
chr9:36266087
|
G | A | 48 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.51+10807C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266087 | ||||||
chr9:36266151
|
G | A | 3 | a0001c0001t0007g0170a0001c0001t0007g0171a0001c0001t0007g0181 | 3 | NA18944.hp1 NA18955.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.51+10743C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266151 | ||||||
chr9:36266200
|
C | G | 54 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(51): Show | 55 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.51+10694G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266200 | ||||||
chr9:36266270
|
C | T | 7 | a0001c0002t0018g0023a0001c0002t0023g0026a0001c0002t0024g0025others(4): Show | 7 | HG01884.hp2 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.51+10624G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266270 | ||||||
chr9:36266287
|
G | A | 2 | a0001c0001t0015g0172a0001c0001t0016g0155 | 2 | HG00738.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.51+10607C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266287 | ||||||
chr9:36266439
|
G | A | 1 | a0001c0001t0003g0046 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.51+10455C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266439 | ||||||
chr9:36266585
|
T | A | 40 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.51+10309A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266585 | ||||||
chr9:36266591
|
C | T | 1 | a0001c0001t0013g0075 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.51+10303G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266591 | ||||||
chr9:36266826
|
G | A | 1 | a0001c0001t0026g0213 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.51+10068C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266826 | ||||||
chr9:36266886
|
A | G | 246 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(243): Show | 247 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.51+10008T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266886 | ||||||
chr9:36266891
|
T | C | 4 | a0001c0001t0011g0352a0001c0001t0091g0355a0001c0001t0092g0354others(1): Show | 4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+10003A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266891 | ||||||
chr9:36266898
|
C | CA | 7 | a0001c0001t0015g0150a0001c0001t0028g0145a0001c0001t0028g0179others(4): Show | 7 | HG00741.hp1 HG01123.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.51+9995dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266898 | ||||||
chr9:36266915
|
A | C | 1 | a0001c0001t0001g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.51+9979T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266915 | ||||||
chr9:36266937
|
C | T | 2 | a0001c0001t0082g0021a0001c0001t0086g0020 | 2 | HG02056.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.51+9957G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266937 | ||||||
chr9:36267020
|
C | T | 54 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(51): Show | 55 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.51+9874G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267020 | ||||||
chr9:36267264
|
A | G | 100 | a0001c0001t0001g0114a0001c0001t0001g0135a0001c0001t0002g0093others(97): Show | 100 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.51+9630T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267264 | ||||||
chr9:36267350
|
A | G | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.51+9544T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267350 | ||||||
chr9:36267416
|
G | A | 1 | a0001c0001t0010g0282 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.51+9478C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267416 | ||||||
chr9:36267552
|
C | T | 1 | a0001c0001t0014g0233 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.51+9342G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267552 | ||||||
chr9:36267692
|
TCAAA | T | 8 | a0001c0001t0003g0035a0001c0001t0019g0051a0001c0001t0019g0064others(5): Show | 8 | HG01255.hp1 HG01978.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+9198_51+9201del others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267692 | ||||||
chr9:36267692
|
TCAAACAA others(5): Show |
T | 7 | a0001c0002t0018g0023a0001c0002t0023g0026a0001c0002t0024g0025others(4): Show | 7 | HG01884.hp2 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.51+9190_51+9201del others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267692 | ||||||
chr9:36267748
|
A | T | 21 | a0001c0001t0001g0081a0001c0001t0002g0076a0001c0001t0002g0079others(18): Show | 21 | HG01074.hp2 HG01255.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.51+9146T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267748 | ||||||
chr9:36267828
|
G | A | 2 | a0001c0001t0020g0061a0001c0001t0020g0062 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.51+9066C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267828 | ||||||
chr9:36268008
|
G | T | 3 | a0001c0002t0018g0023a0001c0002t0035g0063a0001c0002t0071g0024 | 3 | HG02647.hp2 HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.51+8886C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268008 | ||||||
chr9:36268044
|
C | G | 246 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(243): Show | 247 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.51+8850G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268044 | ||||||
chr9:36268077
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.51+8817G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268077 | ||||||
chr9:36268220
|
C | T | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+8674G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268220 | ||||||
chr9:36268254
|
A | T | 234 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(231): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.51+8640T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268254 | ||||||
chr9:36268280
|
C | T | 98 | a0001c0001t0001g0114a0001c0001t0001g0135a0001c0001t0002g0093others(95): Show | 98 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.51+8614G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268280 | ||||||
chr9:36268387
|
T | C | 246 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(243): Show | 247 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.51+8507A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268387 | ||||||
chr9:36268410
|
A | T | 1 | a0001c0001t0007g0181 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+8484T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268410 | ||||||
chr9:36268438
|
G | A | 1 | a0001c0001t0002g0079 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.51+8456C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268438 | ||||||
chr9:36268852
|
G | T | 5 | a0001c0001t0002g0076a0001c0001t0002g0079a0001c0001t0002g0080others(2): Show | 5 | NA18967.hp2 NA18973.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+8042C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268852 | ||||||
chr9:36268950
|
C | T | 1 | a0001c0001t0003g0057 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.51+7944G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268950 | ||||||
chr9:36269045
|
G | T | 3 | a0001c0001t0010g0274a0001c0001t0010g0282a0001c0001t0010g0315 | 3 | HG00609.hp1 NA18954.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.51+7849C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269045 | ||||||
chr9:36269101
|
G | A | 1 | a0001c0001t0070g0047 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.51+7793C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269101 | ||||||
chr9:36269129
|
C | CA | 58 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.51+7764dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269129 | ||||||
chr9:36269158
|
A | G | 2 | a0001c0001t0048g0073a0001c0001t0050g0074 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.51+7736T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269158 | ||||||
chr9:36269271
|
C | T | 1 | a0001c0001t0007g0181 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+7623G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269271 | ||||||
chr9:36269320
|
G | A | 2 | a0001c0001t0048g0073a0001c0001t0050g0074 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.51+7574C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269320 | ||||||
chr9:36269415
|
T | C | 4 | a0001c0001t0007g0174a0001c0001t0007g0176a0001c0001t0008g0175others(1): Show | 4 | HG01175.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+7479A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269415 | ||||||
chr9:36269664
|
C | CT | 19 | a0001c0001t0001g0081a0001c0001t0001g0227a0001c0001t0001g0229others(16): Show | 19 | HG01074.hp2 HG01257.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.51+7229dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269664 | ||||||
chr9:36269664
|
C | CTT | 108 | a0001c0001t0001g0056a0001c0001t0001g0158a0001c0001t0001g0159others(105): Show | 109 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.51+7228_51+7229dup others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269664 | ||||||
chr9:36269664
|
C | CTTT | 19 | a0001c0001t0003g0034a0001c0001t0008g0153a0001c0001t0013g0068others(16): Show | 19 | HG01109.hp1 HG01243.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.51+7227_51+7229dup others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269664 | ||||||
chr9:36269664
|
C | CTTTT | 87 | a0001c0001t0001g0114a0001c0001t0001g0135a0001c0001t0002g0093others(84): Show | 87 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.51+7226_51+7229dup others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269664 | ||||||
chr9:36269684
|
C | T | 6 | a0001c0001t0013g0068a0001c0001t0013g0069a0001c0001t0013g0070others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+7210G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269684 | ||||||
chr9:36269700
|
C | A | 46 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.51+7194G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269700 | ||||||
chr9:36269724
|
T | C | 4 | a0001c0002t0023g0026a0001c0002t0024g0025a0001c0002t0024g0028others(1): Show | 4 | HG01884.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+7170A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269724 | ||||||
chr9:36269937
|
C | T | 8 | a0001c0001t0011g0352a0001c0001t0038g0351a0001c0001t0040g0348others(5): Show | 8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+6957G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269937 | ||||||
chr9:36269950
|
C | A | 2 | a0001c0001t0044g0342a0001c0001t0044g0346 | 2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.51+6944G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269950 | ||||||
chr9:36269958
|
G | A | 4 | a0001c0001t0011g0352a0001c0001t0091g0355a0001c0001t0092g0354others(1): Show | 4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+6936C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269958 | ||||||
chr9:36269961
|
C | T | 4 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+6933G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269961 | ||||||
chr9:36270081
|
C | G | 4 | a0001c0001t0015g0150a0001c0001t0028g0145a0001c0001t0028g0179others(1): Show | 4 | HG00741.hp1 HG01255.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+6813G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270081 | ||||||
chr9:36270172
|
A | G | 61 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(58): Show | 62 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(59): Show |
intron_variant | MODIFIER | c.51+6722T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270172 | ||||||
chr9:36270183
|
G | A | 1 | a0001c0001t0034g0092 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.51+6711C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270183 | ||||||
chr9:36270372
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.51+6522A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270372 | ||||||
chr9:36270456
|
G | A | 1 | a0001c0001t0078g0048 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.51+6438C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270456 | ||||||
chr9:36270468
|
C | T | 48 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.51+6426G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270468 | ||||||
chr9:36270516
|
C | CT | 6 | a0001c0001t0001g0267a0001c0001t0001g0281a0001c0001t0001g0308others(3): Show | 6 | HG00621.hp1 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.51+6377dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270516 | ||||||
chr9:36270516
|
CT | C | 65 | a0001c0001t0001g0056a0001c0001t0001g0245a0001c0001t0001g0246others(62): Show | 65 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.51+6377delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270516 | ||||||
chr9:36270541
|
G | A | 165 | a0001c0001t0001g0081a0001c0001t0001g0114a0001c0001t0001g0135others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.51+6353C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270541 | ||||||
chr9:36270566
|
G | A | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | NA18943.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.51+6328C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270566 | ||||||
chr9:36270566
|
G | C | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+6328C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270566 | ||||||
chr9:36270567
|
T | G | 246 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(243): Show | 247 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.51+6327A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270567 | ||||||
chr9:36270579
|
A | G | 241 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(238): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.51+6315T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270579 | ||||||
chr9:36270603
|
C | T | 9 | a0001c0001t0045g0010a0001c0001t0045g0018a0001c0001t0046g0014others(6): Show | 9 | HG01109.hp1 HG02622.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.51+6291G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270603 | ||||||
chr9:36270604
|
G | A | 1 | a0001c0001t0007g0178 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.51+6290C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270604 | ||||||
chr9:36270619
|
A | G | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.51+6275T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270619 | ||||||
chr9:36270630
|
A | G | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.51+6264T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270630 | ||||||
chr9:36270672
|
C | T | 8 | a0001c0001t0011g0352a0001c0001t0038g0351a0001c0001t0040g0348others(5): Show | 8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+6222G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270672 | ||||||
chr9:36270675
|
G | A | 5 | a0001c0001t0036g0126a0001c0001t0036g0127a0001c0001t0055g0345others(2): Show | 5 | HG03195.hp1 HG06807.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+6219C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270675 | ||||||
chr9:36270679
|
G | A | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+6215C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270679 | ||||||
chr9:36270708
|
G | A | 6 | a0001c0001t0013g0068a0001c0001t0013g0069a0001c0001t0013g0070others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+6186C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270708 | ||||||
chr9:36270883
|
C | T | 165 | a0001c0001t0001g0081a0001c0001t0001g0114a0001c0001t0001g0135others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.51+6011G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270883 | ||||||
chr9:36270991
|
T | A | 1 | a0001c0001t0007g0181 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+5903A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270991 | ||||||
chr9:36271036
|
A | T | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+5858T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36271036 | ||||||
chr9:36271130
|
G | A | 2 | a0001c0001t0048g0073a0001c0001t0050g0074 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.51+5764C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36271130 | ||||||
chr9:36271405
|
G | A | 8 | a0001c0001t0011g0352a0001c0001t0038g0351a0001c0001t0040g0348others(5): Show | 8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+5489C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36271405 | ||||||
chr9:36271481
|
C | T | 1 | a0001c0001t0007g0181 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+5413G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36271481 | ||||||
chr9:36271482
|
T | C | 1 | a0001c0001t0007g0181 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+5412A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36271482 | ||||||
chr9:36271483
|
C | T | 1 | a0001c0001t0007g0181 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+5411G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36271483 | ||||||
chr9:36271505
|
C | T | 2 | a0001c0001t0044g0342a0001c0001t0044g0346 | 2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.51+5389G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36271505 | ||||||
chr9:36271997
|
A | G | 1 | a0001c0001t0011g0352 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.51+4897T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36271997 | ||||||
chr9:36272067
|
C | G | 1 | a0001c0001t0004g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4827G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272067 | ||||||
chr9:36272100
|
A | T | 1 | a0001c0001t0004g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4794T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272100 | ||||||
chr9:36272103
|
C | G | 1 | a0001c0001t0004g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4791G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272103 | ||||||
chr9:36272126
|
A | T | 1 | a0001c0001t0004g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4768T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272126 | ||||||
chr9:36272129
|
A | T | 1 | a0001c0001t0004g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4765T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272129 | ||||||
chr9:36272130
|
C | G | 1 | a0001c0001t0004g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4764G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272130 | ||||||
chr9:36272131
|
A | C | 1 | a0001c0001t0004g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4763T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272131 | ||||||
chr9:36272138
|
G | A | 1 | a0001c0001t0004g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4756C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272138 | ||||||
chr9:36272140
|
A | G | 1 | a0001c0001t0004g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4754T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272140 | ||||||
chr9:36272147
|
C | A | 1 | a0001c0001t0004g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4747G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272147 | ||||||
chr9:36272202
|
A | G | 1 | a0001c0001t0004g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4692T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272202 | ||||||
chr9:36272203
|
T | G | 1 | a0001c0001t0004g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4691A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272203 | ||||||
chr9:36272233
|
G | C | 1 | a0001c0001t0004g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4661C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272233 | ||||||
chr9:36272234
|
C | A | 1 | a0001c0001t0004g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4660G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272234 | ||||||
chr9:36272235
|
A | T | 1 | a0001c0001t0004g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4659T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272235 | ||||||
chr9:36272252
|
A | T | 1 | a0001c0001t0004g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4642T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272252 | ||||||
chr9:36272253
|
G | A | 1 | a0001c0001t0004g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4641C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272253 | ||||||
chr9:36272264
|
C | A | 2 | a0001c0001t0044g0342a0001c0001t0044g0346 | 2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.51+4630G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272264 | ||||||
chr9:36272479
|
G | A | 1 | a0001c0001t0031g0128 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.51+4415C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272479 | ||||||
chr9:36272492
|
G | A | 17 | a0001c0001t0001g0081a0001c0001t0002g0076a0001c0001t0002g0079others(14): Show | 17 | HG01074.hp2 HG01257.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.51+4402C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272492 | ||||||
chr9:36272620
|
C | CA | 24 | a0001c0001t0001g0228a0001c0001t0001g0241a0001c0001t0001g0242others(21): Show | 24 | HG00438.hp2 HG00621.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.51+4273dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272620 | ||||||
chr9:36272620
|
C | CAA | 7 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(4): Show | 7 | HG03491.hp1 HG03492.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+4272_51+4273dup others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272620 | ||||||
chr9:36272620
|
CA | C | 20 | a0001c0001t0001g0280a0001c0001t0001g0322a0001c0001t0004g0249others(17): Show | 20 | HG00609.hp2 HG01891.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.51+4273delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272620 | ||||||
chr9:36272620
|
CAA | C | 13 | a0001c0001t0002g0076a0001c0001t0002g0080a0001c0001t0003g0057others(10): Show | 13 | HG01346.hp2 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.51+4272_51+4273del others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272620 | ||||||
chr9:36272620
|
CAAA | C | 128 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0158others(125): Show | 129 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.51+4271_51+4273del others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272620 | ||||||
chr9:36272620
|
CAAAA | C | 95 | a0001c0001t0001g0114a0001c0001t0001g0135a0001c0001t0002g0093others(92): Show | 95 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.51+4270_51+4273del others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272620 | ||||||
chr9:36272685
|
G | A | 1 | a0001c0001t0034g0088 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.51+4209C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272685 | ||||||
chr9:36272801
|
T | A | 2 | a0001c0001t0003g0059a0001c0001t0003g0060 | 2 | NA19064.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.51+4093A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272801 | ||||||
chr9:36272914
|
AT | A | 4 | a0001c0001t0006g0183a0001c0001t0006g0185a0001c0001t0084g0089others(1): Show | 4 | HG03225.hp1 NA18946.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+3979delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272914 | ||||||
chr9:36272915
|
T | A | 5 | a0001c0001t0005g0189a0001c0001t0006g0184a0001c0001t0006g0187others(2): Show | 5 | HG02080.hp1 NA18953.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+3979A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272915 | ||||||
chr9:36272916
|
AC | A | 135 | a0001c0001t0001g0081a0001c0001t0001g0114a0001c0001t0001g0158others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.51+3977delG | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272916 | ||||||
chr9:36272917
|
C | A | 28 | a0001c0001t0001g0135a0001c0001t0002g0096a0001c0001t0002g0098others(25): Show | 28 | HG00735.hp1 HG01168.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.51+3977G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272917 | ||||||
chr9:36272917
|
C | CA | 27 | a0001c0001t0001g0228a0001c0001t0001g0257a0001c0001t0001g0258others(24): Show | 27 | HG00408.hp1 HG00438.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.51+3976dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272917 | ||||||
chr9:36272917
|
CA | C | 49 | a0001c0001t0003g0009a0001c0001t0003g0019a0001c0001t0003g0022others(46): Show | 50 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.51+3976delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272917 | ||||||
chr9:36272924
|
A | T | 1 | a0001c0001t0090g0149 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.51+3970T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272924 | ||||||
chr9:36272925
|
A | T | 1 | a0001c0001t0008g0143 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.51+3969T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272925 | ||||||
chr9:36272926
|
A | T | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | NA19002.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.51+3968T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272926 | ||||||
chr9:36272964
|
A | G | 1 | a0001c0001t0060g0191 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.51+3930T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272964 | ||||||
chr9:36272971
|
G | A | 3 | a0001c0001t0003g0059a0001c0001t0003g0060a0001c0001t0074g0030 | 3 | NA18956.hp1 NA19064.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.51+3923C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272971 | ||||||
chr9:36273041
|
C | T | 1 | a0001c0001t0097g0013 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.51+3853G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273041 | ||||||
chr9:36273064
|
G | A | 234 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(231): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.51+3830C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273064 | ||||||
chr9:36273110
|
T | C | 3 | a0001c0002t0018g0023a0001c0002t0035g0063a0001c0002t0071g0024 | 3 | HG02647.hp2 HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.51+3784A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273110 | ||||||
chr9:36273112
|
G | T | 1 | a0001c0001t0002g0137 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.51+3782C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273112 | ||||||
chr9:36273119
|
T | C | 1 | a0001c0001t0066g0180 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.51+3775A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273119 | ||||||
chr9:36273178
|
C | T | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | NA18944.hp2 NA18957.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.51+3716G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273178 | ||||||
chr9:36273221
|
A | AT | 70 | a0001c0001t0001g0081a0001c0001t0001g0158a0001c0001t0001g0159others(67): Show | 70 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.51+3672dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273221 | ||||||
chr9:36273221
|
A | ATT | 15 | a0001c0001t0002g0137a0001c0001t0007g0142a0001c0001t0013g0068others(12): Show | 15 | HG01099.hp1 HG01168.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.51+3671_51+3672dup others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273221 | ||||||
chr9:36273221
|
A | ATTT | 86 | a0001c0001t0001g0114a0001c0001t0001g0135a0001c0001t0002g0093others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.51+3670_51+3672dup others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273221 | ||||||
chr9:36273221
|
A | T | 2 | a0001c0001t0014g0237a0001c0001t0094g0235 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.51+3673T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273221 | ||||||
chr9:36273221
|
AT | A | 7 | a0001c0001t0003g0029a0001c0001t0020g0061a0001c0001t0020g0062others(4): Show | 7 | HG01515.hp2 HG01517.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+3672delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273221 | ||||||
chr9:36273577
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.51+3317T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273577 | ||||||
chr9:36273660
|
CT | C | 123 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0158others(120): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.51+3233delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273660 | ||||||
chr9:36273701
|
A | G | 1 | a0001c0001t0007g0181 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+3193T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273701 | ||||||
chr9:36273702
|
G | A | 1 | a0001c0001t0007g0181 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+3192C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273702 | ||||||
chr9:36273763
|
C | G | 3 | a0001c0001t0055g0345a0001c0001t0056g0344a0001c0001t0059g0343 | 3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.51+3131G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273763 | ||||||
chr9:36273820
|
G | T | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.51+3074C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273820 | ||||||
chr9:36273831
|
G | A | 226 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(223): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.51+3063C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273831 | ||||||
chr9:36273841
|
C | T | 1 | a0001c0001t0032g0001 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.51+3053G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273841 | ||||||
chr9:36273917
|
G | A | 54 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(51): Show | 55 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.51+2977C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273917 | ||||||
chr9:36273925
|
G | A | 1 | a0001c0001t0041g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.51+2969C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273925 | ||||||
chr9:36274068
|
C | CTG | 6 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(3): Show | 6 | HG02280.hp1 HG02683.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+2824_51+2825dup others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | ||||||
chr9:36274068
|
C | CTGTGTG | 4 | a0001c0001t0002g0076a0001c0001t0023g0236a0001c0001t0038g0351others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2820_51+2825dup others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | ||||||
chr9:36274068
|
C | CTGTGTGT others(1): Show |
3 | a0001c0001t0040g0350a0001c0001t0085g0349a0001c0001t0094g0235 | 3 | HG01255.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.51+2818_51+2825dup others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | ||||||
chr9:36274068
|
C | CTGTGTGT others(3): Show |
2 | a0001c0001t0014g0233a0001c0001t0043g0234 | 2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.51+2816_51+2825dup others(10): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | ||||||
chr9:36274068
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0040g0348 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.51+2814_51+2825dup others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | ||||||
chr9:36274068
|
CTG | C | 7 | a0001c0001t0001g0081a0001c0001t0001g0242a0001c0001t0001g0243others(4): Show | 7 | HG02735.hp2 HG03195.hp1 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+2824_51+2825del others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | ||||||
chr9:36274068
|
CTGTG | C | 24 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(21): Show | 24 | HG00609.hp2 HG01074.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.51+2822_51+2825del others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | ||||||
chr9:36274068
|
CTGTGTG | C | 20 | a0001c0001t0001g0261a0001c0001t0001g0267a0001c0001t0001g0268others(17): Show | 20 | HG00609.hp1 HG00735.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.51+2820_51+2825del others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | ||||||
chr9:36274068
|
CTGTGTGT others(1): Show |
C | 46 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0281others(43): Show | 46 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.51+2818_51+2825del others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | ||||||
chr9:36274068
|
CTGTGTGT others(3): Show |
C | 26 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(23): Show | 26 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.51+2816_51+2825del others(10): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | ||||||
chr9:36274068
|
CTGTGTGT others(5): Show |
C | 19 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0335others(16): Show | 19 | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.51+2814_51+2825del others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | ||||||
chr9:36274068
|
CTGTGTGT others(7): Show |
C | 101 | a0001c0001t0001g0056a0001c0001t0001g0114a0001c0001t0001g0135others(98): Show | 102 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.51+2812_51+2825del others(14): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | ||||||
chr9:36274068
|
CTGTGTGT others(9): Show |
C | 83 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.51+2810_51+2825del others(16): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | ||||||
chr9:36274068
|
CTGTGTGT others(11): Show |
C | 5 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0007g0181others(2): Show | 5 | HG01081.hp1 HG01243.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+2808_51+2825del others(18): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | ||||||
chr9:36274068
|
CTGTGTGT others(13): Show |
C | 1 | a0001c0001t0044g0346 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.51+2806_51+2825del others(20): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | ||||||
chr9:36274115
|
T | A | 7 | a0001c0001t0001g0339a0001c0001t0012g0002a0001c0001t0012g0003others(4): Show | 7 | HG02056.hp2 HG02451.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+2779A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274115 | ||||||
chr9:36274363
|
T | C | 48 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.51+2531A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274363 | ||||||
chr9:36274465
|
A | G | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2429T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274465 | ||||||
chr9:36274846
|
C | CCG | 227 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(224): Show | 228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.51+2046_51+2047dup others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274846 | ||||||
chr9:36274868
|
A | G | 90 | a0001c0001t0001g0114a0001c0001t0001g0135a0001c0001t0002g0093others(87): Show | 90 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.51+2026T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274868 | ||||||
chr9:36274876
|
T | C | 1 | a0001c0001t0013g0075 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.51+2018A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274876 | ||||||
chr9:36274879
|
T | C | 1 | a0001c0001t0013g0075 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.51+2015A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274879 | ||||||
chr9:36274885
|
G | T | 1 | a0001c0001t0011g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.51+2009C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274885 | ||||||
chr9:36274959
|
C | T | 1 | a0001c0001t0087g0232 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.51+1935G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274959 | ||||||
chr9:36274970
|
G | A | 1 | a0001c0001t0004g0340 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.51+1924C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274970 | ||||||
chr9:36274974
|
T | C | 1 | a0001c0001t0052g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.51+1920A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274974 | ||||||
chr9:36275046
|
A | T | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+1848T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275046 | ||||||
chr9:36275065
|
T | C | 17 | a0001c0001t0001g0081a0001c0001t0002g0076a0001c0001t0002g0079others(14): Show | 17 | HG01074.hp2 HG01257.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.51+1829A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275065 | ||||||
chr9:36275204
|
C | T | 1 | a0001c0001t0003g0019 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.51+1690G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275204 | ||||||
chr9:36275403
|
G | T | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | HG03491.hp1 HG03492.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.51+1491C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275403 | ||||||
chr9:36275448
|
G | C | 17 | a0001c0001t0001g0081a0001c0001t0002g0076a0001c0001t0002g0079others(14): Show | 17 | HG01074.hp2 HG01257.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.51+1446C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275448 | ||||||
chr9:36275564
|
G | T | 4 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0095others(1): Show | 4 | NA18945.hp2 NA18957.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+1330C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275564 | ||||||
chr9:36275702
|
C | G | 9 | a0001c0001t0045g0010a0001c0001t0045g0018a0001c0001t0046g0014others(6): Show | 9 | HG01109.hp1 HG02622.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.51+1192G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275702 | ||||||
chr9:36275724
|
A | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.51+1170T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275724 | ||||||
chr9:36275851
|
T | C | 7 | a0001c0001t0044g0342a0001c0001t0044g0346a0001c0001t0052g0347others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.51+1043A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275851 | ||||||
chr9:36275894
|
A | G | 1 | a0001c0001t0007g0140 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.51+1000T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275894 | ||||||
chr9:36275895
|
G | A | 1 | a0001c0001t0006g0066 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.51+999C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275895 | ||||||
chr9:36275910
|
C | A | 1 | a0001c0001t0035g0067 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.51+984G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275910 | ||||||
chr9:36275920
|
C | T | 1 | a0001c0001t0003g0009 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.51+974G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275920 | ||||||
chr9:36275930
|
T | C | 92 | a0001c0001t0001g0114a0001c0001t0001g0135a0001c0001t0002g0093others(89): Show | 92 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.51+964A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275930 | ||||||
chr9:36276027
|
G | A | 48 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.51+867C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276027 | ||||||
chr9:36276059
|
A | G | 234 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(231): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.51+835T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276059 | ||||||
chr9:36276175
|
AACAC | A | 44 | a0001c0001t0002g0218a0001c0001t0005g0189a0001c0001t0005g0198others(41): Show | 44 | HG00140.hp2 HG00438.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.51+715_51+718delGT others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276175 | ||||||
chr9:36276186
|
A | G | 61 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0003g0019others(58): Show | 62 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(59): Show |
intron_variant | MODIFIER | c.51+708T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276186 | ||||||
chr9:36276282
|
A | G | 4 | a0001c0001t0038g0351a0001c0001t0040g0348a0001c0001t0040g0350others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+612T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276282 | ||||||
chr9:36276546
|
T | A | 234 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(231): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.51+348A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276546 | ||||||
chr9:36276600
|
A | G | 1 | a0001c0001t0005g0008 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.51+294T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276600 | ||||||
chr9:36276831
|
T | C | 1 | a0001c0001t0031g0226 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.51+63A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276831 | ||||||
chr9:36276860
|
A | G | 226 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0114others(223): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.51+34T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276860 |