geneid | 23295 |
---|---|
ensemblid | ENSG00000102858.13 |
hgncid | 20254 |
symbol | MGRN1 |
name | mahogunin ring finger 1 |
refseq_nuc | NM_015246.4 |
refseq_prot | NP_056061.1 |
ensembl_nuc | ENST00000262370.12 |
ensembl_prot | ENSP00000262370.6 |
mane_status | MANE Select |
chr | chr16 |
start | 4624826 |
end | 4690972 |
strand | + |
ver | v1.2 |
region | chr16:4624826-4690972 |
region5000 | chr16:4619826-4695972 |
regionname0 | MGRN1_chr16_4624826_4690972 |
regionname5000 | MGRN1_chr16_4619826_4695972 |
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 | 576 | 331 | 88 | 56 | 130 | 16 | 39 | 90 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0002 | 0/0 | 168 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0003 | 0/0 | 576 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0004 | 0/0 | 576 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
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 | 1/0 | 1731 | 321 | 82 | 53 | 130 | 16 | 39 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
c0002 | 0/0 | 1731 | 4 | 3 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
c0003 | 0/0 | 1731 | 3 | 1 | 2 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
c0004 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
c0005 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
c0006 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
c0007 | 0/0 | 1731 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
c0008 | 0/1 | 1731 | 1 | 0 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
c0009 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2199 | 86 | 5 | 22 | 43 | 6 | 10 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0002 | 0/0 | 2200 | 66 | 8 | 13 | 35 | 1 | 9 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0003 | 1/0 | 2200 | 32 | 14 | 2 | 10 | 2 | 3 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0004 | 0/0 | 2199 | 15 | 4 | 4 | 6 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0005 | 0/0 | 2199 | 14 | 14 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0006 | 0/0 | 2200 | 14 | 2 | 2 | 6 | 2 | 2 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0007 | 0/0 | 2200 | 10 | 1 | 3 | 6 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0008 | 0/0 | 2200 | 8 | 8 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0009 | 0/0 | 2200 | 8 | 8 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0010 | 0/0 | 2199 | 6 | 0 | 0 | 6 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0011 | 0/0 | 2199 | 6 | 1 | 1 | 3 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0012 | 0/0 | 2198 | 5 | 0 | 2 | 2 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0013 | 0/0 | 2200 | 5 | 0 | 0 | 0 | 1 | 4 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0014 | 0/0 | 2200 | 4 | 3 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0015 | 0/0 | 2199 | 4 | 0 | 1 | 0 | 0 | 3 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0016 | 0/0 | 2200 | 2 | 0 | 0 | 0 | 1 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0017 | 0/0 | 2199 | 2 | 0 | 0 | 2 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0018 | 0/0 | 2200 | 2 | 0 | 2 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0019 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0020 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0021 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0022 | 0/0 | 2200 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0023 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0024 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0025 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0026 | 0/0 | 2198 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0027 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0028 | 0/0 | 2199 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0029 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0030 | 0/0 | 2200 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0031 | 0/0 | 2200 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0032 | 0/0 | 2200 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0033 | 0/0 | 2200 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0034 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0035 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0036 | 0/0 | 2200 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0037 | 0/0 | 2200 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0038 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0039 | 0/0 | 2200 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0040 | 0/0 | 2198 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0041 | 0/0 | 2198 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0042 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0043 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0044 | 0/0 | 2199 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0045 | 0/0 | 2199 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0046 | 0/0 | 2199 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0047 | 0/0 | 2199 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0048 | 0/0 | 2198 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0049 | 0/0 | 2199 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0050 | 0/0 | 2200 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0051 | 0/0 | 2200 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0052 | 0/0 | 2200 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0053 | 0/0 | 2200 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0054 | 0/1 | 2200 | 1 | 0 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0055 | 0/0 | 2200 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0056 | 0/0 | 2200 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0057 | 0/0 | 2200 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0058 | 0/0 | 2200 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0059 | 0/0 | 2200 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0060 | 0/0 | 2200 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0061 | 0/0 | 2200 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0062 | 0/0 | 2200 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
t0063 | 0/0 | 2200 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
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 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0016 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0187 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
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 | 1/0 | 1731 | 321 | 82 | 53 | 130 | 16 | 39 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0002 | 0/0 | 1731 | 4 | 3 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0003 | 0/0 | 1731 | 3 | 1 | 2 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0004 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0006 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0008 | 0/1 | 1731 | 1 | 0 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0002c0009 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0003c0007 | 0/0 | 1731 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0004c0005 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3929 | 83 | 5 | 22 | 41 | 6 | 9 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0002 | 0/0 | 3930 | 66 | 8 | 13 | 35 | 1 | 9 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0003 | 1/0 | 3930 | 30 | 13 | 1 | 10 | 2 | 3 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0004 | 0/0 | 3929 | 14 | 3 | 4 | 6 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0005 | 0/0 | 3929 | 13 | 13 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0006 | 0/0 | 3930 | 14 | 2 | 2 | 6 | 2 | 2 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0007 | 0/0 | 3930 | 10 | 1 | 3 | 6 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0008 | 0/0 | 3930 | 8 | 8 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0009 | 0/0 | 3930 | 7 | 7 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0010 | 0/0 | 3929 | 6 | 0 | 0 | 6 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0011 | 0/0 | 3929 | 6 | 1 | 1 | 3 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0012 | 0/0 | 3928 | 5 | 0 | 2 | 2 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0013 | 0/0 | 3930 | 5 | 0 | 0 | 0 | 1 | 4 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0014 | 0/0 | 3930 | 4 | 3 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0015 | 0/0 | 3929 | 4 | 0 | 1 | 0 | 0 | 3 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0016 | 0/0 | 3930 | 2 | 0 | 0 | 0 | 1 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0017 | 0/0 | 3929 | 2 | 0 | 0 | 2 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0019 | 0/0 | 3929 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0020 | 0/0 | 3929 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0021 | 0/0 | 3929 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0022 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0023 | 0/0 | 3929 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0024 | 0/0 | 3929 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0025 | 0/0 | 3929 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0026 | 0/0 | 3928 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0027 | 0/0 | 3929 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0028 | 0/0 | 3929 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0029 | 0/0 | 3929 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0030 | 0/0 | 3930 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0031 | 0/0 | 3930 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0032 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0033 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0034 | 0/0 | 3929 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0035 | 0/0 | 3929 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0037 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0039 | 0/0 | 3930 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0040 | 0/0 | 3928 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0041 | 0/0 | 3928 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0042 | 0/0 | 3929 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0043 | 0/0 | 3929 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0044 | 0/0 | 3929 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0045 | 0/0 | 3929 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0046 | 0/0 | 3929 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0047 | 0/0 | 3929 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0048 | 0/0 | 3928 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0049 | 0/0 | 3929 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0050 | 0/0 | 3930 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0051 | 0/0 | 3930 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0052 | 0/0 | 3930 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0053 | 0/0 | 3930 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0055 | 0/0 | 3930 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0056 | 0/0 | 3930 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0057 | 0/0 | 3930 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0058 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0059 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0060 | 0/0 | 3930 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0061 | 0/0 | 3930 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0062 | 0/0 | 3930 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0001t0063 | 0/0 | 3930 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0002t0003 | 0/0 | 3930 | 2 | 1 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0002t0004 | 0/0 | 3929 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0002t0005 | 0/0 | 3929 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0003t0018 | 0/0 | 3930 | 2 | 0 | 2 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0003t0038 | 0/0 | 3929 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0004t0036 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0006t0009 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0001c0008t0054 | 0/1 | 3930 | 1 | 0 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0002c0009t0001 | 0/0 | 3929 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0003c0007t0001 | 0/0 | 3929 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
a0004c0005t0001 | 0/0 | 3929 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | copy fasta | chr16 | 4619826 | 4695972 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0016 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0006g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0006g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0006g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0006g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0007g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0007g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0007g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0007g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0007g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0007g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0007g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0007g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0007g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0009g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0009g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0009g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0009g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0009g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0009g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0010g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0010g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0010g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0010g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0010g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0010g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0011g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0011g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0011g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0011g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0011g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0011g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0012g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0012g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0012g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0012g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0012g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0013g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0013g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0013g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0013g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0013g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0014g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0014g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0014g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0014g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0015g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0015g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0015g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0015g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0016g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0016g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0017g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0017g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0019g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0020g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0021g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0022g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0023g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0024g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0025g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0026g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0027g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0028g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0029g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0030g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0031g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0032g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0033g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0034g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0035g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0037g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0039g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0040g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0041g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0042g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0043g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0044g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0045g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0046g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0047g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0048g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0049g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0050g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0051g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0052g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0053g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0055g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0056g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0057g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0058g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0059g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0060g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0061g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0062g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0001t0063g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0002t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0002t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0002t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0002t0005g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0003t0018g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0003t0018g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0003t0038g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0004t0036g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0006t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0001c0008t0054g0187 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0002c0009t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0003c0007t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
a0004c0005t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0067 | EUR | GBR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | GBR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00140 | hp2 | a0001 | c0001 | t0031 | g0046 | EUR | GBR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00280 | hp1 | a0001 | c0001 | t0006 | g0164 | EUR | FIN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00323 | hp1 | a0001 | c0001 | t0006 | g0157 | EUR | FIN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00323 | hp2 | a0001 | c0001 | t0048 | g0177 | EUR | FIN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00408 | hp1 | a0001 | c0001 | t0047 | g0283 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00423 | hp2 | a0001 | c0001 | t0017 | g0176 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00597 | hp1 | a0001 | c0001 | t0007 | g0303 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0069 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00673 | hp1 | a0001 | c0001 | t0007 | g0254 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00738 | hp2 | a0001 | c0001 | t0015 | g0203 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00741 | hp1 | a0001 | c0001 | t0060 | g0238 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG00741 | hp2 | a0001 | c0001 | t0007 | g0159 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01074 | hp1 | a0001 | c0001 | t0007 | g0167 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01081 | hp1 | a0001 | c0001 | t0051 | g0209 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01099 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0068 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0050 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01167 | hp1 | a0001 | c0003 | t0018 | g0109 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01169 | hp1 | a0001 | c0003 | t0018 | g0110 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0257 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01257 | hp1 | a0001 | c0001 | t0012 | g0195 | AMR | CLM | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | CLM | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01361 | hp1 | a0001 | c0001 | t0007 | g0302 | AMR | CLM | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0073 | EUR | IBS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01515 | hp2 | a0001 | c0001 | t0013 | g0194 | EUR | IBS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0193 | EUR | IBS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0072 | EUR | IBS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01884 | hp1 | a0001 | c0001 | t0032 | g0002 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01891 | hp1 | a0001 | c0001 | t0058 | g0329 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0041 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01975 | hp1 | a0001 | c0001 | t0012 | g0180 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02055 | hp1 | a0001 | c0006 | t0009 | g0099 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02056 | hp1 | a0001 | c0001 | t0006 | g0252 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02071 | hp1 | a0001 | c0001 | t0055 | g0278 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02129 | hp1 | a0001 | c0001 | t0006 | g0199 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02148 | hp1 | a0001 | c0001 | t0006 | g0132 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02148 | hp2 | a0001 | c0001 | t0011 | g0275 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02155 | hp2 | a0001 | c0001 | t0007 | g0292 | EAS | CDX | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02165 | hp1 | a0001 | c0001 | t0007 | g0312 | EAS | CDX | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CDX | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02257 | hp1 | a0001 | c0001 | t0059 | g0135 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02257 | hp2 | a0001 | c0001 | t0014 | g0096 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0100 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02273 | hp1 | a0001 | c0001 | t0053 | g0322 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0086 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0219 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02572 | hp1 | a0001 | c0001 | t0009 | g0090 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02602 | hp1 | a0001 | c0001 | t0006 | g0227 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02602 | hp2 | a0001 | c0001 | t0015 | g0116 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02615 | hp1 | a0001 | c0001 | t0008 | g0095 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02615 | hp2 | a0001 | c0001 | t0033 | g0021 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02622 | hp1 | a0001 | c0001 | t0011 | g0152 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02622 | hp2 | a0001 | c0001 | t0019 | g0010 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02630 | hp2 | a0001 | c0001 | t0043 | g0190 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0077 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02723 | hp2 | a0001 | c0001 | t0022 | g0014 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02735 | hp2 | a0001 | c0001 | t0011 | g0290 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02809 | hp2 | a0001 | c0004 | t0036 | g0087 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02886 | hp1 | a0001 | c0001 | t0024 | g0085 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02886 | hp2 | a0001 | c0001 | t0014 | g0019 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02896 | hp1 | a0001 | c0001 | t0035 | g0333 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02896 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02922 | hp1 | a0001 | c0001 | t0023 | g0006 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0037 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0036 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02970 | hp2 | a0001 | c0001 | t0014 | g0020 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03098 | hp1 | a0001 | c0001 | t0021 | g0042 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03130 | hp2 | a0001 | c0001 | t0020 | g0012 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03139 | hp1 | a0001 | c0002 | t0005 | g0001 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0154 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03195 | hp1 | a0001 | c0002 | t0004 | g0003 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03195 | hp2 | a0001 | c0003 | t0038 | g0018 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03209 | hp1 | a0001 | c0001 | t0009 | g0076 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03225 | hp1 | a0001 | c0001 | t0042 | g0189 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03225 | hp2 | a0001 | c0001 | t0009 | g0092 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0304 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0084 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03453 | hp2 | a0001 | c0001 | t0009 | g0075 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03490 | hp1 | a0001 | c0001 | t0012 | g0192 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03490 | hp2 | a0001 | c0001 | t0061 | g0294 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03516 | hp1 | a0001 | c0001 | t0008 | g0024 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0035 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03540 | hp2 | a0001 | c0001 | t0009 | g0093 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03579 | hp1 | a0001 | c0001 | t0037 | g0082 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03579 | hp2 | a0001 | c0001 | t0025 | g0031 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03654 | hp2 | a0001 | c0001 | t0063 | g0296 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03669 | hp2 | a0001 | c0001 | t0028 | g0071 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0313 | SAS | STU | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03688 | hp2 | a0001 | c0001 | t0006 | g0133 | SAS | STU | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0064 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03710 | hp2 | a0001 | c0001 | t0062 | g0143 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03831 | hp1 | a0001 | c0001 | t0049 | g0196 | SAS | BEB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03834 | hp1 | a0001 | c0001 | t0057 | g0124 | SAS | BEB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03834 | hp2 | a0001 | c0001 | t0013 | g0288 | SAS | BEB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03927 | hp1 | a0003 | c0007 | t0001 | g0147 | SAS | BEB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0324 | SAS | BEB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG04184 | hp2 | a0001 | c0001 | t0013 | g0131 | SAS | BEB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG04199 | hp1 | a0001 | c0001 | t0015 | g0117 | SAS | STU | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG04204 | hp1 | a0001 | c0001 | t0013 | g0186 | SAS | STU | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | STU | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | STU | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG04228 | hp2 | a0001 | c0001 | t0013 | g0185 | SAS | STU | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | CHB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18612 | hp2 | a0001 | c0001 | t0012 | g0151 | EAS | CHB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CHB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | CHB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0101 | AFR | YRI | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0044 | AFR | YRI | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18949 | hp1 | a0001 | c0001 | t0011 | g0301 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18953 | hp2 | a0001 | c0001 | t0017 | g0126 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18960 | hp1 | a0001 | c0001 | t0010 | g0120 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18960 | hp2 | a0001 | c0001 | t0012 | g0170 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18961 | hp1 | a0001 | c0001 | t0010 | g0121 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18961 | hp2 | a0001 | c0001 | t0050 | g0251 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18964 | hp2 | a0001 | c0001 | t0052 | g0169 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18966 | hp2 | a0001 | c0001 | t0007 | g0287 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18967 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18971 | hp1 | a0001 | c0001 | t0056 | g0317 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18971 | hp2 | a0001 | c0001 | t0014 | g0055 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18977 | hp2 | a0002 | c0009 | t0001 | g0248 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18979 | hp2 | a0001 | c0001 | t0010 | g0123 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18984 | hp1 | a0001 | c0001 | t0046 | g0182 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18984 | hp2 | a0001 | c0001 | t0011 | g0291 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19002 | hp1 | a0001 | c0001 | t0044 | g0139 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19010 | hp1 | a0001 | c0001 | t0030 | g0058 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19010 | hp2 | a0001 | c0001 | t0006 | g0158 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19011 | hp1 | a0001 | c0001 | t0040 | g0315 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19011 | hp2 | a0004 | c0005 | t0001 | g0162 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19030 | hp2 | a0001 | c0001 | t0009 | g0094 | AFR | LWK | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | LWK | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | LWK | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19055 | hp1 | a0001 | c0001 | t0041 | g0160 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19057 | hp1 | a0001 | c0001 | t0045 | g0200 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19063 | hp1 | a0001 | c0001 | t0010 | g0332 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19063 | hp2 | a0001 | c0001 | t0006 | g0125 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19064 | hp2 | a0001 | c0001 | t0006 | g0269 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19074 | hp1 | a0001 | c0001 | t0026 | g0081 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19074 | hp2 | a0001 | c0001 | t0007 | g0274 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19077 | hp1 | a0001 | c0001 | t0006 | g0309 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19086 | hp1 | a0001 | c0001 | t0011 | g0127 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19086 | hp2 | a0001 | c0001 | t0010 | g0119 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19091 | hp1 | a0001 | c0001 | t0010 | g0323 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | YRI | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA19240 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | YRI | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ASW | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA20129 | hp2 | a0001 | c0001 | t0034 | g0043 | AFR | ASW | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | TSI | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | TSI | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA20805 | hp1 | a0001 | c0001 | t0016 | g0054 | EUR | TSI | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0102 | EUR | TSI | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA20905 | hp1 | a0001 | c0001 | t0015 | g0114 | SAS | GIH | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA20905 | hp2 | a0001 | c0001 | t0016 | g0070 | SAS | GIH | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | CLM | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG01123 | hp2 | a0001 | c0001 | t0039 | g0145 | AMR | CLM | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0148 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0091 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0039 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG02559 | hp2 | a0001 | c0001 | t0008 | g0025 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03471 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG03471 | hp2 | a0001 | c0001 | t0029 | g0334 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | USA | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0083 | AFR | USA | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA20300 | hp1 | a0001 | c0001 | t0027 | g0045 | AFR | USA | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | USA | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0080 | AFR | LWK | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0088 | AFR | LWK | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
homoSapiens_chm13v2 | hp1 | a0001 | c0008 | t0054 | g0187 | REF | REF | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0016 | REF | REF | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:4657307
|
C | T | 1 | a0002 | 1 | NA18977.hp2 | stop_gained | HIGH | c.505C>T | p.Gln169* | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/17 | 640/3930 | 505/1731 | 169/576 | chr16 | 4657307 | ||
chr16:4657361
|
G | A | 1 | a0004 | 1 | NA19011.hp2 | missense_variant&splice_region_variant | MODERATE | c.559G>A | p.Glu187Lys | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/17 | 694/3930 | 559/1731 | 187/576 | chr16 | 4657361 | ||
chr16:4683252
|
C | T | 1 | a0003 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.1511C>T | p.Ser504Leu | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/17 | 1646/3930 | 1511/1731 | 504/576 | chr16 | 4683252 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:4650417
|
C | A | 2 | a0001c0002a0001c0004 | 5 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
synonymous_variant | LOW | c.141C>A | p.Pro47Pro | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/17 | 276/3930 | 141/1731 | 47/576 | chr16 | 4650417 | ||
chr16:4664744
|
A | G | 2 | a0001c0003a0001c0004 | 4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
synonymous_variant | LOW | c.597A>G | p.Val199Val | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 6/17 | 732/3930 | 597/1731 | 199/576 | chr16 | 4664744 | ||
chr16:4673551
|
C | T | 1 | a0001c0008 | 1 | homoSapiens_chm13v2.hp1 | synonymous_variant | LOW | c.849C>T | p.Ser283Ser | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/17 | 984/3930 | 849/1731 | 283/576 | chr16 | 4673551 | ||
chr16:4688884
|
C | T | 1 | a0001c0006 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1707C>T | p.Ser569Ser | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1842/3930 | 1707/1731 | 569/576 | chr16 | 4688884 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:4624953
|
C | G | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(36): Show | 231 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(228): Show |
5_prime_UTR_variant | MODIFIER | c.-8C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/17 | 8 | chr16 | 4624953 | |||||
chr16:4688919
|
G | A | 1 | a0001c0001t0039 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 11 | chr16 | 4688919 | |||||
chr16:4689176
|
T | C | 5 | a0001c0001t0019a0001c0001t0020a0001c0001t0021others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*268T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 268 | chr16 | 4689176 | |||||
chr16:4689188
|
G | A | 1 | a0001c0001t0024 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*280G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 280 | chr16 | 4689188 | |||||
chr16:4689245
|
A | C | 3 | a0001c0001t0062a0001c0001t0063a0001c0003t0018 | 4 | HG01167.hp1 HG01169.hp1 HG03654.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*337A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 337 | chr16 | 4689245 | |||||
chr16:4689377
|
C | G | 1 | a0001c0001t0015 | 4 | HG00738.hp2 HG02602.hp2 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*469C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 469 | chr16 | 4689377 | |||||
chr16:4689467
|
C | T | 5 | a0001c0001t0005a0001c0001t0023a0001c0001t0024others(2): Show | 17 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*559C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 559 | chr16 | 4689467 | |||||
chr16:4689513
|
T | C | 40 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(37): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*605T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 605 | chr16 | 4689513 | |||||
chr16:4689516
|
C | A | 2 | a0001c0001t0019a0001c0001t0025 | 2 | HG02622.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*608C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 608 | chr16 | 4689516 | |||||
chr16:4689518
|
C | G | 1 | a0001c0001t0061 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*610C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 610 | chr16 | 4689518 | |||||
chr16:4689638
|
C | T | 1 | a0001c0001t0060 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*730C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 730 | chr16 | 4689638 | |||||
chr16:4689674
|
A | G | 1 | a0001c0001t0037 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*766A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 766 | chr16 | 4689674 | |||||
chr16:4689767
|
CT | C | 31 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(28): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*874delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 874 | INFO_REALIGN_3_PRIME | chr16 | 4689767 | ||||
chr16:4689767
|
CTT | C | 5 | a0001c0001t0012a0001c0001t0026a0001c0001t0040others(2): Show | 9 | HG00323.hp2 HG01257.hp1 HG01975.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*873_*874delTT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 873 | INFO_REALIGN_3_PRIME | chr16 | 4689767 | ||||
chr16:4689784
|
A | T | 1 | a0001c0001t0059 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*876A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 876 | chr16 | 4689784 | |||||
chr16:4689806
|
C | T | 1 | a0001c0003t0018 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*898C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 898 | chr16 | 4689806 | |||||
chr16:4689822
|
G | A | 6 | a0001c0001t0025a0001c0001t0027a0001c0001t0042others(3): Show | 7 | HG01167.hp1 HG01169.hp1 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*914G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 914 | chr16 | 4689822 | |||||
chr16:4689851
|
C | T | 5 | a0001c0001t0009a0001c0001t0035a0001c0001t0058others(2): Show | 11 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*943C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 943 | chr16 | 4689851 | |||||
chr16:4690054
|
G | A | 1 | a0001c0001t0017 | 2 | HG00423.hp2 NA18953.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1146G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1146 | chr16 | 4690054 | |||||
chr16:4690060
|
G | A | 1 | a0001c0003t0018 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1152G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1152 | chr16 | 4690060 | |||||
chr16:4690096
|
G | A | 2 | a0001c0001t0025a0001c0003t0018 | 3 | HG01167.hp1 HG01169.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1188G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1188 | chr16 | 4690096 | |||||
chr16:4690163
|
T | G | 1 | a0001c0001t0050 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1255T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1255 | chr16 | 4690163 | |||||
chr16:4690164
|
C | T | 1 | a0001c0001t0050 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1256C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1256 | chr16 | 4690164 | |||||
chr16:4690170
|
C | T | 1 | a0001c0001t0057 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1262C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1262 | chr16 | 4690170 | |||||
chr16:4690207
|
T | G | 35 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(32): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*1299T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1299 | chr16 | 4690207 | |||||
chr16:4690285
|
C | G | 2 | a0001c0001t0010a0001c0001t0041 | 7 | NA18960.hp1 NA18961.hp1 NA18979.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1377C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1377 | chr16 | 4690285 | |||||
chr16:4690307
|
G | A | 1 | a0001c0003t0018 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1399G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1399 | chr16 | 4690307 | |||||
chr16:4690440
|
G | C | 38 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(35): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*1532G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1532 | chr16 | 4690440 | |||||
chr16:4690443
|
C | T | 36 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(33): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*1535C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1535 | chr16 | 4690443 | |||||
chr16:4690449
|
C | T | 1 | a0001c0001t0032 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1541C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1541 | chr16 | 4690449 | |||||
chr16:4690455
|
G | A | 1 | a0001c0001t0032 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1547G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1547 | chr16 | 4690455 | |||||
chr16:4690476
|
T | C | 43 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(40): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*1568T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1568 | chr16 | 4690476 | |||||
chr16:4690523
|
C | T | 1 | a0001c0001t0045 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1615C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1615 | chr16 | 4690523 | |||||
chr16:4690540
|
G | A | 1 | a0001c0001t0042 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1632G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1632 | chr16 | 4690540 | |||||
chr16:4690601
|
T | C | 44 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(41): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*1693T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1693 | chr16 | 4690601 | |||||
chr16:4690621
|
C | G | 1 | a0001c0001t0044 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1713C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1713 | chr16 | 4690621 | |||||
chr16:4690640
|
G | A | 1 | a0001c0001t0056 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1732G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1732 | chr16 | 4690640 | |||||
chr16:4690699
|
G | A | 1 | a0001c0001t0053 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1791G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1791 | chr16 | 4690699 | |||||
chr16:4690771
|
C | A | 1 | a0001c0001t0028 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1863C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1863 | chr16 | 4690771 | |||||
chr16:4690837
|
T | G | 1 | a0001c0001t0044 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1929T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1929 | chr16 | 4690837 | |||||
chr16:4690863
|
C | T | 1 | a0001c0001t0031 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1955C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1955 | chr16 | 4690863 | |||||
chr16:4690913
|
G | C | 1 | a0001c0001t0029 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2005G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 2005 | chr16 | 4690913 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:4625104
|
G | T | 2 | a0001c0001t0029g0334a0001c0001t0035g0333 | 2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.88+56G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625104 | ||||||
chr16:4625115
|
G | T | 251 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(248): Show | 251 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.88+67G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625115 | ||||||
chr16:4625191
|
A | G | 232 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(229): Show | 232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.88+143A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625191 | ||||||
chr16:4625202
|
C | T | 1 | a0001c0001t0010g0332 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.88+154C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625202 | ||||||
chr16:4625212
|
G | A | 1 | a0001c0002t0005g0001 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88+164G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625212 | ||||||
chr16:4625241
|
G | A | 1 | a0001c0001t0002g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.88+193G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625241 | ||||||
chr16:4625279
|
T | C | 231 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(228): Show | 231 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.88+231T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625279 | ||||||
chr16:4625291
|
C | T | 1 | a0001c0001t0004g0080 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.88+243C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625291 | ||||||
chr16:4625295
|
G | T | 2 | a0001c0001t0029g0334a0001c0001t0035g0333 | 2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.88+247G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625295 | ||||||
chr16:4625328
|
G | T | 2 | a0001c0001t0003g0078a0001c0001t0003g0079 | 2 | NA18977.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.88+280G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625328 | ||||||
chr16:4625371
|
G | T | 1 | a0001c0001t0003g0077 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.88+323G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625371 | ||||||
chr16:4625410
|
C | G | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG00408.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.88+362C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625410 | ||||||
chr16:4625413
|
A | G | 37 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0051others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.88+365A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625413 | ||||||
chr16:4625565
|
G | A | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.88+517G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625565 | ||||||
chr16:4625622
|
C | T | 1 | a0001c0001t0058g0329 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.88+574C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625622 | ||||||
chr16:4625713
|
G | A | 7 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0023g0006others(4): Show | 7 | HG01099.hp1 HG01884.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+665G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625713 | ||||||
chr16:4625721
|
C | G | 252 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(249): Show | 252 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.88+673C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625721 | ||||||
chr16:4625835
|
T | C | 297 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.88+787T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625835 | ||||||
chr16:4625875
|
T | C | 1 | a0001c0001t0002g0104 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.88+827T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625875 | ||||||
chr16:4625938
|
C | T | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.88+890C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625938 | ||||||
chr16:4625958
|
C | T | 297 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.88+910C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625958 | ||||||
chr16:4626008
|
G | C | 1 | a0001c0001t0037g0082 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.88+960G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626008 | ||||||
chr16:4626233
|
A | G | 1 | a0001c0001t0004g0080 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.88+1185A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626233 | ||||||
chr16:4626292
|
A | G | 1 | a0001c0001t0001g0328 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.88+1244A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626292 | ||||||
chr16:4626421
|
C | T | 332 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(329): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.88+1373C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626421 | ||||||
chr16:4626458
|
C | A | 1 | a0001c0002t0005g0001 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88+1410C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626458 | ||||||
chr16:4626488
|
C | T | 58 | a0001c0001t0001g0277a0001c0001t0001g0284a0001c0001t0001g0286others(55): Show | 58 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.88+1440C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626488 | ||||||
chr16:4626495
|
A | G | 1 | a0001c0002t0005g0001 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88+1447A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626495 | ||||||
chr16:4626525
|
G | A | 23 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0004g0017others(20): Show | 23 | HG01175.hp2 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.88+1477G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626525 | ||||||
chr16:4626548
|
C | G | 1 | a0001c0001t0001g0327 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.88+1500C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626548 | ||||||
chr16:4626555
|
A | T | 2 | a0001c0001t0003g0007a0001c0001t0003g0008 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.88+1507A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626555 | ||||||
chr16:4626593
|
C | T | 1 | a0001c0001t0002g0326 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.88+1545C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626593 | ||||||
chr16:4626594
|
A | G | 300 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(297): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.88+1546A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626594 | ||||||
chr16:4626613
|
G | T | 37 | a0001c0001t0001g0103a0001c0001t0003g0047a0001c0001t0003g0048others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.88+1565G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626613 | ||||||
chr16:4626633
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.88+1585A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626633 | ||||||
chr16:4626659
|
G | A | 230 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(227): Show | 230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.88+1611G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626659 | ||||||
chr16:4626719
|
A | G | 13 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0005g0036others(10): Show | 13 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+1671A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626719 | ||||||
chr16:4626729
|
C | G | 230 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(227): Show | 230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.88+1681C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626729 | ||||||
chr16:4626734
|
C | T | 3 | a0001c0001t0003g0013a0001c0001t0020g0012a0001c0001t0022g0014 | 3 | HG02723.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.88+1686C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626734 | ||||||
chr16:4626793
|
A | G | 13 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0005g0036others(10): Show | 13 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+1745A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626793 | ||||||
chr16:4626851
|
C | A | 69 | a0001c0001t0001g0103a0001c0001t0003g0009a0001c0001t0003g0013others(66): Show | 69 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.88+1803C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626851 | ||||||
chr16:4626868
|
G | C | 14 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0005g0036others(11): Show | 14 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+1820G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626868 | ||||||
chr16:4626903
|
C | G | 313 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.88+1855C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626903 | ||||||
chr16:4626971
|
G | A | 66 | a0001c0001t0001g0103a0001c0001t0003g0009a0001c0001t0003g0013others(63): Show | 66 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.88+1923G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626971 | ||||||
chr16:4627039
|
C | T | 15 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0004g0089others(12): Show | 15 | HG01175.hp2 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.88+1991C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627039 | ||||||
chr16:4627050
|
C | T | 10 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263others(7): Show | 10 | HG00673.hp2 HG02074.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.88+2002C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627050 | ||||||
chr16:4627080
|
G | T | 2 | a0001c0001t0008g0100a0001c0001t0009g0101 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.88+2032G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627080 | ||||||
chr16:4627189
|
C | T | 228 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(225): Show | 228 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.88+2141C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627189 | ||||||
chr16:4627401
|
A | G | 1 | a0001c0001t0002g0260 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.88+2353A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627401 | ||||||
chr16:4627417
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.88+2369T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627417 | ||||||
chr16:4627433
|
G | A | 2 | a0001c0001t0029g0334a0001c0001t0035g0333 | 2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.88+2385G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627433 | ||||||
chr16:4627496
|
G | C | 238 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(235): Show | 238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.88+2448G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627496 | ||||||
chr16:4627510
|
A | G | 4 | a0001c0001t0003g0074a0001c0001t0004g0017a0001c0001t0023g0006others(1): Show | 4 | HG02809.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+2462A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627510 | ||||||
chr16:4627514
|
G | A | 1 | a0001c0001t0034g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.88+2466G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627514 | ||||||
chr16:4627525
|
C | T | 6 | a0001c0001t0001g0270a0001c0001t0002g0253a0001c0001t0002g0260others(3): Show | 6 | HG00673.hp1 HG02056.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+2477C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627525 | ||||||
chr16:4627530
|
A | G | 1 | a0001c0001t0053g0322 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.88+2482A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627530 | ||||||
chr16:4627539
|
TCACTTTG others(592): Show |
T | 1 | a0001c0001t0005g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.88+2506_88+3104del | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4627539 | |||||
chr16:4627548
|
G | A | 2 | a0001c0001t0002g0272a0001c0001t0002g0326 | 2 | HG00639.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.88+2500G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627548 | ||||||
chr16:4627558
|
C | T | 1 | a0001c0001t0002g0250 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.88+2510C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627558 | ||||||
chr16:4627583
|
G | C | 7 | a0001c0001t0003g0009a0001c0001t0021g0042a0001c0001t0029g0334others(4): Show | 7 | HG02572.hp2 HG02896.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+2535G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627583 | ||||||
chr16:4627583
|
G | T | 40 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(37): Show | 40 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.88+2535G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627583 | ||||||
chr16:4627591
|
T | G | 3 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0034g0043 | 3 | HG02486.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.88+2543T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627591 | ||||||
chr16:4627598
|
T | C | 72 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0111others(69): Show | 72 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.88+2550T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627598 | ||||||
chr16:4627603
|
C | A | 61 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0111others(58): Show | 61 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.88+2555C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627603 | ||||||
chr16:4627603
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.88+2555C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627603 | ||||||
chr16:4627606
|
G | T | 82 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0108others(79): Show | 82 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.88+2558G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627606 | ||||||
chr16:4627624
|
A | G | 1 | a0001c0001t0008g0035 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.88+2576A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627624 | ||||||
chr16:4627658
|
A | G | 1 | a0001c0002t0003g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.88+2610A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627658 | ||||||
chr16:4627660
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.88+2612G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627660 | ||||||
chr16:4627679
|
C | T | 2 | a0001c0001t0029g0334a0001c0001t0035g0333 | 2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.88+2631C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627679 | ||||||
chr16:4627744
|
T | G | 20 | a0001c0001t0002g0105a0001c0001t0003g0007a0001c0001t0003g0008others(17): Show | 20 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.88+2696T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627744 | ||||||
chr16:4627749
|
C | T | 1 | a0001c0001t0003g0009 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.88+2701C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627749 | ||||||
chr16:4627975
|
G | C | 1 | a0001c0001t0002g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.88+2927G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627975 | ||||||
chr16:4628077
|
C | A | 1 | a0001c0001t0002g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.88+3029C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628077 | ||||||
chr16:4628079
|
C | CA | 11 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0261others(8): Show | 11 | HG00280.hp2 HG01192.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.88+3049dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4628079 | |||||
chr16:4628079
|
CA | C | 9 | a0001c0001t0001g0241a0001c0001t0002g0242a0001c0001t0002g0243others(6): Show | 9 | HG01167.hp2 HG02273.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+3049delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4628079 | |||||
chr16:4628114
|
C | T | 7 | a0001c0001t0001g0239a0001c0001t0001g0244a0001c0001t0002g0237others(4): Show | 7 | HG00140.hp1 HG00741.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+3066C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628114 | ||||||
chr16:4628116
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.88+3068G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628116 | ||||||
chr16:4628255
|
A | T | 1 | a0001c0002t0005g0001 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88+3207A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628255 | ||||||
chr16:4628385
|
C | CA | 7 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(4): Show | 7 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+3355dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4628385 | |||||
chr16:4628385
|
CA | C | 277 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.88+3355delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4628385 | |||||
chr16:4628410
|
G | T | 2 | a0001c0001t0004g0011a0001c0001t0019g0010 | 2 | HG01243.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.88+3362G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628410 | ||||||
chr16:4628432
|
A | C | 4 | a0001c0001t0002g0236a0001c0001t0002g0243a0001c0001t0034g0043others(1): Show | 4 | HG01167.hp2 NA18940.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+3384A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628432 | ||||||
chr16:4628463
|
G | T | 1 | a0001c0001t0003g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.88+3415G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628463 | ||||||
chr16:4628475
|
C | G | 1 | a0001c0001t0034g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.88+3427C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628475 | ||||||
chr16:4628496
|
C | G | 1 | a0001c0001t0001g0108 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.88+3448C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628496 | ||||||
chr16:4628546
|
T | G | 6 | a0001c0001t0001g0239a0001c0001t0002g0237a0001c0001t0002g0240others(3): Show | 6 | HG00140.hp1 HG00741.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+3498T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628546 | ||||||
chr16:4628692
|
G | A | 1 | a0001c0001t0044g0139 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.88+3644G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628692 | ||||||
chr16:4628770
|
C | G | 1 | a0001c0001t0002g0242 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.88+3722C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628770 | ||||||
chr16:4629029
|
G | T | 1 | a0001c0002t0003g0005 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.88+3981G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629029 | ||||||
chr16:4629147
|
C | CGTGTGT | 3 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0028g0071 | 3 | HG02055.hp2 HG02258.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.88+4101_88+4102ins others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629147 | |||||
chr16:4629148
|
G | GTA | 6 | a0001c0001t0002g0105a0001c0001t0004g0011a0001c0001t0005g0044others(3): Show | 6 | HG01243.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+4102_88+4103dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629148 | |||||
chr16:4629150
|
A | ATATT | 9 | a0001c0001t0003g0009a0001c0001t0005g0036a0001c0001t0005g0037others(6): Show | 9 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+4103_88+4104ins others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | |||||
chr16:4629150
|
A | ATATTGTG others(6): Show |
1 | a0001c0004t0036g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.88+4103_88+4104ins others(13): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | |||||
chr16:4629150
|
A | ATATTTGT others(3): Show |
3 | a0001c0002t0003g0005a0001c0002t0004g0003a0001c0002t0005g0001 | 3 | HG01099.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.88+4103_88+4104ins others(10): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | |||||
chr16:4629150
|
A | ATATTTGT others(5): Show |
1 | a0001c0001t0021g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.88+4103_88+4104ins others(12): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | |||||
chr16:4629150
|
A | ATG | 58 | a0001c0001t0001g0111a0001c0001t0001g0161a0001c0001t0001g0163others(55): Show | 58 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.88+4143_88+4144dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | |||||
chr16:4629150
|
A | ATGTG | 66 | a0001c0001t0001g0107a0001c0001t0001g0113a0001c0001t0001g0115others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.88+4141_88+4144dup others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | |||||
chr16:4629150
|
A | ATGTGTG | 48 | a0001c0001t0001g0106a0001c0001t0001g0122a0001c0001t0001g0128others(45): Show | 48 | HG00408.hp2 HG00673.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.88+4139_88+4144dup others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | |||||
chr16:4629150
|
A | ATGTGTGT others(1): Show |
16 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(13): Show | 16 | HG00558.hp1 HG00621.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.88+4137_88+4144dup others(8): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | |||||
chr16:4629150
|
A | ATGTGTGT others(3): Show |
5 | a0001c0001t0001g0261a0001c0001t0001g0271a0001c0001t0002g0102others(2): Show | 5 | HG02300.hp2 HG02976.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+4135_88+4144dup others(10): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | |||||
chr16:4629150
|
A | ATGTGTGT others(5): Show |
2 | a0001c0001t0003g0007a0001c0001t0003g0008 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.88+4133_88+4144dup others(12): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | |||||
chr16:4629150
|
A | G | 8 | a0001c0001t0001g0129a0001c0001t0002g0234a0001c0001t0002g0235others(5): Show | 8 | HG00639.hp2 HG01167.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+4102A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629150 | ||||||
chr16:4629150
|
ATG | A | 9 | a0001c0001t0007g0303a0001c0001t0008g0022a0001c0001t0008g0023others(6): Show | 9 | HG00597.hp1 HG01884.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.88+4143_88+4144del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | |||||
chr16:4629150
|
ATGTG | A | 10 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0279others(7): Show | 10 | HG00738.hp1 HG01081.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.88+4141_88+4144del others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | |||||
chr16:4629150
|
ATGTGTG | A | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0003g0078others(1): Show | 4 | NA18975.hp1 NA18977.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+4139_88+4144del others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | |||||
chr16:4629150
|
ATGTGTGT others(1): Show |
A | 35 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(32): Show | 35 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.88+4137_88+4144del others(8): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | |||||
chr16:4629150
|
ATGTGTGT others(3): Show |
A | 3 | a0001c0001t0003g0074a0001c0001t0007g0148a0003c0007t0001g0147 | 3 | HG02109.hp1 HG02809.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.88+4135_88+4144del others(10): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | |||||
chr16:4629150
|
ATGTGTGT others(5): Show |
A | 1 | a0001c0001t0002g0237 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.88+4133_88+4144del others(12): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | |||||
chr16:4629152
|
G | A | 8 | a0001c0001t0003g0013a0001c0001t0005g0083a0001c0001t0014g0019others(5): Show | 8 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+4104G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629152 | ||||||
chr16:4629152
|
G | T | 6 | a0001c0001t0002g0105a0001c0001t0004g0011a0001c0001t0005g0044others(3): Show | 6 | HG01243.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+4104G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629152 | ||||||
chr16:4629154
|
G | A | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.88+4106G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629154 | ||||||
chr16:4629154
|
G | T | 8 | a0001c0001t0003g0013a0001c0001t0005g0083a0001c0001t0014g0019others(5): Show | 8 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+4106G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629154 | ||||||
chr16:4629156
|
G | A | 4 | a0001c0001t0004g0017a0001c0001t0023g0006a0001c0001t0027g0045others(1): Show | 4 | HG02922.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+4108G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629156 | ||||||
chr16:4629156
|
G | T | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.88+4108G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629156 | ||||||
chr16:4629158
|
G | A | 2 | a0001c0001t0003g0078a0001c0001t0003g0079 | 2 | NA18977.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.88+4110G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629158 | ||||||
chr16:4629158
|
G | T | 4 | a0001c0001t0004g0017a0001c0001t0023g0006a0001c0001t0027g0045others(1): Show | 4 | HG02922.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+4110G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629158 | ||||||
chr16:4629160
|
G | A | 35 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(32): Show | 35 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.88+4112G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629160 | ||||||
chr16:4629160
|
G | T | 2 | a0001c0001t0003g0078a0001c0001t0003g0079 | 2 | NA18977.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.88+4112G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629160 | ||||||
chr16:4629162
|
G | A | 1 | a0001c0001t0003g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.88+4114G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629162 | ||||||
chr16:4629162
|
G | T | 35 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(32): Show | 35 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.88+4114G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629162 | ||||||
chr16:4629164
|
G | T | 1 | a0001c0001t0003g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.88+4116G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629164 | ||||||
chr16:4629191
|
T | A | 1 | a0001c0001t0014g0019 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.88+4143T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629191 | ||||||
chr16:4629236
|
ATTGT | A | 7 | a0001c0001t0003g0098a0001c0001t0008g0022a0001c0001t0008g0023others(4): Show | 7 | HG02559.hp2 HG02896.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+4191_88+4194del others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629236 | |||||
chr16:4629273
|
A | C | 3 | a0001c0001t0002g0105a0001c0001t0004g0011a0001c0001t0019g0010 | 3 | HG01243.hp1 HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.88+4225A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629273 | ||||||
chr16:4629467
|
A | G | 66 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(63): Show | 66 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.88+4419A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629467 | ||||||
chr16:4629511
|
T | C | 12 | a0001c0001t0003g0013a0001c0001t0004g0017a0001c0001t0005g0044others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.88+4463T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629511 | ||||||
chr16:4629600
|
G | A | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.88+4552G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629600 | ||||||
chr16:4629610
|
A | G | 15 | a0001c0001t0002g0105a0001c0001t0003g0009a0001c0001t0005g0036others(12): Show | 15 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.88+4562A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629610 | ||||||
chr16:4629627
|
T | A | 37 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(34): Show | 37 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.88+4579T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629627 | ||||||
chr16:4629628
|
G | A | 72 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(69): Show | 72 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.88+4580G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629628 | ||||||
chr16:4629661
|
C | A | 1 | a0001c0001t0003g0077 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.88+4613C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629661 | ||||||
chr16:4629693
|
C | T | 1 | a0001c0002t0005g0001 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88+4645C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629693 | ||||||
chr16:4629737
|
C | CA | 17 | a0001c0001t0001g0136a0001c0001t0001g0168a0001c0001t0001g0204others(14): Show | 17 | HG00735.hp2 HG00738.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.88+4705dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629737 | |||||
chr16:4629737
|
CA | C | 19 | a0001c0001t0001g0201a0001c0001t0001g0265a0001c0001t0002g0105others(16): Show | 19 | HG00558.hp1 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.88+4705delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629737 | |||||
chr16:4629853
|
C | G | 1 | a0001c0001t0034g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.88+4805C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629853 | ||||||
chr16:4629875
|
G | A | 3 | a0001c0001t0004g0017a0001c0001t0023g0006a0001c0003t0038g0018 | 3 | HG02922.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.88+4827G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629875 | ||||||
chr16:4629913
|
G | A | 1 | a0001c0001t0002g0306 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.88+4865G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629913 | ||||||
chr16:4629950
|
T | G | 59 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(56): Show | 59 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.88+4902T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629950 | ||||||
chr16:4630048
|
C | CA | 55 | a0001c0001t0001g0129a0001c0001t0001g0136a0001c0001t0001g0137others(52): Show | 55 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.88+5021dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630048 | |||||
chr16:4630048
|
C | CAA | 7 | a0001c0001t0002g0258a0001c0001t0003g0034a0001c0001t0004g0017others(4): Show | 7 | HG00099.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+5020_88+5021dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630048 | |||||
chr16:4630048
|
CA | C | 13 | a0001c0001t0001g0122a0001c0001t0001g0128a0001c0001t0001g0222others(10): Show | 13 | HG02015.hp2 HG02080.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.88+5021delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630048 | |||||
chr16:4630048
|
CAAA | C | 14 | a0001c0001t0002g0105a0001c0001t0003g0009a0001c0001t0005g0036others(11): Show | 14 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.88+5019_88+5021del others(3): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630048 | |||||
chr16:4630072
|
G | C | 65 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(62): Show | 65 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.88+5024G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630072 | ||||||
chr16:4630077
|
T | A | 1 | a0001c0001t0011g0291 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.88+5029T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630077 | ||||||
chr16:4630087
|
C | T | 1 | a0001c0001t0003g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.88+5039C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630087 | ||||||
chr16:4630088
|
G | A | 1 | a0001c0004t0036g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.88+5040G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630088 | ||||||
chr16:4630128
|
G | C | 38 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(35): Show | 38 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.88+5080G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630128 | ||||||
chr16:4630198
|
A | C | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+5150A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630198 | ||||||
chr16:4630252
|
C | T | 9 | a0001c0001t0003g0013a0001c0001t0005g0044a0001c0001t0005g0083others(6): Show | 9 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+5204C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630252 | ||||||
chr16:4630283
|
C | G | 67 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(64): Show | 67 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.88+5235C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630283 | ||||||
chr16:4630354
|
C | CA | 59 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.88+5319dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630354 | |||||
chr16:4630354
|
C | CAA | 10 | a0001c0001t0003g0013a0001c0001t0003g0053a0001c0001t0005g0044others(7): Show | 10 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.88+5318_88+5319dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630354 | |||||
chr16:4630438
|
TTTGTTG | T | 28 | a0001c0001t0002g0105a0001c0001t0003g0009a0001c0001t0003g0013others(25): Show | 28 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.88+5406_88+5411del others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630438 | |||||
chr16:4630448
|
T | C | 2 | a0001c0001t0002g0308a0001c0001t0047g0283 | 2 | HG00408.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.88+5400T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630448 | ||||||
chr16:4630493
|
C | G | 1 | a0001c0001t0003g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.88+5445C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630493 | ||||||
chr16:4630531
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.88+5483G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630531 | ||||||
chr16:4630570
|
A | G | 5 | a0001c0001t0005g0044a0001c0001t0005g0083a0001c0001t0005g0084others(2): Show | 5 | HG02280.hp1 HG02886.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+5522A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630570 | ||||||
chr16:4630604
|
C | T | 5 | a0001c0001t0005g0044a0001c0001t0005g0083a0001c0001t0005g0084others(2): Show | 5 | HG02280.hp1 HG02886.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+5556C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630604 | ||||||
chr16:4630638
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0223 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.88+5590G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630638 | ||||||
chr16:4630673
|
C | G | 1 | a0001c0001t0003g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.88+5625C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630673 | ||||||
chr16:4630678
|
C | G | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+5630C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630678 | ||||||
chr16:4630731
|
C | T | 94 | a0001c0001t0001g0284a0001c0001t0001g0286a0001c0001t0001g0311others(91): Show | 94 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.88+5683C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630731 | ||||||
chr16:4630760
|
A | G | 37 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(34): Show | 37 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.88+5712A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630760 | ||||||
chr16:4630808
|
C | CT | 10 | a0001c0001t0001g0118a0001c0001t0001g0136a0001c0001t0001g0204others(7): Show | 10 | HG00735.hp2 HG01243.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.88+5780dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630808 | |||||
chr16:4630808
|
CT | C | 28 | a0001c0001t0001g0217a0001c0001t0001g0223a0001c0001t0001g0241others(25): Show | 28 | HG01167.hp2 HG01975.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.88+5780delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630808 | |||||
chr16:4630808
|
CTT | C | 10 | a0001c0001t0003g0013a0001c0001t0005g0044a0001c0001t0005g0083others(7): Show | 10 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.88+5779_88+5780del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630808 | |||||
chr16:4630875
|
G | A | 1 | a0001c0001t0021g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.88+5827G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630875 | ||||||
chr16:4631108
|
C | T | 2 | a0001c0001t0004g0017a0001c0003t0038g0018 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.88+6060C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631108 | ||||||
chr16:4631183
|
G | A | 2 | a0001c0001t0004g0050a0001c0001t0004g0067 | 2 | HG00099.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.88+6135G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631183 | ||||||
chr16:4631308
|
A | G | 12 | a0001c0001t0003g0013a0001c0001t0004g0017a0001c0001t0005g0044others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.88+6260A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631308 | ||||||
chr16:4631507
|
G | A | 67 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(64): Show | 67 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.88+6459G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631507 | ||||||
chr16:4631588
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.88+6540C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631588 | ||||||
chr16:4631629
|
A | G | 2 | a0001c0001t0003g0013a0001c0001t0022g0014 | 2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.88+6581A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631629 | ||||||
chr16:4631709
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.88+6661T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631709 | ||||||
chr16:4631746
|
C | G | 1 | a0001c0002t0005g0001 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88+6698C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631746 | ||||||
chr16:4631796
|
T | C | 1 | a0001c0001t0014g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.88+6748T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631796 | ||||||
chr16:4631845
|
C | G | 11 | a0001c0001t0002g0105a0001c0001t0004g0017a0001c0001t0005g0036others(8): Show | 11 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.88+6797C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631845 | ||||||
chr16:4631902
|
A | AGTT | 241 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0111others(238): Show | 241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.88+6858_88+6860dup others(3): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4631902 | |||||
chr16:4631906
|
G | GTTGT | 6 | a0001c0001t0001g0193a0001c0001t0001g0201a0001c0001t0001g0231others(3): Show | 6 | HG01106.hp1 HG01243.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+6860_88+6861ins others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4631906 | |||||
chr16:4631907
|
T | TTG | 63 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(60): Show | 63 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.88+6860_88+6861ins others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4631907 | |||||
chr16:4631908
|
T | TG | 9 | a0001c0001t0003g0013a0001c0001t0005g0044a0001c0001t0005g0083others(6): Show | 9 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+6860_88+6861ins others(1): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631908 | ||||||
chr16:4631961
|
A | G | 1 | a0001c0001t0002g0259 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.88+6913A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631961 | ||||||
chr16:4632007
|
C | CT | 42 | a0001c0001t0001g0122a0001c0001t0001g0129a0001c0001t0001g0134others(39): Show | 42 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.88+6983dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4632007 | |||||
chr16:4632007
|
C | CTTTT | 13 | a0001c0001t0001g0217a0001c0001t0002g0105a0001c0001t0002g0142others(10): Show | 13 | HG01243.hp1 HG02258.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+6980_88+6983dup others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4632007 | |||||
chr16:4632007
|
C | CTTTTT | 21 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0002g0171others(18): Show | 21 | HG00544.hp1 HG00673.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.88+6979_88+6983dup others(5): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4632007 | |||||
chr16:4632007
|
CT | C | 36 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(33): Show | 36 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.88+6983delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4632007 | |||||
chr16:4632007
|
CTTTT | C | 9 | a0001c0001t0003g0013a0001c0001t0005g0044a0001c0001t0005g0083others(6): Show | 9 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+6980_88+6983del others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4632007 | |||||
chr16:4632035
|
A | G | 1 | a0001c0001t0006g0157 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.88+6987A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632035 | ||||||
chr16:4632091
|
T | G | 1 | a0001c0001t0021g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.88+7043T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632091 | ||||||
chr16:4632106
|
G | C | 74 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(71): Show | 74 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.88+7058G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632106 | ||||||
chr16:4632127
|
C | T | 1 | a0001c0001t0028g0071 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.88+7079C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632127 | ||||||
chr16:4632143
|
T | A | 73 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(70): Show | 73 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.88+7095T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632143 | ||||||
chr16:4632205
|
T | TG | 332 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(329): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.88+7160dupG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4632205 | |||||
chr16:4632215
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.88+7167C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632215 | ||||||
chr16:4632254
|
C | T | 79 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(76): Show | 79 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.88+7206C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632254 | ||||||
chr16:4632286
|
TTACAGGC | T | 36 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(33): Show | 36 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.88+7239_88+7245del others(7): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632286 | ||||||
chr16:4632310
|
G | A | 3 | a0001c0001t0003g0009a0001c0001t0029g0334a0001c0001t0035g0333 | 3 | HG02572.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.88+7262G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632310 | ||||||
chr16:4632416
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.88+7368C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632416 | ||||||
chr16:4632444
|
A | T | 1 | a0001c0001t0020g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.88+7396A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632444 | ||||||
chr16:4632455
|
G | A | 2 | a0001c0002t0003g0004a0001c0002t0004g0003 | 2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.88+7407G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632455 | ||||||
chr16:4632465
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0212 | 2 | HG00735.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.88+7417C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632465 | ||||||
chr16:4632486
|
C | T | 43 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(40): Show | 43 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.88+7438C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632486 | ||||||
chr16:4632542
|
C | T | 13 | a0001c0001t0002g0105a0001c0001t0004g0017a0001c0001t0005g0036others(10): Show | 13 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+7494C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632542 | ||||||
chr16:4632630
|
T | G | 74 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(71): Show | 74 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.88+7582T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632630 | ||||||
chr16:4632661
|
G | A | 1 | a0001c0001t0021g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.88+7613G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632661 | ||||||
chr16:4632696
|
G | T | 1 | a0001c0001t0003g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.88+7648G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632696 | ||||||
chr16:4632740
|
A | C | 1 | a0001c0001t0002g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.88+7692A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632740 | ||||||
chr16:4632800
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+7752C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632800 | ||||||
chr16:4632802
|
G | A | 1 | a0001c0006t0009g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.88+7754G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632802 | ||||||
chr16:4633106
|
G | T | 1 | a0001c0001t0002g0259 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.88+8058G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633106 | ||||||
chr16:4633125
|
C | T | 2 | a0001c0001t0029g0334a0001c0001t0035g0333 | 2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.88+8077C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633125 | ||||||
chr16:4633126
|
A | G | 74 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(71): Show | 74 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.88+8078A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633126 | ||||||
chr16:4633225
|
T | TA | 11 | a0001c0001t0004g0017a0001c0001t0005g0036a0001c0001t0005g0037others(8): Show | 11 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.88+8182dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4633225 | |||||
chr16:4633250
|
G | A | 1 | a0001c0001t0007g0159 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.88+8202G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633250 | ||||||
chr16:4633336
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.88+8288C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633336 | ||||||
chr16:4633463
|
G | C | 3 | a0001c0001t0014g0019a0001c0001t0014g0020a0001c0001t0033g0021 | 3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.88+8415G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633463 | ||||||
chr16:4633548
|
G | A | 1 | a0001c0001t0059g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.88+8500G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633548 | ||||||
chr16:4633718
|
AT | A | 13 | a0001c0001t0001g0277a0001c0001t0002g0105a0001c0001t0004g0017others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+8672delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4633718 | |||||
chr16:4633719
|
T | A | 41 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(38): Show | 41 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+8671T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633719 | ||||||
chr16:4633720
|
T | A | 54 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(51): Show | 54 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.88+8672T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633720 | ||||||
chr16:4633773
|
A | C | 6 | a0001c0001t0003g0098a0001c0002t0003g0004a0001c0002t0003g0005others(3): Show | 6 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+8725A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633773 | ||||||
chr16:4633781
|
T | G | 1 | a0001c0001t0062g0143 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.88+8733T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633781 | ||||||
chr16:4633784
|
C | A | 1 | a0001c0001t0062g0143 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.88+8736C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633784 | ||||||
chr16:4633810
|
C | T | 2 | a0001c0001t0011g0290a0001c0001t0061g0294 | 2 | HG02735.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.88+8762C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633810 | ||||||
chr16:4633871
|
C | A | 1 | a0001c0001t0001g0270 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.88+8823C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633871 | ||||||
chr16:4633879
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.88+8831G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633879 | ||||||
chr16:4633879
|
G | C | 1 | a0001c0001t0001g0265 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.88+8831G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633879 | ||||||
chr16:4633881
|
C | G | 1 | a0001c0001t0001g0265 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.88+8833C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633881 | ||||||
chr16:4633883
|
A | C | 1 | a0001c0001t0001g0265 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.88+8835A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633883 | ||||||
chr16:4634041
|
A | C | 1 | a0001c0001t0021g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.88+8993A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634041 | ||||||
chr16:4634131
|
G | A | 1 | a0001c0001t0021g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.88+9083G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634131 | ||||||
chr16:4634247
|
A | T | 1 | a0001c0001t0001g0265 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.88+9199A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634247 | ||||||
chr16:4634268
|
C | G | 42 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(39): Show | 42 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.88+9220C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634268 | ||||||
chr16:4634293
|
G | A | 3 | a0001c0001t0002g0282a0001c0001t0002g0314a0001c0001t0010g0323 | 3 | HG02027.hp1 NA19080.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.88+9245G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634293 | ||||||
chr16:4634384
|
G | T | 4 | a0001c0001t0002g0105a0001c0001t0004g0017a0001c0001t0019g0010others(1): Show | 4 | HG02622.hp2 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+9336G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634384 | ||||||
chr16:4634399
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+9351C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634399 | ||||||
chr16:4634410
|
T | A | 2 | a0001c0001t0002g0153a0001c0001t0041g0160 | 2 | NA18975.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.88+9362T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634410 | ||||||
chr16:4634447
|
G | A | 70 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(67): Show | 70 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.88+9399G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634447 | ||||||
chr16:4634504
|
G | A | 1 | a0001c0001t0040g0315 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.88+9456G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634504 | ||||||
chr16:4634575
|
C | T | 1 | a0001c0002t0003g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.88+9527C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634575 | ||||||
chr16:4634584
|
GC | G | 9 | a0001c0001t0003g0013a0001c0001t0005g0044a0001c0001t0005g0083others(6): Show | 9 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+9539delC | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4634584 | |||||
chr16:4634596
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0212 | 2 | HG00735.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.88+9548G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634596 | ||||||
chr16:4634777
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+9729C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634777 | ||||||
chr16:4634830
|
G | A | 1 | a0004c0005t0001g0162 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.88+9782G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634830 | ||||||
chr16:4634928
|
C | T | 1 | a0001c0001t0004g0062 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.88+9880C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634928 | ||||||
chr16:4634971
|
C | A | 2 | a0001c0001t0011g0290a0001c0001t0061g0294 | 2 | HG02735.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.88+9923C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634971 | ||||||
chr16:4635042
|
G | C | 1 | a0001c0001t0006g0157 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.88+9994G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635042 | ||||||
chr16:4635110
|
A | G | 4 | a0001c0001t0004g0017a0001c0001t0008g0025a0001c0001t0023g0006others(1): Show | 4 | HG02559.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+10062A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635110 | ||||||
chr16:4635325
|
G | C | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+10277G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635325 | ||||||
chr16:4635482
|
T | G | 1 | a0001c0001t0003g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.88+10434T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635482 | ||||||
chr16:4635488
|
G | A | 1 | a0001c0001t0034g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.88+10440G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635488 | ||||||
chr16:4635569
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.88+10521G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635569 | ||||||
chr16:4635617
|
C | T | 63 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.88+10569C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635617 | ||||||
chr16:4635714
|
A | G | 1 | a0001c0001t0007g0167 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.88+10666A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635714 | ||||||
chr16:4635746
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+10698C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635746 | ||||||
chr16:4635791
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+10743C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635791 | ||||||
chr16:4635801
|
A | AT | 69 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0113others(66): Show | 69 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.88+10772dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4635801 | |||||
chr16:4635801
|
A | ATT | 24 | a0001c0001t0002g0105a0001c0001t0002g0141a0001c0001t0003g0060others(21): Show | 24 | HG00544.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.88+10771_88+10772d others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4635801 | |||||
chr16:4635877
|
G | C | 1 | a0001c0001t0031g0046 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.88+10829G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635877 | ||||||
chr16:4635937
|
T | C | 7 | a0001c0001t0003g0009a0001c0001t0014g0019a0001c0001t0014g0020others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+10889T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635937 | ||||||
chr16:4635968
|
G | GT | 71 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.88+10932dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4635968 | |||||
chr16:4635968
|
G | GTT | 13 | a0001c0001t0002g0105a0001c0001t0002g0235a0001c0001t0004g0017others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+10931_88+10932d others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4635968 | |||||
chr16:4636084
|
G | T | 7 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0001g0191others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+11036G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636084 | ||||||
chr16:4636192
|
G | A | 1 | a0001c0001t0009g0090 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.88+11144G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636192 | ||||||
chr16:4636215
|
A | G | 14 | a0001c0001t0002g0105a0001c0001t0004g0017a0001c0001t0005g0036others(11): Show | 14 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+11167A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636215 | ||||||
chr16:4636267
|
C | G | 1 | a0001c0001t0010g0323 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.88+11219C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636267 | ||||||
chr16:4636275
|
C | T | 6 | a0001c0001t0003g0098a0001c0002t0003g0004a0001c0002t0003g0005others(3): Show | 6 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+11227C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636275 | ||||||
chr16:4636359
|
G | C | 1 | a0001c0001t0001g0108 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.88+11311G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636359 | ||||||
chr16:4636410
|
G | A | 1 | a0001c0001t0002g0208 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.88+11362G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636410 | ||||||
chr16:4636439
|
C | T | 1 | a0001c0001t0016g0070 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.88+11391C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636439 | ||||||
chr16:4636468
|
A | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0205 | 2 | NA18967.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.88+11420A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636468 | ||||||
chr16:4636567
|
C | T | 3 | a0001c0001t0002g0174a0001c0001t0042g0189a0001c0001t0043g0190 | 3 | HG02630.hp2 HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.88+11519C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636567 | ||||||
chr16:4636688
|
T | G | 1 | a0001c0002t0003g0005 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.88+11640T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636688 | ||||||
chr16:4636740
|
T | C | 1 | a0001c0001t0034g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.88+11692T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636740 | ||||||
chr16:4636806
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0223 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.88+11758G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636806 | ||||||
chr16:4636843
|
G | T | 7 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+11795G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636843 | ||||||
chr16:4636987
|
C | T | 1 | a0001c0001t0007g0303 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.88+11939C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636987 | ||||||
chr16:4637049
|
G | C | 6 | a0001c0001t0003g0009a0001c0001t0014g0019a0001c0001t0014g0020others(3): Show | 6 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+12001G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637049 | ||||||
chr16:4637118
|
C | CA | 26 | a0001c0001t0001g0108a0001c0001t0001g0136a0001c0001t0001g0163others(23): Show | 26 | HG01123.hp2 HG01258.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.88+12093dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4637118 | |||||
chr16:4637118
|
CA | C | 16 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0205others(13): Show | 16 | HG00323.hp1 HG01070.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.88+12093delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4637118 | |||||
chr16:4637238
|
C | T | 7 | a0001c0001t0001g0188a0001c0001t0001g0204a0001c0001t0001g0212others(4): Show | 7 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+12190C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637238 | ||||||
chr16:4637306
|
T | A | 3 | a0001c0001t0014g0019a0001c0001t0014g0020a0001c0001t0033g0021 | 3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.88+12258T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637306 | ||||||
chr16:4637386
|
C | T | 2 | a0001c0001t0009g0075a0001c0001t0009g0076 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.88+12338C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637386 | ||||||
chr16:4637485
|
C | T | 1 | a0001c0001t0021g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.88+12437C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637485 | ||||||
chr16:4637598
|
G | T | 1 | a0001c0001t0037g0082 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.88+12550G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637598 | ||||||
chr16:4637694
|
C | T | 57 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(54): Show | 57 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.88+12646C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637694 | ||||||
chr16:4637770
|
C | T | 1 | a0001c0001t0003g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.89-12595C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637770 | ||||||
chr16:4637956
|
C | G | 6 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0002g0141others(3): Show | 6 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-12409C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637956 | ||||||
chr16:4638016
|
C | T | 2 | a0001c0001t0001g0218a0001c0001t0001g0220 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.89-12349C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638016 | ||||||
chr16:4638057
|
C | A | 6 | a0001c0001t0003g0009a0001c0001t0014g0019a0001c0001t0014g0020others(3): Show | 6 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-12308C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638057 | ||||||
chr16:4638067
|
T | C | 17 | a0001c0001t0002g0105a0001c0001t0003g0009a0001c0001t0005g0036others(14): Show | 17 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.89-12298T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638067 | ||||||
chr16:4638113
|
T | A | 3 | a0001c0001t0002g0202a0001c0001t0006g0158a0001c0001t0006g0309 | 3 | NA18955.hp1 NA19010.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.89-12252T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638113 | ||||||
chr16:4638138
|
C | G | 1 | a0001c0001t0003g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.89-12227C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638138 | ||||||
chr16:4638238
|
G | A | 2 | a0001c0001t0003g0060a0001c0001t0004g0080 | 2 | HG00544.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.89-12127G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638238 | ||||||
chr16:4638257
|
G | A | 9 | a0001c0001t0002g0105a0001c0001t0005g0036a0001c0001t0005g0037others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-12108G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638257 | ||||||
chr16:4638277
|
C | A | 4 | a0001c0001t0001g0193a0001c0001t0001g0201a0001c0001t0001g0231others(1): Show | 4 | HG01106.hp1 HG01243.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-12088C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638277 | ||||||
chr16:4638381
|
C | T | 7 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0001g0191others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-11984C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638381 | ||||||
chr16:4638464
|
C | CA | 13 | a0001c0001t0001g0179a0001c0001t0001g0224a0001c0001t0002g0105others(10): Show | 13 | HG00099.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.89-11890dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4638464 | |||||
chr16:4638476
|
T | A | 75 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.89-11889T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638476 | ||||||
chr16:4638480
|
T | A | 1 | a0001c0001t0003g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.89-11885T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638480 | ||||||
chr16:4638487
|
C | A | 2 | a0001c0001t0003g0013a0001c0001t0022g0014 | 2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.89-11878C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638487 | ||||||
chr16:4638491
|
G | GC | 7 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-11871dupC | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4638491 | |||||
chr16:4638492
|
C | A | 48 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(45): Show | 48 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.89-11873C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638492 | ||||||
chr16:4638517
|
G | T | 1 | a0001c0008t0054g0187 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.89-11848G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638517 | ||||||
chr16:4638550
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0002g0281 | 2 | HG01928.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.89-11815G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638550 | ||||||
chr16:4638674
|
C | A | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-11691C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638674 | ||||||
chr16:4638760
|
C | T | 1 | a0001c0001t0020g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.89-11605C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638760 | ||||||
chr16:4638836
|
C | G | 1 | a0001c0001t0001g0106 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.89-11529C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638836 | ||||||
chr16:4638840
|
C | T | 3 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0003g0051 | 3 | HG01257.hp2 HG01258.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.89-11525C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638840 | ||||||
chr16:4638841
|
C | T | 1 | a0001c0001t0021g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.89-11524C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638841 | ||||||
chr16:4638847
|
T | A | 1 | a0001c0001t0058g0329 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.89-11518T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638847 | ||||||
chr16:4638904
|
G | A | 1 | a0001c0001t0002g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.89-11461G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638904 | ||||||
chr16:4638920
|
A | C | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-11445A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638920 | ||||||
chr16:4638920
|
A | G | 9 | a0001c0001t0002g0105a0001c0001t0005g0036a0001c0001t0005g0037others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-11445A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638920 | ||||||
chr16:4638934
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-11431C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638934 | ||||||
chr16:4638952
|
A | T | 6 | a0001c0001t0003g0009a0001c0001t0014g0019a0001c0001t0014g0020others(3): Show | 6 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-11413A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638952 | ||||||
chr16:4638980
|
T | C | 7 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-11385T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638980 | ||||||
chr16:4639100
|
C | T | 2 | a0001c0001t0002g0105a0001c0001t0019g0010 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.89-11265C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639100 | ||||||
chr16:4639139
|
C | T | 7 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-11226C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639139 | ||||||
chr16:4639191
|
A | T | 6 | a0001c0001t0003g0009a0001c0001t0014g0019a0001c0001t0014g0020others(3): Show | 6 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-11174A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639191 | ||||||
chr16:4639317
|
G | A | 16 | a0001c0001t0002g0105a0001c0001t0003g0009a0001c0001t0005g0036others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-11048G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639317 | ||||||
chr16:4639318
|
T | G | 93 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0122others(90): Show | 93 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.89-11047T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639318 | ||||||
chr16:4639342
|
C | T | 1 | a0001c0001t0007g0148 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.89-11023C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639342 | ||||||
chr16:4639470
|
C | T | 6 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0002g0141others(3): Show | 6 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-10895C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639470 | ||||||
chr16:4639568
|
A | G | 1 | a0001c0001t0034g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.89-10797A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639568 | ||||||
chr16:4639619
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.89-10746G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639619 | ||||||
chr16:4639685
|
C | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0224 | 2 | HG00099.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.89-10680C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639685 | ||||||
chr16:4639696
|
T | A | 17 | a0001c0001t0002g0105a0001c0001t0003g0009a0001c0001t0005g0036others(14): Show | 17 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.89-10669T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639696 | ||||||
chr16:4639812
|
T | C | 6 | a0001c0001t0003g0009a0001c0001t0014g0019a0001c0001t0014g0020others(3): Show | 6 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-10553T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639812 | ||||||
chr16:4640005
|
T | C | 1 | a0001c0001t0009g0090 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.89-10360T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640005 | ||||||
chr16:4640020
|
G | A | 6 | a0001c0001t0003g0009a0001c0001t0014g0019a0001c0001t0014g0020others(3): Show | 6 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-10345G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640020 | ||||||
chr16:4640160
|
T | C | 1 | a0001c0008t0054g0187 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.89-10205T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640160 | ||||||
chr16:4640186
|
G | T | 26 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0217others(23): Show | 26 | HG01070.hp1 HG01099.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.89-10179G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640186 | ||||||
chr16:4640241
|
T | C | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-10124T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640241 | ||||||
chr16:4640262
|
C | T | 1 | a0001c0001t0028g0071 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.89-10103C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640262 | ||||||
chr16:4640362
|
A | C | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-10003A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640362 | ||||||
chr16:4640454
|
C | A | 9 | a0001c0001t0002g0105a0001c0001t0005g0036a0001c0001t0005g0037others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-9911C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640454 | ||||||
chr16:4640455
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.89-9910C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640455 | ||||||
chr16:4640476
|
G | C | 1 | a0001c0001t0021g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.89-9889G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640476 | ||||||
chr16:4640599
|
C | G | 1 | a0001c0001t0001g0188 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.89-9766C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640599 | ||||||
chr16:4640653
|
G | A | 2 | a0001c0002t0003g0004a0001c0002t0004g0003 | 2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.89-9712G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640653 | ||||||
chr16:4640718
|
A | G | 1 | a0001c0001t0005g0044 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.89-9647A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640718 | ||||||
chr16:4640733
|
G | GT | 12 | a0001c0001t0002g0105a0001c0001t0002g0208a0001c0001t0002g0305others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.89-9626dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4640733 | |||||
chr16:4640764
|
C | A | 3 | a0001c0001t0003g0029a0001c0001t0003g0030a0001c0001t0003g0033 | 3 | HG02280.hp2 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.89-9601C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640764 | ||||||
chr16:4640766
|
G | T | 3 | a0001c0001t0003g0013a0001c0001t0020g0012a0001c0001t0022g0014 | 3 | HG02723.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.89-9599G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640766 | ||||||
chr16:4640850
|
G | A | 6 | a0001c0001t0003g0009a0001c0001t0014g0019a0001c0001t0014g0020others(3): Show | 6 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-9515G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640850 | ||||||
chr16:4640991
|
C | T | 3 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0004t0036g0087 | 3 | HG01070.hp1 HG01175.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.89-9374C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640991 | ||||||
chr16:4641021
|
C | T | 1 | a0001c0001t0004g0050 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.89-9344C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641021 | ||||||
chr16:4641052
|
A | G | 1 | a0001c0001t0003g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.89-9313A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641052 | ||||||
chr16:4641116
|
G | A | 2 | a0001c0001t0029g0334a0001c0001t0035g0333 | 2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.89-9249G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641116 | ||||||
chr16:4641145
|
G | C | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-9220G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641145 | ||||||
chr16:4641218
|
G | A | 16 | a0001c0001t0002g0105a0001c0001t0003g0009a0001c0001t0005g0036others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-9147G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641218 | ||||||
chr16:4641224
|
G | C | 16 | a0001c0001t0002g0105a0001c0001t0003g0009a0001c0001t0005g0036others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-9141G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641224 | ||||||
chr16:4641252
|
C | T | 9 | a0001c0001t0002g0105a0001c0001t0005g0036a0001c0001t0005g0037others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-9113C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641252 | ||||||
chr16:4641259
|
C | T | 1 | a0001c0001t0021g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.89-9106C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641259 | ||||||
chr16:4641336
|
A | G | 7 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-9029A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641336 | ||||||
chr16:4641342
|
A | AT | 16 | a0001c0001t0001g0204a0001c0001t0002g0105a0001c0001t0005g0036others(13): Show | 16 | HG00735.hp2 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-9013dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4641342 | |||||
chr16:4641353
|
G | T | 1 | a0001c0001t0001g0222 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.89-9012G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641353 | ||||||
chr16:4641402
|
C | T | 1 | a0001c0001t0021g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.89-8963C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641402 | ||||||
chr16:4641448
|
G | A | 19 | a0001c0001t0003g0009a0001c0001t0005g0036a0001c0001t0005g0037others(16): Show | 19 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.89-8917G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641448 | ||||||
chr16:4641515
|
C | CT | 7 | a0001c0001t0001g0206a0001c0001t0001g0244a0001c0001t0002g0307others(4): Show | 7 | HG00423.hp1 HG01952.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-8831dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4641515 | |||||
chr16:4641515
|
CT | C | 23 | a0001c0001t0001g0134a0001c0001t0001g0178a0001c0001t0001g0284others(20): Show | 23 | HG00323.hp2 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.89-8831delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4641515 | |||||
chr16:4641515
|
CTT | C | 29 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0217others(26): Show | 29 | HG01070.hp1 HG01099.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.89-8832_89-8831del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4641515 | |||||
chr16:4641542
|
C | T | 1 | a0001c0001t0003g0061 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.89-8823C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641542 | ||||||
chr16:4641585
|
C | G | 1 | a0001c0001t0003g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.89-8780C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641585 | ||||||
chr16:4641587
|
C | T | 17 | a0001c0001t0003g0013a0001c0001t0004g0011a0001c0001t0005g0044others(14): Show | 17 | HG01099.hp1 HG01243.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.89-8778C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641587 | ||||||
chr16:4641621
|
T | C | 24 | a0001c0001t0002g0105a0001c0001t0003g0009a0001c0001t0004g0017others(21): Show | 24 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.89-8744T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641621 | ||||||
chr16:4641706
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.89-8659C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641706 | ||||||
chr16:4641809
|
G | A | 4 | a0001c0001t0001g0193a0001c0001t0001g0201a0001c0001t0001g0231others(1): Show | 4 | HG01106.hp1 HG01243.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-8556G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641809 | ||||||
chr16:4641879
|
C | T | 1 | a0001c0001t0002g0259 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.89-8486C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641879 | ||||||
chr16:4641942
|
C | A | 16 | a0001c0001t0003g0009a0001c0001t0003g0098a0001c0001t0004g0011others(13): Show | 16 | HG01099.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.89-8423C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641942 | ||||||
chr16:4642022
|
A | G | 1 | a0001c0001t0002g0314 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.89-8343A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642022 | ||||||
chr16:4642032
|
C | A | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.89-8333C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642032 | ||||||
chr16:4642033
|
C | G | 8 | a0001c0001t0001g0217a0001c0001t0002g0233a0001c0001t0002g0234others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-8332C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642033 | ||||||
chr16:4642033
|
C | T | 2 | a0001c0001t0029g0334a0001c0001t0035g0333 | 2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.89-8332C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642033 | ||||||
chr16:4642060
|
G | A | 18 | a0001c0001t0003g0098a0001c0001t0004g0017a0001c0001t0005g0036others(15): Show | 18 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.89-8305G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642060 | ||||||
chr16:4642068
|
A | G | 1 | a0001c0001t0003g0009 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.89-8297A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642068 | ||||||
chr16:4642090
|
A | G | 122 | a0001c0001t0001g0113a0001c0001t0001g0134a0001c0001t0001g0144others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.89-8275A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642090 | ||||||
chr16:4642112
|
G | A | 43 | a0001c0001t0001g0146a0001c0001t0001g0225a0001c0001t0002g0105others(40): Show | 43 | HG01070.hp1 HG01099.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.89-8253G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642112 | ||||||
chr16:4642128
|
C | CT | 259 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.89-8219dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642128 | |||||
chr16:4642128
|
C | CTT | 30 | a0001c0001t0001g0136a0001c0001t0001g0217a0001c0001t0001g0222others(27): Show | 30 | HG01074.hp2 HG01099.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.89-8220_89-8219dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642128 | |||||
chr16:4642146
|
T | TA | 7 | a0001c0001t0001g0165a0001c0001t0001g0188a0001c0001t0001g0212others(4): Show | 7 | HG00738.hp2 HG01069.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-8213dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642146 | |||||
chr16:4642147
|
A | T | 1 | a0001c0001t0045g0200 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.89-8218A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642147 | ||||||
chr16:4642194
|
G | A | 24 | a0001c0001t0003g0013a0001c0001t0004g0017a0001c0001t0005g0036others(21): Show | 24 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.89-8171G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642194 | ||||||
chr16:4642258
|
G | C | 3 | a0001c0001t0002g0105a0001c0001t0004g0011a0001c0004t0036g0087 | 3 | HG01243.hp1 HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.89-8107G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642258 | ||||||
chr16:4642267
|
A | C | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-8098A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642267 | ||||||
chr16:4642347
|
G | C | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-8018G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642347 | ||||||
chr16:4642374
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.89-7991G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642374 | ||||||
chr16:4642456
|
G | A | 1 | a0001c0001t0016g0070 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.89-7909G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642456 | ||||||
chr16:4642466
|
T | TTG | 30 | a0001c0001t0001g0129a0001c0001t0001g0138a0001c0001t0001g0163others(27): Show | 30 | HG00140.hp1 HG00597.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.89-7865_89-7864dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | |||||
chr16:4642466
|
T | TTGTG | 5 | a0001c0001t0004g0011a0001c0001t0005g0038a0001c0001t0005g0039others(2): Show | 5 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-7867_89-7864dup others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | |||||
chr16:4642466
|
T | TTGTGTG | 11 | a0001c0001t0004g0017a0001c0001t0004g0089a0001c0001t0005g0036others(8): Show | 11 | HG01891.hp2 HG01975.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.89-7869_89-7864dup others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | |||||
chr16:4642466
|
T | TTGTGTGT others(1): Show |
7 | a0001c0001t0005g0032a0001c0001t0005g0044a0001c0001t0009g0093others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-7871_89-7864dup others(8): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | |||||
chr16:4642466
|
T | TTGTGTGT others(3): Show |
10 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(7): Show | 10 | HG02015.hp1 HG02083.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-7873_89-7864dup others(10): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | |||||
chr16:4642466
|
T | TTGTGTGT others(5): Show |
6 | a0001c0001t0005g0084a0001c0001t0020g0012a0001c0001t0023g0006others(3): Show | 6 | HG01099.hp1 HG02922.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-7875_89-7864dup others(12): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | |||||
chr16:4642466
|
T | TTGTGTGT others(7): Show |
2 | a0001c0001t0014g0019a0001c0001t0014g0020 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.89-7877_89-7864dup others(14): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | |||||
chr16:4642466
|
T | TTGTGTGT others(9): Show |
2 | a0001c0001t0033g0021a0001c0002t0005g0001 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.89-7879_89-7864dup others(16): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | |||||
chr16:4642466
|
T | TTGTGTGT others(11): Show |
1 | a0001c0004t0036g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-7881_89-7864dup others(18): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | |||||
chr16:4642466
|
T | TTGTGTGT others(15): Show |
1 | a0001c0001t0003g0009 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.89-7885_89-7864dup others(22): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | |||||
chr16:4642466
|
T | TTGTGTGT others(19): Show |
2 | a0001c0001t0029g0334a0001c0001t0035g0333 | 2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.89-7889_89-7864dup others(26): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | |||||
chr16:4642466
|
TTG | T | 9 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0202others(6): Show | 9 | HG01175.hp2 HG01361.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.89-7865_89-7864del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | |||||
chr16:4642466
|
TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.89-7873_89-7864del others(10): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | |||||
chr16:4642466
|
TTGTGTGT others(11): Show |
T | 1 | a0001c0001t0003g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.89-7881_89-7864del others(18): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | |||||
chr16:4642526
|
C | G | 1 | a0001c0004t0036g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-7839C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642526 | ||||||
chr16:4642556
|
C | T | 4 | a0001c0001t0004g0011a0001c0001t0014g0019a0001c0001t0014g0020others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-7809C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642556 | ||||||
chr16:4642571
|
G | A | 1 | a0001c0001t0059g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.89-7794G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642571 | ||||||
chr16:4642614
|
G | A | 20 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0004g0017others(17): Show | 20 | HG01099.hp1 HG01891.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.89-7751G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642614 | ||||||
chr16:4642690
|
C | G | 1 | a0001c0001t0005g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.89-7675C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642690 | ||||||
chr16:4642691
|
G | T | 6 | a0001c0001t0004g0011a0001c0001t0014g0019a0001c0001t0014g0020others(3): Show | 6 | HG01099.hp1 HG01243.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-7674G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642691 | ||||||
chr16:4642744
|
G | A | 3 | a0001c0001t0023g0006a0001c0001t0029g0334a0001c0001t0035g0333 | 3 | HG02896.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.89-7621G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642744 | ||||||
chr16:4642788
|
A | AT | 7 | a0001c0001t0001g0118a0001c0001t0001g0137a0001c0001t0001g0249others(4): Show | 7 | HG00544.hp2 HG02809.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-7561dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642788 | |||||
chr16:4642788
|
AT | A | 14 | a0001c0001t0001g0265a0001c0001t0002g0214a0001c0001t0003g0098others(11): Show | 14 | HG00673.hp1 HG01099.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.89-7561delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642788 | |||||
chr16:4642788
|
ATT | A | 6 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-7562_89-7561del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642788 | |||||
chr16:4642934
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.89-7431G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642934 | ||||||
chr16:4642980
|
C | CAG | 168 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0217others(165): Show | 168 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.89-7384_89-7383dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642980 | |||||
chr16:4643023
|
T | C | 3 | a0001c0001t0001g0261a0001c0001t0001g0266a0001c0001t0001g0267 | 3 | HG00673.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.89-7342T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643023 | ||||||
chr16:4643049
|
A | C | 1 | a0001c0001t0013g0288 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.89-7316A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643049 | ||||||
chr16:4643168
|
C | A | 4 | a0001c0001t0004g0011a0001c0001t0014g0019a0001c0001t0014g0020others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-7197C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643168 | ||||||
chr16:4643190
|
G | T | 27 | a0001c0001t0002g0105a0001c0001t0003g0009a0001c0001t0003g0013others(24): Show | 27 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(24): Show |
intron_variant | MODIFIER | c.89-7175G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643190 | ||||||
chr16:4643231
|
A | G | 1 | a0001c0001t0002g0208 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.89-7134A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643231 | ||||||
chr16:4643241
|
C | T | 6 | a0001c0001t0032g0002a0001c0002t0003g0004a0001c0002t0003g0005others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-7124C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643241 | ||||||
chr16:4643301
|
G | A | 2 | a0001c0001t0002g0202a0001c0001t0002g0253 | 2 | NA18955.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.89-7064G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643301 | ||||||
chr16:4643344
|
C | G | 1 | a0001c0004t0036g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-7021C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643344 | ||||||
chr16:4643391
|
C | T | 2 | a0001c0001t0004g0017a0001c0003t0038g0018 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.89-6974C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643391 | ||||||
chr16:4643403
|
A | AT | 34 | a0001c0001t0001g0118a0001c0001t0001g0163a0001c0001t0001g0175others(31): Show | 34 | HG00735.hp2 HG01070.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.89-6941dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4643403 | |||||
chr16:4643403
|
A | ATT | 6 | a0001c0001t0002g0319a0001c0001t0004g0017a0001c0002t0003g0004others(3): Show | 6 | HG01099.hp1 HG03139.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-6942_89-6941dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4643403 | |||||
chr16:4643403
|
AT | A | 28 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0140others(25): Show | 28 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.89-6941delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4643403 | |||||
chr16:4643456
|
G | T | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-6909G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643456 | ||||||
chr16:4643594
|
C | A | 311 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.89-6771C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643594 | ||||||
chr16:4643594
|
C | G | 9 | a0001c0001t0002g0105a0001c0001t0002g0260a0001c0001t0003g0009others(6): Show | 9 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-6771C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643594 | ||||||
chr16:4643595
|
A | G | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-6770A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643595 | ||||||
chr16:4643647
|
C | T | 6 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-6718C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643647 | ||||||
chr16:4643649
|
C | G | 1 | a0001c0001t0025g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.89-6716C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643649 | ||||||
chr16:4643657
|
T | C | 42 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(39): Show | 42 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.89-6708T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643657 | ||||||
chr16:4643711
|
A | G | 8 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0171others(5): Show | 8 | HG00544.hp1 HG00673.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-6654A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643711 | ||||||
chr16:4643802
|
A | G | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-6563A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643802 | ||||||
chr16:4643841
|
A | T | 42 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(39): Show | 42 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.89-6524A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643841 | ||||||
chr16:4643868
|
T | C | 1 | a0001c0001t0006g0252 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.89-6497T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643868 | ||||||
chr16:4643973
|
TG | T | 41 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(38): Show | 41 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.89-6391delG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643973 | ||||||
chr16:4643974
|
G | T | 1 | a0001c0004t0036g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-6391G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643974 | ||||||
chr16:4643986
|
T | G | 7 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(4): Show | 7 | HG00597.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-6379T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643986 | ||||||
chr16:4644004
|
G | A | 1 | a0001c0001t0002g0307 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.89-6361G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644004 | ||||||
chr16:4644124
|
T | C | 1 | a0001c0001t0001g0265 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.89-6241T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644124 | ||||||
chr16:4644154
|
G | T | 23 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(20): Show | 23 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.89-6211G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644154 | ||||||
chr16:4644227
|
A | C | 1 | a0001c0002t0003g0005 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.89-6138A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644227 | ||||||
chr16:4644276
|
G | T | 10 | a0001c0001t0001g0327a0001c0001t0002g0198a0001c0001t0002g0216others(7): Show | 10 | HG00597.hp1 HG02027.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.89-6089G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644276 | ||||||
chr16:4644277
|
C | T | 15 | a0001c0001t0003g0013a0001c0001t0005g0036a0001c0001t0005g0037others(12): Show | 15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.89-6088C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644277 | ||||||
chr16:4644305
|
G | GT | 33 | a0001c0001t0001g0122a0001c0001t0001g0128a0001c0001t0001g0204others(30): Show | 33 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.89-6039dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4644305 | |||||
chr16:4644305
|
GT | G | 16 | a0001c0001t0001g0228a0001c0001t0002g0102a0001c0001t0003g0051others(13): Show | 16 | HG01884.hp1 HG02056.hp2 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-6039delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4644305 | |||||
chr16:4644310
|
T | G | 1 | a0001c0001t0015g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.89-6055T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644310 | ||||||
chr16:4644312
|
T | G | 1 | a0001c0001t0060g0238 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.89-6053T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644312 | ||||||
chr16:4644341
|
C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG02723.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.89-6024C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644341 | ||||||
chr16:4644373
|
C | T | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-5992C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644373 | ||||||
chr16:4644386
|
C | T | 1 | a0001c0001t0007g0159 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.89-5979C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644386 | ||||||
chr16:4644387
|
G | C | 42 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(39): Show | 42 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.89-5978G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644387 | ||||||
chr16:4644413
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.89-5952C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644413 | ||||||
chr16:4644508
|
C | G | 4 | a0001c0001t0004g0089a0001c0001t0005g0032a0001c0001t0005g0091others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-5857C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644508 | ||||||
chr16:4644611
|
C | G | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-5754C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644611 | ||||||
chr16:4644703
|
C | G | 30 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(27): Show | 30 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.89-5662C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644703 | ||||||
chr16:4644827
|
A | G | 2 | a0001c0001t0002g0142a0001c0001t0062g0143 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.89-5538A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644827 | ||||||
chr16:4644875
|
T | A | 1 | a0001c0001t0012g0180 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.89-5490T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644875 | ||||||
chr16:4644915
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.89-5450C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644915 | ||||||
chr16:4644932
|
A | T | 1 | a0001c0001t0003g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.89-5433A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644932 | ||||||
chr16:4644990
|
T | C | 44 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(41): Show | 44 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.89-5375T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644990 | ||||||
chr16:4645019
|
A | C | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.89-5346A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645019 | ||||||
chr16:4645030
|
A | T | 1 | a0001c0004t0036g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-5335A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645030 | ||||||
chr16:4645088
|
T | C | 2 | a0001c0001t0001g0228a0001c0001t0063g0296 | 2 | HG02056.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.89-5277T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645088 | ||||||
chr16:4645104
|
T | C | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.89-5261T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645104 | ||||||
chr16:4645115
|
G | A | 2 | a0001c0001t0013g0185a0001c0001t0013g0186 | 2 | HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.89-5250G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645115 | ||||||
chr16:4645168
|
G | T | 1 | a0001c0001t0010g0121 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.89-5197G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645168 | ||||||
chr16:4645183
|
CAG | C | 19 | a0001c0001t0003g0013a0001c0001t0005g0036a0001c0001t0005g0037others(16): Show | 19 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.89-5181_89-5180del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645183 | ||||||
chr16:4645222
|
G | A | 15 | a0001c0001t0003g0013a0001c0001t0005g0036a0001c0001t0005g0037others(12): Show | 15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.89-5143G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645222 | ||||||
chr16:4645238
|
C | T | 2 | a0001c0001t0029g0334a0001c0001t0035g0333 | 2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.89-5127C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645238 | ||||||
chr16:4645407
|
G | A | 12 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(9): Show | 12 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.89-4958G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645407 | ||||||
chr16:4645519
|
C | T | 1 | a0001c0001t0002g0319 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.89-4846C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645519 | ||||||
chr16:4645534
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0146 | 2 | HG01070.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.89-4831C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645534 | ||||||
chr16:4645589
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.89-4776T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645589 | ||||||
chr16:4645652
|
G | A | 1 | a0001c0001t0016g0070 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.89-4713G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645652 | ||||||
chr16:4645678
|
T | C | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-4687T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645678 | ||||||
chr16:4645690
|
G | A | 15 | a0001c0001t0003g0013a0001c0001t0005g0036a0001c0001t0005g0037others(12): Show | 15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.89-4675G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645690 | ||||||
chr16:4645699
|
G | C | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-4666G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645699 | ||||||
chr16:4645705
|
C | T | 1 | a0001c0001t0002g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.89-4660C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645705 | ||||||
chr16:4645829
|
G | T | 8 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0171others(5): Show | 8 | HG00544.hp1 HG00673.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-4536G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645829 | ||||||
chr16:4645831
|
G | A | 3 | a0001c0001t0002g0233a0001c0001t0002g0234a0001c0001t0002g0235 | 3 | HG02055.hp2 HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.89-4534G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645831 | ||||||
chr16:4645889
|
A | G | 1 | a0001c0001t0031g0046 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.89-4476A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645889 | ||||||
chr16:4645925
|
A | G | 2 | a0001c0001t0002g0260a0001c0001t0003g0098 | 2 | NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.89-4440A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645925 | ||||||
chr16:4645948
|
A | G | 6 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-4417A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645948 | ||||||
chr16:4645961
|
T | C | 38 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(35): Show | 38 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.89-4404T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645961 | ||||||
chr16:4646009
|
C | T | 1 | a0001c0001t0006g0157 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.89-4356C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646009 | ||||||
chr16:4646076
|
C | T | 1 | a0001c0001t0012g0170 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.89-4289C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646076 | ||||||
chr16:4646107
|
C | CG | 16 | a0001c0001t0002g0202a0001c0001t0003g0013a0001c0001t0005g0036others(13): Show | 16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-4252dupG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4646107 | |||||
chr16:4646198
|
A | G | 1 | a0002c0009t0001g0248 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.89-4167A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646198 | ||||||
chr16:4646209
|
T | C | 2 | a0001c0001t0006g0132a0001c0001t0006g0257 | 2 | HG01192.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.89-4156T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646209 | ||||||
chr16:4646223
|
C | A | 43 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(40): Show | 43 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.89-4142C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646223 | ||||||
chr16:4646422
|
C | CA | 20 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(17): Show | 20 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.89-3930dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4646422 | |||||
chr16:4646422
|
C | CAAA | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-3932_89-3930dup others(3): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4646422 | |||||
chr16:4646476
|
A | G | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-3889A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646476 | ||||||
chr16:4646566
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.89-3799T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646566 | ||||||
chr16:4646653
|
T | C | 41 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(38): Show | 41 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.89-3712T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646653 | ||||||
chr16:4646658
|
A | G | 1 | a0001c0004t0036g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-3707A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646658 | ||||||
chr16:4646771
|
C | G | 6 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-3594C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646771 | ||||||
chr16:4646803
|
G | A | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-3562G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646803 | ||||||
chr16:4646973
|
C | T | 4 | a0001c0001t0004g0011a0001c0001t0014g0019a0001c0001t0014g0020others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-3392C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646973 | ||||||
chr16:4647004
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.89-3361C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647004 | ||||||
chr16:4647050
|
G | A | 1 | a0001c0001t0007g0148 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.89-3315G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647050 | ||||||
chr16:4647087
|
A | C | 1 | a0001c0001t0004g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.89-3278A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647087 | ||||||
chr16:4647100
|
C | T | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-3265C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647100 | ||||||
chr16:4647188
|
A | C | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02015.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.89-3177A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647188 | ||||||
chr16:4647212
|
C | T | 1 | a0001c0001t0005g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.89-3153C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647212 | ||||||
chr16:4647255
|
A | G | 15 | a0001c0001t0003g0013a0001c0001t0005g0036a0001c0001t0005g0037others(12): Show | 15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.89-3110A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647255 | ||||||
chr16:4647258
|
A | T | 6 | a0001c0001t0032g0002a0001c0002t0003g0004a0001c0002t0003g0005others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-3107A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647258 | ||||||
chr16:4647370
|
T | C | 11 | a0001c0001t0002g0105a0001c0001t0002g0260a0001c0001t0003g0009others(8): Show | 11 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.89-2995T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647370 | ||||||
chr16:4647377
|
CTT | C | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-2986_89-2985del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4647377 | |||||
chr16:4647511
|
C | T | 2 | a0001c0001t0003g0013a0001c0001t0022g0014 | 2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.89-2854C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647511 | ||||||
chr16:4647516
|
G | T | 1 | a0001c0001t0001g0264 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.89-2849G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647516 | ||||||
chr16:4647672
|
C | G | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-2693C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647672 | ||||||
chr16:4647675
|
T | G | 3 | a0001c0001t0001g0136a0001c0001t0003g0047a0001c0001t0003g0048 | 3 | NA18978.hp1 NA18978.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.89-2690T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647675 | ||||||
chr16:4647793
|
G | A | 1 | a0001c0002t0003g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89-2572G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647793 | ||||||
chr16:4647829
|
C | A | 2 | a0001c0002t0003g0004a0001c0002t0004g0003 | 2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.89-2536C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647829 | ||||||
chr16:4648174
|
A | G | 6 | a0001c0001t0032g0002a0001c0002t0003g0004a0001c0002t0003g0005others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-2191A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648174 | ||||||
chr16:4648191
|
T | C | 14 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(11): Show | 14 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.89-2174T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648191 | ||||||
chr16:4648258
|
C | G | 9 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.89-2107C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648258 | ||||||
chr16:4648273
|
A | G | 6 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-2092A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648273 | ||||||
chr16:4648276
|
C | T | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.89-2089C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648276 | ||||||
chr16:4648294
|
C | G | 6 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-2071C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648294 | ||||||
chr16:4648296
|
C | T | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.89-2069C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648296 | ||||||
chr16:4648304
|
CGCGGGCT others(423): Show |
C | 15 | a0001c0001t0003g0013a0001c0001t0005g0036a0001c0001t0005g0037others(12): Show | 15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.89-2059_89-1630del | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648304 | |||||
chr16:4648305
|
GCGGGCTC others(208): Show |
G | 6 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-2059_89-1845del | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648305 | ||||||
chr16:4648306
|
C | G | 19 | a0001c0001t0002g0105a0001c0001t0002g0260a0001c0001t0003g0009others(16): Show | 19 | HG01099.hp1 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.89-2059C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648306 | ||||||
chr16:4648339
|
T | C | 17 | a0001c0001t0001g0239a0001c0001t0001g0244a0001c0001t0002g0237others(14): Show | 17 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.89-2026T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648339 | ||||||
chr16:4648345
|
A | G | 4 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0004g0003others(1): Show | 4 | HG01099.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-2020A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648345 | ||||||
chr16:4648381
|
A | G | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1984A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648381 | ||||||
chr16:4648402
|
G | GTCCTCCT others(29): Show |
1 | a0001c0003t0038g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.89-1953_89-1952ins others(36): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648402 | |||||
chr16:4648413
|
G | C | 1 | a0001c0001t0004g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.89-1952G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648413 | ||||||
chr16:4648447
|
T | C | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1918T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648447 | ||||||
chr16:4648449
|
G | C | 1 | a0001c0003t0038g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.89-1916G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648449 | ||||||
chr16:4648453
|
A | G | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1912A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648453 | ||||||
chr16:4648454
|
C | G | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-1911C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648454 | ||||||
chr16:4648471
|
T | C | 24 | a0001c0001t0001g0172a0001c0001t0001g0244a0001c0001t0002g0105others(21): Show | 24 | HG01099.hp1 HG01243.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.89-1894T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648471 | ||||||
chr16:4648474
|
C | G | 2 | a0001c0001t0001g0172a0001c0001t0032g0002 | 2 | HG01884.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.89-1891C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648474 | ||||||
chr16:4648475
|
T | G | 1 | a0001c0001t0001g0172 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.89-1890T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648475 | ||||||
chr16:4648476
|
C | G | 1 | a0001c0001t0001g0172 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.89-1889C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648476 | ||||||
chr16:4648485
|
G | C | 1 | a0001c0001t0004g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.89-1880G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648485 | ||||||
chr16:4648509
|
G | GCTCCTCC others(493): Show |
1 | a0001c0004t0036g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-1856_89-1855ins others(500): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648509 | ||||||
chr16:4648509
|
G | GCTCCTCC others(387): Show |
1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-1856_89-1855ins others(394): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648509 | ||||||
chr16:4648509
|
G | GCTCCTCC others(315): Show |
1 | a0001c0001t0004g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.89-1856_89-1855ins others(322): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648509 | ||||||
chr16:4648510
|
G | C | 6 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0004g0003others(3): Show | 6 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1855G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648510 | ||||||
chr16:4648511
|
G | T | 5 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0004g0003others(2): Show | 5 | HG01099.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1854G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648511 | ||||||
chr16:4648512
|
G | C | 5 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0004g0003others(2): Show | 5 | HG01099.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1853G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648512 | ||||||
chr16:4648512
|
GCTCCTCC others(64): Show |
G | 2 | a0001c0001t0002g0308a0001c0001t0047g0283 | 2 | HG00408.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.89-1806_89-1736del others(71): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648512 | |||||
chr16:4648520
|
C | CG | 5 | a0001c0001t0032g0002a0001c0002t0003g0005a0001c0002t0004g0003others(2): Show | 5 | HG01099.hp1 HG01884.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1841dupG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648520 | |||||
chr16:4648524
|
G | GGCTCTTC others(30): Show |
1 | a0001c0002t0003g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89-1841_89-1840ins others(37): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648524 | ||||||
chr16:4648533
|
G | A | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-1832G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648533 | ||||||
chr16:4648533
|
G | T | 2 | a0001c0001t0002g0260a0001c0001t0003g0098 | 2 | NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.89-1832G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648533 | ||||||
chr16:4648545
|
G | C | 5 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0004g0003others(2): Show | 5 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1820G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648545 | ||||||
chr16:4648549
|
T | A | 11 | a0001c0001t0002g0105a0001c0001t0002g0260a0001c0001t0003g0009others(8): Show | 11 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.89-1816T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648549 | ||||||
chr16:4648556
|
G | GGGGGCTC others(135): Show |
2 | a0001c0001t0002g0260a0001c0001t0003g0098 | 2 | NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.89-1740_89-1739ins others(142): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648556 | |||||
chr16:4648560
|
G | A | 3 | a0001c0002t0003g0005a0001c0002t0004g0003a0001c0002t0005g0001 | 3 | HG01099.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.89-1805G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648560 | ||||||
chr16:4648581
|
G | C | 6 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0005others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-1784G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648581 | ||||||
chr16:4648591
|
C | CG | 6 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0004g0003others(3): Show | 6 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1770dupG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648591 | |||||
chr16:4648595
|
G | GA | 6 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1770_89-1769ins others(1): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648595 | ||||||
chr16:4648616
|
G | C | 10 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-1749G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648616 | ||||||
chr16:4648623
|
T | TCTCCGGG others(30): Show |
1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-1741_89-1740ins others(37): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648623 | |||||
chr16:4648624
|
C | CT | 7 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-1741_89-1740ins others(1): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648624 | ||||||
chr16:4648626
|
C | CG | 6 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0004g0003others(3): Show | 6 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1736dupG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648626 | |||||
chr16:4648626
|
C | G | 7 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-1739C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648626 | ||||||
chr16:4648626
|
C | T | 4 | a0001c0001t0004g0011a0001c0001t0014g0019a0001c0001t0014g0020others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-1739C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648626 | ||||||
chr16:4648630
|
A | G | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1735A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648630 | ||||||
chr16:4648651
|
C | G | 1 | a0001c0001t0009g0076 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.89-1714C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648651 | ||||||
chr16:4648660
|
C | T | 6 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1705C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648660 | ||||||
chr16:4648666
|
A | G | 14 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0004g0017others(11): Show | 14 | HG00280.hp2 HG01099.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.89-1699A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648666 | ||||||
chr16:4648666
|
ACTCTTCC others(170): Show |
A | 6 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1678_89-1502del | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648666 | |||||
chr16:4648687
|
G | C | 5 | a0001c0001t0004g0017a0001c0002t0003g0005a0001c0002t0004g0003others(2): Show | 5 | HG01099.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1678G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648687 | ||||||
chr16:4648696
|
C | T | 1 | a0001c0002t0003g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89-1669C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648696 | ||||||
chr16:4648698
|
G | C | 1 | a0001c0002t0003g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89-1667G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648698 | ||||||
chr16:4648701
|
G | T | 1 | a0001c0001t0002g0310 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.89-1664G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648701 | ||||||
chr16:4648723
|
C | G | 3 | a0001c0002t0003g0005a0001c0002t0004g0003a0001c0002t0005g0001 | 3 | HG01099.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.89-1642C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648723 | ||||||
chr16:4648728
|
C | T | 1 | a0001c0001t0048g0177 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.89-1637C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648728 | ||||||
chr16:4648732
|
T | C | 5 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(2): Show | 5 | HG01884.hp1 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-1633T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648732 | ||||||
chr16:4648734
|
G | C | 3 | a0001c0002t0003g0005a0001c0002t0004g0003a0001c0002t0005g0001 | 3 | HG01099.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.89-1631G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648734 | ||||||
chr16:4648738
|
A | G | 24 | a0001c0001t0003g0013a0001c0001t0004g0017a0001c0001t0005g0036others(21): Show | 24 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.89-1627A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648738 | ||||||
chr16:4648738
|
ACTCTTCC others(28): Show |
A | 1 | a0001c0001t0001g0134 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.89-1606_89-1572del others(35): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648738 | |||||
chr16:4648738
|
ACTCTTCC others(98): Show |
A | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.89-1597_89-1493del | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648738 | |||||
chr16:4648741
|
C | G | 1 | a0001c0002t0003g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89-1624C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648741 | ||||||
chr16:4648756
|
C | CGGCTCCT others(1035): Show |
1 | a0001c0004t0036g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-1592_89-1591ins others(1042): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648756 | |||||
chr16:4648759
|
C | G | 15 | a0001c0001t0003g0013a0001c0001t0005g0036a0001c0001t0005g0037others(12): Show | 15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.89-1606C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648759 | ||||||
chr16:4648769
|
C | CGGGGGCT others(916): Show |
1 | a0001c0002t0003g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89-1592_89-1591ins others(923): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648769 | |||||
chr16:4648769
|
C | CGGGGGCT others(485): Show |
1 | a0001c0001t0004g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.89-1592_89-1591ins others(492): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648769 | |||||
chr16:4648769
|
C | CGGGGGCT others(952): Show |
2 | a0001c0002t0003g0005a0001c0002t0004g0003 | 2 | HG01099.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.89-1592_89-1591ins others(959): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648769 | |||||
chr16:4648769
|
C | CGGGGGCT others(952): Show |
1 | a0001c0002t0005g0001 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.89-1592_89-1591ins others(959): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648769 | |||||
chr16:4648781
|
C | T | 1 | a0001c0001t0003g0056 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.89-1584C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648781 | ||||||
chr16:4648794
|
G | C | 9 | a0001c0001t0002g0260a0001c0001t0003g0098a0001c0001t0004g0017others(6): Show | 9 | HG01099.hp1 HG01884.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.89-1571G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648794 | ||||||
chr16:4648804
|
C | CG | 5 | a0001c0001t0004g0017a0001c0002t0003g0004a0001c0002t0003g0005others(2): Show | 5 | HG01099.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1557dupG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648804 | |||||
chr16:4648804
|
C | CGGGGGCT others(881): Show |
1 | a0001c0003t0038g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.89-1557_89-1556ins others(888): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648804 | |||||
chr16:4648808
|
G | GA | 3 | a0001c0001t0002g0260a0001c0001t0003g0098a0001c0004t0036g0087 | 3 | HG02809.hp2 NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.89-1557_89-1556ins others(1): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648808 | ||||||
chr16:4648829
|
G | C | 6 | a0001c0001t0004g0017a0001c0002t0003g0004a0001c0002t0003g0005others(3): Show | 6 | HG01099.hp1 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1536G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648829 | ||||||
chr16:4648838
|
C | T | 2 | a0001c0001t0002g0260a0001c0001t0003g0098 | 2 | NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.89-1527C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648838 | ||||||
chr16:4648839
|
C | CG | 6 | a0001c0001t0004g0017a0001c0002t0003g0004a0001c0002t0003g0005others(3): Show | 6 | HG01099.hp1 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1522dupG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | |||||
chr16:4648839
|
C | CGGGACTC others(529): Show |
1 | a0001c0001t0006g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.89-1523_89-1522ins others(536): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | |||||
chr16:4648839
|
C | CGGGACTC others(529): Show |
2 | a0001c0001t0002g0105a0001c0001t0019g0010 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.89-1523_89-1522ins others(536): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | |||||
chr16:4648839
|
C | CGGGACTC others(529): Show |
1 | a0001c0001t0008g0035 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.89-1523_89-1522ins others(536): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | |||||
chr16:4648839
|
C | CGGGACTC others(423): Show |
1 | a0001c0001t0003g0009 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.89-1523_89-1522ins others(430): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | |||||
chr16:4648839
|
C | CGGGACTC others(529): Show |
1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-1523_89-1522ins others(536): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | |||||
chr16:4648839
|
C | CGGGACTC others(529): Show |
3 | a0001c0001t0014g0019a0001c0001t0014g0020a0001c0001t0033g0021 | 3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.89-1523_89-1522ins others(536): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | |||||
chr16:4648839
|
C | CGGGGACT others(341): Show |
1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-1522_89-1521ins others(348): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | |||||
chr16:4648839
|
C | CGGGGGCT others(521): Show |
1 | a0001c0004t0036g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-1522_89-1521ins others(528): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | |||||
chr16:4648843
|
G | A | 9 | a0001c0001t0002g0105a0001c0001t0003g0009a0001c0001t0004g0011others(6): Show | 9 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-1522G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648843 | ||||||
chr16:4648843
|
G | GACTCTTC others(351): Show |
2 | a0001c0001t0002g0260a0001c0001t0003g0098 | 2 | NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.89-1522_89-1521ins others(358): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648843 | ||||||
chr16:4648843
|
G | GCTCTTCC others(29): Show |
3 | a0001c0001t0023g0006a0001c0001t0029g0334a0001c0001t0035g0333 | 3 | HG02896.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.89-1465_89-1430dup others(36): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648843 | |||||
chr16:4648864
|
C | G | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1501C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648864 | ||||||
chr16:4648873
|
T | C | 25 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(22): Show | 25 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.89-1492T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648873 | ||||||
chr16:4648879
|
A | G | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1486A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648879 | ||||||
chr16:4648900
|
C | G | 6 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0013g0131others(3): Show | 6 | HG00280.hp2 HG02602.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-1465C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648900 | ||||||
chr16:4648909
|
T | C | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1456T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648909 | ||||||
chr16:4648915
|
A | G | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1450A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648915 | ||||||
chr16:4649149
|
T | G | 2 | a0001c0001t0006g0219a0001c0001t0037g0082 | 2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.89-1216T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649149 | ||||||
chr16:4649152
|
C | T | 2 | a0001c0001t0004g0017a0001c0003t0038g0018 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.89-1213C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649152 | ||||||
chr16:4649153
|
G | A | 1 | a0001c0001t0002g0104 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.89-1212G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649153 | ||||||
chr16:4649163
|
G | A | 1 | a0001c0001t0006g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.89-1202G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649163 | ||||||
chr16:4649167
|
G | T | 1 | a0001c0001t0003g0015 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.89-1198G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649167 | ||||||
chr16:4649291
|
A | C | 1 | a0001c0001t0006g0257 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.89-1074A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649291 | ||||||
chr16:4649318
|
A | G | 2 | a0001c0001t0001g0204a0001c0001t0001g0212 | 2 | HG00735.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.89-1047A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649318 | ||||||
chr16:4649378
|
A | C | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-987A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649378 | ||||||
chr16:4649389
|
C | T | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-976C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649389 | ||||||
chr16:4649412
|
C | T | 4 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0004g0003others(1): Show | 4 | HG01099.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-953C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649412 | ||||||
chr16:4649421
|
C | T | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-944C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649421 | ||||||
chr16:4649507
|
G | C | 48 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0001g0144others(45): Show | 48 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.89-858G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649507 | ||||||
chr16:4649554
|
C | T | 1 | a0003c0007t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.89-811C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649554 | ||||||
chr16:4649593
|
T | A | 15 | a0001c0001t0003g0013a0001c0001t0005g0036a0001c0001t0005g0037others(12): Show | 15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.89-772T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649593 | ||||||
chr16:4649657
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.89-708C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649657 | ||||||
chr16:4649761
|
T | C | 2 | a0001c0001t0002g0236a0001c0001t0007g0312 | 2 | HG02165.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.89-604T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649761 | ||||||
chr16:4649770
|
G | T | 2 | a0001c0001t0011g0291a0001c0001t0055g0278 | 2 | HG02071.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.89-595G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649770 | ||||||
chr16:4649902
|
A | G | 51 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0001g0144others(48): Show | 51 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(48): Show |
intron_variant | MODIFIER | c.89-463A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649902 | ||||||
chr16:4649905
|
C | T | 1 | a0001c0001t0010g0121 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.89-460C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649905 | ||||||
chr16:4649918
|
G | C | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-447G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649918 | ||||||
chr16:4649955
|
G | A | 1 | a0001c0001t0003g0061 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.89-410G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649955 | ||||||
chr16:4649967
|
C | T | 1 | a0001c0001t0007g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.89-398C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649967 | ||||||
chr16:4650006
|
C | G | 1 | a0001c0001t0019g0010 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.89-359C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650006 | ||||||
chr16:4650008
|
A | G | 3 | a0001c0001t0014g0019a0001c0001t0014g0020a0001c0001t0033g0021 | 3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.89-357A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650008 | ||||||
chr16:4650031
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.89-334C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650031 | ||||||
chr16:4650055
|
A | C | 30 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0001g0144others(27): Show | 30 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.89-310A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650055 | ||||||
chr16:4650065
|
GGCTGAGG others(11): Show |
G | 4 | a0001c0001t0002g0174a0001c0001t0005g0088a0001c0001t0042g0189others(1): Show | 4 | HG02630.hp2 HG02647.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-299_89-282delGC others(16): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650065 | ||||||
chr16:4650092
|
C | T | 11 | a0001c0001t0002g0105a0001c0001t0004g0017a0001c0001t0006g0154others(8): Show | 11 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.89-273C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650092 | ||||||
chr16:4650131
|
C | T | 6 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-234C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650131 | ||||||
chr16:4650179
|
G | A | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.89-186G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650179 | ||||||
chr16:4650195
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.89-170C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650195 | ||||||
chr16:4650317
|
C | CA | 16 | a0001c0001t0001g0106a0001c0001t0001g0138a0001c0001t0001g0155others(13): Show | 16 | HG00558.hp2 HG01109.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-30dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4650317 | |||||
chr16:4650317
|
CAAA | C | 7 | a0001c0001t0004g0017a0001c0002t0003g0004a0001c0002t0003g0005others(4): Show | 7 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-32_89-30delAAA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4650317 | |||||
chr16:4650524
|
G | A | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+41G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4650524 | ||||||
chr16:4650540
|
A | C | 2 | a0001c0001t0002g0142a0001c0001t0062g0143 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.207+57A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4650540 | ||||||
chr16:4650609
|
C | T | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.207+126C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4650609 | ||||||
chr16:4650624
|
G | T | 2 | a0001c0001t0003g0078a0001c0001t0003g0079 | 2 | NA18977.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.207+141G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4650624 | ||||||
chr16:4650660
|
T | C | 5 | a0001c0001t0004g0011a0001c0001t0006g0219a0001c0001t0014g0019others(2): Show | 5 | HG01243.hp1 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+177T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4650660 | ||||||
chr16:4650674
|
C | G | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.207+191C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4650674 | ||||||
chr16:4650878
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.207+395G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4650878 | ||||||
chr16:4650904
|
T | G | 8 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0002g0202others(5): Show | 8 | HG00408.hp2 HG00621.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+421T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4650904 | ||||||
chr16:4651057
|
C | T | 1 | a0001c0004t0036g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.207+574C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651057 | ||||||
chr16:4651072
|
A | G | 48 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0001g0144others(45): Show | 48 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.207+589A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651072 | ||||||
chr16:4651110
|
G | GA | 21 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(18): Show | 21 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.207+641dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr16 | 4651110 | |||||
chr16:4651110
|
GA | G | 12 | a0001c0001t0001g0239a0001c0001t0002g0305a0001c0001t0003g0065others(9): Show | 12 | HG00140.hp1 HG00323.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+641delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr16 | 4651110 | |||||
chr16:4651127
|
A | T | 2 | a0001c0001t0029g0334a0001c0001t0035g0333 | 2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.207+644A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651127 | ||||||
chr16:4651147
|
A | C | 6 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+664A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651147 | ||||||
chr16:4651247
|
C | T | 14 | a0001c0001t0001g0122a0001c0001t0001g0222a0001c0001t0001g0245others(11): Show | 14 | HG00621.hp2 HG02015.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.208-716C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651247 | ||||||
chr16:4651248
|
G | A | 1 | a0001c0001t0006g0252 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.208-715G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651248 | ||||||
chr16:4651264
|
C | CTGTT | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.208-698_208-695dup others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr16 | 4651264 | |||||
chr16:4651284
|
A | G | 3 | a0001c0001t0002g0105a0001c0001t0006g0154a0001c0001t0008g0035 | 3 | HG02965.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.208-679A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651284 | ||||||
chr16:4651346
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.208-617C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651346 | ||||||
chr16:4651348
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.208-615G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651348 | ||||||
chr16:4651349
|
G | A | 1 | a0001c0001t0006g0132 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.208-614G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651349 | ||||||
chr16:4651361
|
A | G | 3 | a0001c0001t0006g0133a0001c0001t0006g0157a0001c0001t0006g0164 | 3 | HG00280.hp1 HG00323.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.208-602A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651361 | ||||||
chr16:4651408
|
G | A | 6 | a0001c0001t0032g0002a0001c0002t0003g0004a0001c0002t0003g0005others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-555G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651408 | ||||||
chr16:4651479
|
T | A | 48 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0001g0144others(45): Show | 48 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.208-484T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651479 | ||||||
chr16:4651565
|
G | C | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.208-398G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651565 | ||||||
chr16:4651574
|
G | A | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.208-389G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651574 | ||||||
chr16:4651578
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.208-385C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651578 | ||||||
chr16:4651584
|
G | T | 1 | a0001c0001t0019g0010 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.208-379G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651584 | ||||||
chr16:4651743
|
T | C | 48 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0001g0144others(45): Show | 48 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.208-220T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651743 | ||||||
chr16:4651773
|
C | T | 12 | a0001c0001t0001g0318a0001c0001t0002g0153a0001c0001t0002g0250others(9): Show | 12 | HG02071.hp1 HG02129.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.208-190C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651773 | ||||||
chr16:4651826
|
T | C | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.208-137T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651826 | ||||||
chr16:4651849
|
T | C | 14 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0001g0255others(11): Show | 14 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.208-114T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651849 | ||||||
chr16:4651855
|
T | G | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.208-108T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651855 | ||||||
chr16:4651858
|
A | G | 4 | a0001c0001t0002g0105a0001c0001t0006g0154a0001c0001t0008g0035others(1): Show | 4 | HG02965.hp2 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-105A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651858 | ||||||
chr16:4651859
|
T | G | 14 | a0001c0001t0001g0118a0001c0001t0001g0144a0001c0001t0001g0191others(11): Show | 14 | HG01099.hp1 HG01175.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.208-104T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651859 | ||||||
chr16:4651928
|
G | C | 1 | a0001c0001t0016g0054 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.208-35G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651928 | ||||||
chr16:4651930
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.208-33G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651930 | ||||||
chr16:4652066
|
C | A | 1 | a0001c0004t0036g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.296+15C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 3/16 | chr16 | 4652066 | ||||||
chr16:4652095
|
G | T | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.296+44G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 3/16 | chr16 | 4652095 | ||||||
chr16:4652101
|
T | A | 1 | a0001c0001t0005g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.296+50T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 3/16 | chr16 | 4652101 | ||||||
chr16:4652172
|
C | T | 2 | a0001c0001t0004g0017a0001c0003t0038g0018 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.296+121C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 3/16 | chr16 | 4652172 | ||||||
chr16:4652214
|
G | C | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.296+163G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 3/16 | chr16 | 4652214 | ||||||
chr16:4652474
|
G | A | 1 | a0001c0001t0003g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.297-204G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 3/16 | chr16 | 4652474 | ||||||
chr16:4652544
|
G | C | 1 | a0001c0001t0005g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.297-134G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 3/16 | chr16 | 4652544 | ||||||
chr16:4652546
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.297-132C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 3/16 | chr16 | 4652546 | ||||||
chr16:4652836
|
G | A | 1 | a0001c0001t0003g0056 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.443+12G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4652836 | ||||||
chr16:4652933
|
G | C | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.443+109G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4652933 | ||||||
chr16:4652942
|
C | T | 4 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0003t0018g0109others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+118C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4652942 | ||||||
chr16:4653012
|
C | CT | 4 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0003t0018g0109others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+189dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4653012 | |||||
chr16:4653081
|
C | A | 13 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(10): Show | 13 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.443+257C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653081 | ||||||
chr16:4653152
|
C | G | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02015.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.443+328C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653152 | ||||||
chr16:4653172
|
C | G | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.443+348C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653172 | ||||||
chr16:4653177
|
T | C | 12 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0004g0017others(9): Show | 12 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.443+353T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653177 | ||||||
chr16:4653491
|
TGTTTTGT others(4): Show |
T | 2 | a0001c0001t0029g0334a0001c0001t0035g0333 | 2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.443+668_443+678del others(11): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653491 | ||||||
chr16:4653539
|
C | T | 5 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0009g0075others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.443+715C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653539 | ||||||
chr16:4653596
|
C | CT | 4 | a0001c0001t0002g0105a0001c0001t0006g0154a0001c0001t0008g0035others(1): Show | 4 | HG02965.hp2 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+773dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4653596 | |||||
chr16:4653636
|
G | A | 8 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.443+812G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653636 | ||||||
chr16:4653715
|
C | T | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.443+891C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653715 | ||||||
chr16:4653832
|
A | C | 1 | a0001c0001t0003g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.443+1008A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653832 | ||||||
chr16:4653848
|
G | T | 1 | a0001c0001t0001g0239 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.443+1024G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653848 | ||||||
chr16:4653878
|
G | A | 2 | a0001c0001t0001g0249a0002c0009t0001g0248 | 2 | NA18977.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.443+1054G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653878 | ||||||
chr16:4653942
|
G | A | 14 | a0001c0001t0001g0118a0001c0001t0001g0144a0001c0001t0001g0191others(11): Show | 14 | HG01175.hp1 HG01243.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.443+1118G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653942 | ||||||
chr16:4653957
|
G | A | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.443+1133G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653957 | ||||||
chr16:4653969
|
C | G | 2 | a0001c0001t0032g0002a0001c0004t0036g0087 | 2 | HG01884.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.443+1145C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653969 | ||||||
chr16:4653976
|
G | A | 3 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0034 | 3 | HG02647.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.443+1152G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653976 | ||||||
chr16:4654083
|
C | T | 1 | a0001c0001t0007g0159 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.443+1259C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654083 | ||||||
chr16:4654085
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.443+1261G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654085 | ||||||
chr16:4654129
|
C | G | 4 | a0001c0001t0004g0011a0001c0001t0014g0019a0001c0001t0014g0020others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.443+1305C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654129 | ||||||
chr16:4654172
|
C | T | 7 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(4): Show | 7 | HG01099.hp1 HG01884.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.443+1348C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654172 | ||||||
chr16:4654192
|
A | G | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.443+1368A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654192 | ||||||
chr16:4654223
|
C | G | 7 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(4): Show | 7 | HG01099.hp1 HG01884.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.443+1399C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654223 | ||||||
chr16:4654432
|
T | G | 13 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(10): Show | 13 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.443+1608T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654432 | ||||||
chr16:4654466
|
T | C | 36 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0001g0144others(33): Show | 36 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.443+1642T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654466 | ||||||
chr16:4654666
|
C | T | 2 | a0001c0001t0004g0017a0001c0003t0038g0018 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.443+1842C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654666 | ||||||
chr16:4654729
|
G | A | 4 | a0001c0001t0002g0105a0001c0001t0006g0154a0001c0001t0008g0035others(1): Show | 4 | HG02965.hp2 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+1905G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654729 | ||||||
chr16:4654744
|
T | A | 43 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0001g0144others(40): Show | 43 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.443+1920T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654744 | ||||||
chr16:4654768
|
T | C | 27 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0001g0144others(24): Show | 27 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.443+1944T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654768 | ||||||
chr16:4654782
|
G | T | 9 | a0001c0001t0001g0118a0001c0001t0001g0144a0001c0001t0001g0191others(6): Show | 9 | HG01099.hp1 HG01175.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.443+1958G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654782 | ||||||
chr16:4654800
|
A | G | 1 | a0003c0007t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.443+1976A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654800 | ||||||
chr16:4654908
|
T | C | 17 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0001g0144others(14): Show | 17 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.443+2084T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654908 | ||||||
chr16:4654925
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.443+2101G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654925 | ||||||
chr16:4655015
|
A | T | 4 | a0001c0001t0004g0011a0001c0001t0014g0019a0001c0001t0014g0020others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.443+2191A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655015 | ||||||
chr16:4655022
|
G | C | 1 | a0001c0001t0019g0010 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.443+2198G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655022 | ||||||
chr16:4655028
|
G | A | 1 | a0003c0007t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.443+2204G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655028 | ||||||
chr16:4655099
|
T | A | 4 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0003t0018g0109others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-2147T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655099 | ||||||
chr16:4655138
|
G | A | 1 | a0001c0002t0005g0001 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.444-2108G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655138 | ||||||
chr16:4655183
|
C | A | 4 | a0001c0001t0008g0023a0001c0001t0008g0024a0001c0001t0008g0025others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.444-2063C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655183 | ||||||
chr16:4655236
|
G | A | 1 | a0001c0001t0003g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.444-2010G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655236 | ||||||
chr16:4655279
|
A | G | 7 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(4): Show | 7 | HG01099.hp1 HG01884.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.444-1967A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655279 | ||||||
chr16:4655297
|
G | A | 13 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(10): Show | 13 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.444-1949G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655297 | ||||||
chr16:4655381
|
C | G | 7 | a0001c0001t0004g0017a0001c0001t0032g0002a0001c0002t0003g0004others(4): Show | 7 | HG01099.hp1 HG01884.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.444-1865C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655381 | ||||||
chr16:4655381
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.444-1865C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655381 | ||||||
chr16:4655408
|
G | T | 4 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0003t0018g0109others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-1838G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655408 | ||||||
chr16:4655416
|
C | A | 1 | a0001c0001t0002g0260 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.444-1830C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655416 | ||||||
chr16:4655447
|
CT | C | 5 | a0001c0001t0001g0111a0001c0001t0001g0223a0001c0001t0019g0010others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.444-1798delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655447 | ||||||
chr16:4655458
|
AATCACAG others(75): Show |
A | 1 | a0001c0001t0006g0252 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.444-1746_444-1665d others(84): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4655458 | |||||
chr16:4655574
|
C | T | 2 | a0001c0001t0004g0068a0001c0001t0004g0069 | 2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.444-1672C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655574 | ||||||
chr16:4655597
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.444-1649G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655597 | ||||||
chr16:4655622
|
C | T | 13 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(10): Show | 13 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.444-1624C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655622 | ||||||
chr16:4655702
|
G | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0212 | 2 | HG00735.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.444-1544G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655702 | ||||||
chr16:4655945
|
G | A | 13 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(10): Show | 13 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.444-1301G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655945 | ||||||
chr16:4655946
|
G | T | 1 | a0001c0006t0009g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.444-1300G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655946 | ||||||
chr16:4655986
|
G | A | 3 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0281 | 3 | HG01975.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.444-1260G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655986 | ||||||
chr16:4656097
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.444-1149C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656097 | ||||||
chr16:4656179
|
A | C | 5 | a0001c0001t0001g0193a0001c0001t0001g0201a0001c0001t0001g0231others(2): Show | 5 | HG01106.hp1 HG01243.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.444-1067A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656179 | ||||||
chr16:4656302
|
A | G | 198 | a0001c0001t0001g0108a0001c0001t0001g0118a0001c0001t0001g0122others(195): Show | 198 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.444-944A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656302 | ||||||
chr16:4656316
|
A | T | 4 | a0001c0001t0001g0118a0001c0001t0001g0144a0001c0001t0016g0070others(1): Show | 4 | HG01175.hp1 HG02622.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.444-930A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656316 | ||||||
chr16:4656330
|
A | C | 37 | a0001c0001t0001g0118a0001c0001t0001g0144a0001c0001t0001g0191others(34): Show | 37 | HG01099.hp1 HG01175.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.444-916A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656330 | ||||||
chr16:4656356
|
G | A | 4 | a0001c0001t0001g0193a0001c0001t0001g0201a0001c0001t0001g0231others(1): Show | 4 | HG01106.hp1 HG01243.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-890G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656356 | ||||||
chr16:4656565
|
C | G | 2 | a0001c0001t0003g0009a0001c0001t0025g0031 | 2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.444-681C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656565 | ||||||
chr16:4656710
|
A | G | 11 | a0001c0001t0001g0118a0001c0001t0001g0144a0001c0001t0001g0191others(8): Show | 11 | HG01175.hp1 HG01243.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.444-536A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656710 | ||||||
chr16:4656787
|
G | T | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.444-459G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656787 | ||||||
chr16:4656882
|
A | AAAAT | 4 | a0001c0001t0002g0153a0001c0001t0002g0233a0001c0001t0002g0250others(1): Show | 4 | HG01175.hp2 HG02976.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.444-320_444-317dup others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4656882 | |||||
chr16:4656882
|
AAAAT | A | 53 | a0001c0001t0001g0129a0001c0001t0001g0146a0001c0001t0001g0188others(50): Show | 53 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.444-320_444-317del others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4656882 | |||||
chr16:4656882
|
AAAATAAA others(1): Show |
A | 132 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0108others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.444-324_444-317del others(8): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4656882 | |||||
chr16:4656882
|
AAAATAAA others(5): Show |
A | 93 | a0001c0001t0001g0106a0001c0001t0001g0134a0001c0001t0001g0286others(90): Show | 93 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.444-328_444-317del others(12): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4656882 | |||||
chr16:4656882
|
AAAATAAA others(9): Show |
A | 25 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(22): Show | 25 | HG00558.hp1 HG01099.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.444-332_444-317del others(16): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4656882 | |||||
chr16:4656882
|
AAAATAAA others(13): Show |
A | 1 | a0001c0001t0001g0213 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.444-336_444-317del others(20): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4656882 | |||||
chr16:4656910
|
T | C | 1 | a0001c0001t0006g0309 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.444-336T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656910 | ||||||
chr16:4656926
|
T | C | 3 | a0001c0001t0003g0065a0001c0001t0008g0022a0001c0001t0032g0002 | 3 | HG01884.hp1 HG02896.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.444-320T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656926 | ||||||
chr16:4656938
|
C | T | 1 | a0001c0001t0002g0282 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.444-308C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656938 | ||||||
chr16:4656945
|
C | T | 1 | a0001c0001t0059g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.444-301C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656945 | ||||||
chr16:4657019
|
T | C | 29 | a0001c0001t0001g0118a0001c0001t0001g0144a0001c0001t0001g0191others(26): Show | 29 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.444-227T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4657019 | ||||||
chr16:4657083
|
G | A | 1 | a0001c0001t0002g0308 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.444-163G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4657083 | ||||||
chr16:4657186
|
A | C | 9 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(6): Show | 9 | HG01099.hp1 HG01884.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.444-60A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4657186 | ||||||
chr16:4657225
|
C | G | 1 | a0001c0001t0001g0229 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.444-21C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4657225 | ||||||
chr16:4657379
|
C | T | 4 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0008g0024others(1): Show | 4 | HG00408.hp2 HG00621.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+16C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657379 | ||||||
chr16:4657431
|
A | G | 110 | a0001c0001t0001g0107a0001c0001t0001g0122a0001c0001t0001g0128others(107): Show | 110 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.561+68A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657431 | ||||||
chr16:4657516
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02015.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.561+153G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657516 | ||||||
chr16:4657593
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0181 | 2 | HG00735.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.561+230G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657593 | ||||||
chr16:4657738
|
C | CT | 101 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0108others(98): Show | 101 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.561+402dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4657738 | |||||
chr16:4657738
|
C | CTT | 26 | a0001c0001t0001g0161a0001c0001t0001g0181a0001c0001t0001g0277others(23): Show | 26 | HG00544.hp2 HG00735.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.561+401_561+402dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4657738 | |||||
chr16:4657738
|
C | CTTTTTTT others(8): Show |
1 | a0001c0003t0018g0110 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.561+388_561+402dup others(15): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4657738 | |||||
chr16:4657738
|
C | CTTTTTTT others(9): Show |
1 | a0001c0003t0018g0109 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.561+387_561+402dup others(16): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4657738 | |||||
chr16:4657738
|
CT | C | 37 | a0001c0001t0001g0188a0001c0001t0001g0212a0001c0001t0001g0213others(34): Show | 37 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.561+402delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4657738 | |||||
chr16:4657738
|
CTT | C | 7 | a0001c0001t0001g0217a0001c0001t0001g0220a0001c0001t0004g0011others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.561+401_561+402del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4657738 | |||||
chr16:4657738
|
CTTT | C | 10 | a0001c0001t0001g0118a0001c0001t0001g0144a0001c0001t0001g0191others(7): Show | 10 | HG01175.hp1 HG02622.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.561+400_561+402del others(3): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4657738 | |||||
chr16:4657763
|
T | G | 1 | a0001c0001t0001g0178 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.561+400T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657763 | ||||||
chr16:4657784
|
C | G | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.561+421C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657784 | ||||||
chr16:4657784
|
C | T | 1 | a0001c0001t0003g0056 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.561+421C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657784 | ||||||
chr16:4657807
|
G | A | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.561+444G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657807 | ||||||
chr16:4657808
|
C | T | 3 | a0001c0001t0003g0009a0001c0001t0025g0031a0001c0001t0032g0002 | 3 | HG01884.hp1 HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.561+445C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657808 | ||||||
chr16:4657814
|
C | T | 1 | a0001c0001t0007g0167 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.561+451C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657814 | ||||||
chr16:4657848
|
G | C | 40 | a0001c0001t0001g0118a0001c0001t0001g0144a0001c0001t0001g0191others(37): Show | 40 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.561+485G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657848 | ||||||
chr16:4657932
|
C | T | 25 | a0001c0001t0001g0118a0001c0001t0001g0144a0001c0001t0001g0191others(22): Show | 25 | HG01099.hp1 HG01175.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.561+569C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657932 | ||||||
chr16:4657943
|
C | T | 2 | a0001c0001t0007g0148a0001c0001t0007g0167 | 2 | HG01074.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.561+580C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657943 | ||||||
chr16:4657979
|
T | A | 26 | a0001c0001t0001g0118a0001c0001t0001g0144a0001c0001t0001g0191others(23): Show | 26 | HG01099.hp1 HG01175.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.561+616T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657979 | ||||||
chr16:4657985
|
G | A | 26 | a0001c0001t0001g0118a0001c0001t0001g0144a0001c0001t0001g0191others(23): Show | 26 | HG01099.hp1 HG01175.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.561+622G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657985 | ||||||
chr16:4658033
|
T | C | 7 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(4): Show | 7 | HG01099.hp1 HG01884.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.561+670T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658033 | ||||||
chr16:4658110
|
T | C | 26 | a0001c0001t0001g0118a0001c0001t0001g0144a0001c0001t0001g0191others(23): Show | 26 | HG01099.hp1 HG01175.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.561+747T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658110 | ||||||
chr16:4658179
|
C | G | 4 | a0001c0001t0001g0118a0001c0001t0001g0144a0001c0001t0001g0191others(1): Show | 4 | HG01175.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+816C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658179 | ||||||
chr16:4658241
|
A | G | 1 | a0001c0001t0002g0171 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.561+878A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658241 | ||||||
chr16:4658263
|
C | T | 2 | a0001c0001t0003g0078a0001c0001t0003g0079 | 2 | NA18977.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.561+900C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658263 | ||||||
chr16:4658273
|
T | C | 1 | a0001c0001t0049g0196 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.561+910T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658273 | ||||||
chr16:4658278
|
G | A | 1 | a0001c0001t0040g0315 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.561+915G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658278 | ||||||
chr16:4658376
|
A | G | 1 | a0001c0001t0002g0226 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.561+1013A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658376 | ||||||
chr16:4658404
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.561+1041C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658404 | ||||||
chr16:4658428
|
G | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.561+1065G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658428 | ||||||
chr16:4658484
|
C | T | 2 | a0001c0001t0004g0068a0001c0001t0004g0069 | 2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.561+1121C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658484 | ||||||
chr16:4658487
|
G | A | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.561+1124G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658487 | ||||||
chr16:4658493
|
G | A | 1 | a0001c0001t0004g0080 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.561+1130G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658493 | ||||||
chr16:4658522
|
T | C | 141 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.561+1159T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658522 | ||||||
chr16:4658537
|
G | GA | 29 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(26): Show | 29 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.561+1186dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4658537 | |||||
chr16:4658538
|
A | G | 1 | a0001c0001t0002g0325 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.561+1175A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658538 | ||||||
chr16:4658541
|
A | AG | 129 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.561+1178_561+1179i others(3): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658541 | ||||||
chr16:4658736
|
G | A | 1 | a0001c0001t0006g0132 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.561+1373G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658736 | ||||||
chr16:4658958
|
G | C | 157 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.561+1595G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658958 | ||||||
chr16:4658969
|
C | T | 1 | a0001c0001t0044g0139 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.561+1606C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658969 | ||||||
chr16:4659093
|
T | C | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.561+1730T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659093 | ||||||
chr16:4659130
|
C | A | 145 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.561+1767C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659130 | ||||||
chr16:4659160
|
TA | T | 157 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.561+1807delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4659160 | |||||
chr16:4659249
|
G | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0328 | 2 | NA18966.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.561+1886G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659249 | ||||||
chr16:4659284
|
C | A | 1 | a0001c0001t0023g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.561+1921C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659284 | ||||||
chr16:4659417
|
G | A | 1 | a0001c0001t0023g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.561+2054G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659417 | ||||||
chr16:4659458
|
T | G | 192 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0108others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.561+2095T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659458 | ||||||
chr16:4659503
|
T | C | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.561+2140T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659503 | ||||||
chr16:4659578
|
C | A | 1 | a0001c0001t0023g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.561+2215C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659578 | ||||||
chr16:4659625
|
C | T | 3 | a0001c0001t0001g0261a0001c0001t0001g0266a0001c0001t0001g0267 | 3 | HG00673.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.561+2262C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659625 | ||||||
chr16:4659635
|
A | G | 167 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.561+2272A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659635 | ||||||
chr16:4659675
|
G | A | 1 | a0001c0001t0002g0202 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.561+2312G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659675 | ||||||
chr16:4659963
|
T | C | 31 | a0001c0001t0001g0118a0001c0001t0001g0144a0001c0001t0001g0191others(28): Show | 31 | HG01099.hp1 HG01175.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.561+2600T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659963 | ||||||
chr16:4659992
|
C | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.561+2629C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659992 | ||||||
chr16:4660008
|
C | T | 1 | a0001c0001t0003g0097 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.561+2645C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660008 | ||||||
chr16:4660097
|
C | T | 1 | a0001c0001t0003g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.561+2734C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660097 | ||||||
chr16:4660192
|
C | T | 1 | a0001c0001t0003g0097 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.561+2829C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660192 | ||||||
chr16:4660218
|
A | G | 1 | a0001c0001t0016g0054 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.561+2855A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660218 | ||||||
chr16:4660240
|
G | A | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.561+2877G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660240 | ||||||
chr16:4660276
|
G | A | 2 | a0001c0001t0009g0075a0001c0001t0009g0076 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.561+2913G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660276 | ||||||
chr16:4660294
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.561+2931G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660294 | ||||||
chr16:4660338
|
T | A | 16 | a0001c0001t0003g0013a0001c0001t0004g0011a0001c0001t0005g0036others(13): Show | 16 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.561+2975T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660338 | ||||||
chr16:4660348
|
C | T | 1 | a0001c0001t0016g0054 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.561+2985C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660348 | ||||||
chr16:4660349
|
G | A | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.561+2986G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660349 | ||||||
chr16:4660364
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.561+3001G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660364 | ||||||
chr16:4660376
|
G | C | 2 | a0001c0001t0002g0142a0001c0001t0062g0143 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.561+3013G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660376 | ||||||
chr16:4660381
|
T | A | 1 | a0001c0004t0036g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.561+3018T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660381 | ||||||
chr16:4660403
|
C | T | 1 | a0001c0001t0031g0046 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.561+3040C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660403 | ||||||
chr16:4660492
|
A | G | 7 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(4): Show | 7 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.561+3129A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660492 | ||||||
chr16:4660589
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.561+3226C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660589 | ||||||
chr16:4660607
|
C | T | 3 | a0001c0001t0006g0154a0001c0001t0008g0035a0001c0001t0027g0045 | 3 | HG03139.hp2 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.561+3244C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660607 | ||||||
chr16:4660609
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.561+3246C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660609 | ||||||
chr16:4660621
|
C | T | 1 | a0001c0001t0021g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.561+3258C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660621 | ||||||
chr16:4660622
|
G | T | 1 | a0001c0001t0015g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.561+3259G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660622 | ||||||
chr16:4660636
|
T | G | 1 | a0001c0001t0002g0184 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.561+3273T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660636 | ||||||
chr16:4660646
|
G | A | 1 | a0001c0001t0008g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.561+3283G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660646 | ||||||
chr16:4660772
|
T | C | 13 | a0001c0001t0004g0011a0001c0001t0005g0036a0001c0001t0005g0037others(10): Show | 13 | HG01243.hp1 HG01891.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.561+3409T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660772 | ||||||
chr16:4660778
|
CAG | C | 133 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.561+3416_561+3417d others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660778 | ||||||
chr16:4660897
|
T | G | 234 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.561+3534T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660897 | ||||||
chr16:4660982
|
A | G | 1 | a0001c0001t0011g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.561+3619A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660982 | ||||||
chr16:4661024
|
C | G | 3 | a0001c0001t0014g0019a0001c0001t0014g0020a0001c0001t0033g0021 | 3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.561+3661C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661024 | ||||||
chr16:4661034
|
T | C | 1 | a0001c0003t0038g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.561+3671T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661034 | ||||||
chr16:4661143
|
AT | A | 142 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.562-3551delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4661143 | |||||
chr16:4661249
|
G | A | 3 | a0001c0001t0006g0154a0001c0001t0008g0035a0001c0001t0027g0045 | 3 | HG03139.hp2 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.562-3460G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661249 | ||||||
chr16:4661270
|
C | T | 3 | a0001c0001t0001g0264a0001c0001t0023g0006a0001c0001t0029g0334 | 3 | HG02922.hp1 HG03471.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.562-3439C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661270 | ||||||
chr16:4661325
|
G | C | 174 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.562-3384G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661325 | ||||||
chr16:4661344
|
C | T | 2 | a0001c0001t0008g0035a0001c0001t0027g0045 | 2 | HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.562-3365C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661344 | ||||||
chr16:4661357
|
C | CGCACCCT others(8): Show |
1 | a0001c0001t0002g0112 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.562-3344_562-3330d others(17): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4661357 | |||||
chr16:4661392
|
C | T | 115 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0108others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.562-3317C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661392 | ||||||
chr16:4661405
|
G | T | 2 | a0001c0001t0013g0194a0001c0001t0016g0054 | 2 | HG01515.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.562-3304G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661405 | ||||||
chr16:4661407
|
C | T | 3 | a0001c0001t0006g0154a0001c0001t0008g0035a0001c0001t0027g0045 | 3 | HG03139.hp2 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.562-3302C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661407 | ||||||
chr16:4661511
|
C | T | 11 | a0001c0001t0004g0011a0001c0001t0005g0036a0001c0001t0005g0037others(8): Show | 11 | HG01243.hp1 HG01891.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.562-3198C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661511 | ||||||
chr16:4661630
|
C | T | 1 | a0001c0001t0019g0010 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.562-3079C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661630 | ||||||
chr16:4661642
|
C | G | 1 | a0001c0004t0036g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.562-3067C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661642 | ||||||
chr16:4661736
|
T | G | 157 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.562-2973T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661736 | ||||||
chr16:4661790
|
C | T | 140 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.562-2919C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661790 | ||||||
chr16:4661814
|
G | A | 1 | a0001c0001t0025g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.562-2895G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661814 | ||||||
chr16:4661863
|
T | G | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.562-2846T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661863 | ||||||
chr16:4661902
|
T | A | 4 | a0001c0003t0018g0109a0001c0003t0018g0110a0001c0003t0038g0018others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.562-2807T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661902 | ||||||
chr16:4662055
|
G | A | 5 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.562-2654G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662055 | ||||||
chr16:4662147
|
G | A | 140 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.562-2562G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662147 | ||||||
chr16:4662177
|
T | G | 1 | a0001c0003t0038g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.562-2532T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662177 | ||||||
chr16:4662306
|
G | A | 1 | a0001c0001t0003g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.562-2403G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662306 | ||||||
chr16:4662311
|
T | C | 1 | a0001c0001t0002g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.562-2398T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662311 | ||||||
chr16:4662400
|
C | T | 127 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.562-2309C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662400 | ||||||
chr16:4662459
|
C | T | 8 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.562-2250C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662459 | ||||||
chr16:4662515
|
CA | C | 8 | a0001c0001t0001g0156a0001c0001t0001g0223a0001c0001t0003g0007others(5): Show | 8 | HG02155.hp1 HG02486.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.562-2179delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4662515 | |||||
chr16:4662543
|
TACTC | T | 3 | a0001c0001t0004g0057a0001c0001t0004g0063a0001c0001t0014g0055 | 3 | NA18967.hp1 NA18971.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.562-2163_562-2160d others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4662543 | |||||
chr16:4662549
|
C | A | 1 | a0001c0001t0026g0081 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.562-2160C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662549 | ||||||
chr16:4662790
|
G | C | 1 | a0001c0001t0019g0010 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.562-1919G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662790 | ||||||
chr16:4662845
|
G | C | 1 | a0001c0001t0001g0163 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.562-1864G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662845 | ||||||
chr16:4662939
|
C | G | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.562-1770C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662939 | ||||||
chr16:4662950
|
G | T | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.562-1759G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662950 | ||||||
chr16:4663086
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.562-1623C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663086 | ||||||
chr16:4663114
|
A | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.562-1595A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663114 | ||||||
chr16:4663123
|
G | C | 11 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(8): Show | 11 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.562-1586G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663123 | ||||||
chr16:4663132
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.562-1577C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663132 | ||||||
chr16:4663225
|
G | C | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.562-1484G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663225 | ||||||
chr16:4663295
|
C | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.562-1414C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663295 | ||||||
chr16:4663300
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.562-1409G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663300 | ||||||
chr16:4663358
|
T | C | 6 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.562-1351T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663358 | ||||||
chr16:4663365
|
G | GT | 106 | a0001c0001t0001g0134a0001c0001t0001g0146a0001c0001t0001g0188others(103): Show | 106 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.562-1318dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4663365 | |||||
chr16:4663365
|
G | GTT | 46 | a0001c0001t0001g0213a0001c0001t0001g0217a0001c0001t0001g0229others(43): Show | 46 | HG00544.hp1 HG00544.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.562-1319_562-1318d others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4663365 | |||||
chr16:4663365
|
G | GTTT | 22 | a0001c0001t0001g0220a0001c0001t0002g0104a0001c0001t0002g0166others(19): Show | 22 | HG00558.hp1 HG01123.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.562-1320_562-1318d others(5): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4663365 | |||||
chr16:4663365
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0001g0144 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.562-1327_562-1318d others(12): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4663365 | |||||
chr16:4663391
|
T | A | 1 | a0001c0001t0001g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.562-1318T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663391 | ||||||
chr16:4663391
|
T | TTTTA | 92 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0108others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.562-1318_562-1317i others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663391 | ||||||
chr16:4663391
|
T | TTTTTA | 20 | a0001c0001t0001g0115a0001c0001t0001g0136a0001c0001t0001g0172others(17): Show | 20 | HG00408.hp2 HG00423.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.562-1318_562-1317i others(7): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663391 | ||||||
chr16:4663435
|
G | A | 1 | a0001c0001t0056g0317 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.562-1274G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663435 | ||||||
chr16:4663527
|
A | G | 1 | a0001c0001t0025g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.562-1182A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663527 | ||||||
chr16:4663607
|
G | C | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.562-1102G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663607 | ||||||
chr16:4663634
|
A | T | 2 | a0001c0001t0003g0013a0001c0001t0022g0014 | 2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.562-1075A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663634 | ||||||
chr16:4663757
|
C | T | 1 | a0001c0001t0006g0309 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.562-952C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663757 | ||||||
chr16:4663915
|
C | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0224 | 2 | HG00099.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.562-794C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663915 | ||||||
chr16:4663923
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.562-786C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663923 | ||||||
chr16:4663929
|
G | T | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.562-780G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663929 | ||||||
chr16:4663934
|
C | A | 6 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.562-775C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663934 | ||||||
chr16:4664105
|
G | A | 3 | a0001c0001t0014g0019a0001c0001t0014g0020a0001c0001t0033g0021 | 3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.562-604G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664105 | ||||||
chr16:4664138
|
C | G | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.562-571C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664138 | ||||||
chr16:4664138
|
C | T | 12 | a0001c0001t0002g0130a0001c0001t0005g0036a0001c0001t0005g0037others(9): Show | 12 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.562-571C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664138 | ||||||
chr16:4664183
|
G | A | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.562-526G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664183 | ||||||
chr16:4664346
|
G | T | 3 | a0001c0001t0004g0011a0001c0001t0023g0006a0001c0001t0029g0334 | 3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.562-363G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664346 | ||||||
chr16:4664364
|
T | C | 163 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.562-345T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664364 | ||||||
chr16:4664391
|
C | T | 1 | a0001c0001t0025g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.562-318C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664391 | ||||||
chr16:4664552
|
C | T | 1 | a0001c0001t0001g0311 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.562-157C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664552 | ||||||
chr16:4664577
|
C | T | 11 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(8): Show | 11 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.562-132C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664577 | ||||||
chr16:4664638
|
T | C | 163 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.562-71T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664638 | ||||||
chr16:4664835
|
T | C | 4 | a0001c0003t0018g0109a0001c0003t0018g0110a0001c0003t0038g0018others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+60T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 6/16 | chr16 | 4664835 | ||||||
chr16:4664864
|
A | C | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.628+89A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 6/16 | chr16 | 4664864 | ||||||
chr16:4664997
|
G | A | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.629-105G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 6/16 | chr16 | 4664997 | ||||||
chr16:4665009
|
C | T | 1 | a0001c0006t0009g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.629-93C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 6/16 | chr16 | 4665009 | ||||||
chr16:4665011
|
C | T | 140 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.629-91C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 6/16 | chr16 | 4665011 | ||||||
chr16:4665013
|
G | C | 1 | a0001c0001t0029g0334 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.629-89G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 6/16 | chr16 | 4665013 | ||||||
chr16:4665218
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.678+67C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665218 | ||||||
chr16:4665318
|
C | G | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.678+167C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665318 | ||||||
chr16:4665339
|
G | A | 2 | a0001c0001t0001g0286a0001c0001t0039g0145 | 2 | HG01123.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.678+188G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665339 | ||||||
chr16:4665362
|
CT | C | 16 | a0001c0001t0002g0142a0001c0001t0005g0036a0001c0001t0005g0037others(13): Show | 16 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.678+226delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr16 | 4665362 | |||||
chr16:4665418
|
T | C | 4 | a0001c0003t0018g0109a0001c0003t0018g0110a0001c0003t0038g0018others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.678+267T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665418 | ||||||
chr16:4665426
|
G | A | 1 | a0001c0001t0029g0334 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.678+275G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665426 | ||||||
chr16:4665509
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.678+358C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665509 | ||||||
chr16:4665667
|
C | CT | 47 | a0001c0001t0001g0103a0001c0001t0001g0137a0001c0001t0001g0172others(44): Show | 47 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.678+536dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr16 | 4665667 | |||||
chr16:4665667
|
CT | C | 6 | a0001c0001t0001g0188a0001c0001t0002g0149a0001c0001t0004g0011others(3): Show | 6 | HG01069.hp1 HG01243.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.678+536delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr16 | 4665667 | |||||
chr16:4665668
|
T | C | 1 | a0001c0001t0002g0226 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.678+517T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665668 | ||||||
chr16:4665669
|
T | C | 1 | a0001c0001t0002g0276 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.678+518T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665669 | ||||||
chr16:4665704
|
C | G | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.678+553C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665704 | ||||||
chr16:4665833
|
C | G | 1 | a0001c0001t0023g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.678+682C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665833 | ||||||
chr16:4665912
|
C | T | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.678+761C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665912 | ||||||
chr16:4665969
|
A | G | 1 | a0001c0001t0002g0142 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.678+818A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665969 | ||||||
chr16:4665976
|
C | A | 1 | a0001c0001t0001g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.678+825C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665976 | ||||||
chr16:4666061
|
C | T | 132 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.678+910C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666061 | ||||||
chr16:4666075
|
T | C | 4 | a0001c0003t0018g0109a0001c0003t0018g0110a0001c0003t0038g0018others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.678+924T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666075 | ||||||
chr16:4666102
|
T | C | 147 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.678+951T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666102 | ||||||
chr16:4666123
|
C | T | 1 | a0001c0001t0002g0306 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.678+972C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666123 | ||||||
chr16:4666202
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.678+1051G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666202 | ||||||
chr16:4666209
|
C | A | 1 | a0001c0001t0011g0301 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.678+1058C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666209 | ||||||
chr16:4666225
|
T | C | 2 | a0001c0001t0014g0096a0001c0001t0058g0329 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.678+1074T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666225 | ||||||
chr16:4666253
|
C | T | 132 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.678+1102C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666253 | ||||||
chr16:4666291
|
T | G | 4 | a0001c0003t0018g0109a0001c0003t0018g0110a0001c0003t0038g0018others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.678+1140T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666291 | ||||||
chr16:4666316
|
G | C | 1 | a0001c0001t0002g0324 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.678+1165G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666316 | ||||||
chr16:4666328
|
C | T | 1 | a0001c0001t0019g0010 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.678+1177C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666328 | ||||||
chr16:4666361
|
G | T | 5 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.678+1210G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666361 | ||||||
chr16:4666516
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0168 | 2 | NA18978.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.678+1365G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666516 | ||||||
chr16:4666543
|
A | T | 1 | a0001c0001t0002g0273 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.678+1392A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666543 | ||||||
chr16:4666616
|
G | A | 1 | a0001c0001t0008g0022 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.678+1465G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666616 | ||||||
chr16:4666633
|
T | C | 4 | a0001c0003t0018g0109a0001c0003t0018g0110a0001c0003t0038g0018others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.678+1482T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666633 | ||||||
chr16:4666754
|
CA | C | 5 | a0001c0001t0002g0198a0001c0001t0002g0216a0001c0001t0002g0232others(2): Show | 5 | NA18942.hp2 NA18995.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.679-1510delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666754 | ||||||
chr16:4666760
|
C | G | 4 | a0001c0003t0018g0109a0001c0003t0018g0110a0001c0003t0038g0018others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-1505C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666760 | ||||||
chr16:4666889
|
A | G | 239 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.679-1376A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666889 | ||||||
chr16:4666926
|
C | G | 1 | a0001c0001t0006g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.679-1339C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666926 | ||||||
chr16:4666968
|
C | T | 3 | a0001c0001t0014g0019a0001c0001t0014g0020a0001c0001t0033g0021 | 3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.679-1297C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666968 | ||||||
chr16:4666973
|
G | C | 11 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(8): Show | 11 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.679-1292G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666973 | ||||||
chr16:4666991
|
T | C | 11 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(8): Show | 11 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.679-1274T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666991 | ||||||
chr16:4667028
|
G | A | 1 | a0001c0001t0059g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.679-1237G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667028 | ||||||
chr16:4667059
|
G | A | 1 | a0001c0001t0019g0010 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.679-1206G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667059 | ||||||
chr16:4667074
|
T | G | 3 | a0001c0001t0004g0011a0001c0001t0023g0006a0001c0001t0029g0334 | 3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.679-1191T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667074 | ||||||
chr16:4667085
|
C | T | 2 | a0001c0003t0038g0018a0001c0004t0036g0087 | 2 | HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.679-1180C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667085 | ||||||
chr16:4667140
|
C | T | 11 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(8): Show | 11 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.679-1125C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667140 | ||||||
chr16:4667144
|
G | T | 1 | a0001c0001t0001g0156 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.679-1121G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667144 | ||||||
chr16:4667339
|
G | C | 4 | a0001c0003t0018g0109a0001c0003t0018g0110a0001c0003t0038g0018others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-926G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667339 | ||||||
chr16:4667396
|
G | A | 1 | a0001c0001t0011g0290 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.679-869G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667396 | ||||||
chr16:4667446
|
C | T | 2 | a0001c0001t0002g0325a0001c0001t0003g0051 | 2 | HG00597.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.679-819C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667446 | ||||||
chr16:4667452
|
C | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.679-813C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667452 | ||||||
chr16:4667467
|
T | C | 3 | a0001c0001t0004g0011a0001c0001t0023g0006a0001c0001t0029g0334 | 3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.679-798T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667467 | ||||||
chr16:4667550
|
A | G | 1 | a0001c0001t0001g0268 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.679-715A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667550 | ||||||
chr16:4667616
|
G | C | 1 | a0001c0001t0002g0233 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.679-649G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667616 | ||||||
chr16:4667685
|
C | T | 1 | a0003c0007t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.679-580C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667685 | ||||||
chr16:4667686
|
T | A | 3 | a0001c0001t0004g0011a0001c0001t0023g0006a0001c0001t0029g0334 | 3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.679-579T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667686 | ||||||
chr16:4667710
|
T | C | 7 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(4): Show | 7 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.679-555T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667710 | ||||||
chr16:4667895
|
G | C | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.679-370G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667895 | ||||||
chr16:4667964
|
C | T | 1 | a0001c0001t0030g0058 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.679-301C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667964 | ||||||
chr16:4668096
|
G | A | 1 | a0001c0001t0006g0252 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.679-169G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4668096 | ||||||
chr16:4668124
|
C | CT | 8 | a0001c0001t0001g0168a0001c0001t0001g0267a0001c0001t0002g0208others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.679-127dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr16 | 4668124 | |||||
chr16:4668124
|
CTT | C | 11 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(8): Show | 11 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.679-128_679-127del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr16 | 4668124 | |||||
chr16:4668194
|
A | T | 2 | a0001c0003t0038g0018a0001c0004t0036g0087 | 2 | HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.679-71A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4668194 | ||||||
chr16:4668387
|
A | G | 137 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.726+75A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668387 | ||||||
chr16:4668428
|
C | T | 1 | a0001c0001t0004g0050 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.726+116C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668428 | ||||||
chr16:4668429
|
GCTCATAC others(3): Show |
G | 1 | a0001c0001t0045g0200 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.726+128_726+137del others(10): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668429 | |||||
chr16:4668436
|
C | T | 3 | a0001c0001t0004g0011a0001c0001t0023g0006a0001c0001t0029g0334 | 3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.726+124C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668436 | ||||||
chr16:4668442
|
C | G | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.726+130C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668442 | ||||||
chr16:4668470
|
GAC | G | 5 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.726+164_726+165del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668470 | |||||
chr16:4668484
|
C | T | 3 | a0001c0001t0004g0011a0001c0001t0023g0006a0001c0001t0029g0334 | 3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.726+172C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668484 | ||||||
chr16:4668491
|
ACACT | A | 18 | a0001c0001t0001g0122a0001c0001t0001g0128a0001c0001t0001g0222others(15): Show | 18 | HG00621.hp2 HG02027.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.726+183_726+186del others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668491 | |||||
chr16:4668508
|
T | C | 4 | a0001c0003t0018g0109a0001c0003t0018g0110a0001c0003t0038g0018others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+196T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668508 | ||||||
chr16:4668540
|
T | C | 1 | a0001c0001t0016g0054 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.726+228T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668540 | ||||||
chr16:4668558
|
CCTA | C | 5 | a0001c0001t0006g0157a0001c0001t0032g0002a0001c0001t0048g0177others(2): Show | 5 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.726+249_726+251del others(3): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668558 | |||||
chr16:4668578
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0213 | 2 | HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.726+266C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668578 | ||||||
chr16:4668610
|
ACT | A | 4 | a0001c0003t0018g0109a0001c0003t0018g0110a0001c0003t0038g0018others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+300_726+301del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668610 | |||||
chr16:4668655
|
T | C | 158 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.726+343T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668655 | ||||||
chr16:4668669
|
CAT | C | 5 | a0001c0001t0001g0113a0001c0003t0018g0109a0001c0003t0018g0110others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.726+361_726+362del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668669 | |||||
chr16:4668677
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.726+365T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668677 | ||||||
chr16:4668702
|
A | G | 1 | a0001c0001t0023g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.726+390A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668702 | ||||||
chr16:4668710
|
ACACT | A | 10 | a0001c0001t0001g0108a0001c0001t0002g0112a0001c0001t0004g0011others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.726+406_726+409del others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668710 | |||||
chr16:4668727
|
C | T | 3 | a0001c0001t0001g0193a0001c0001t0012g0195a0001c0001t0013g0194 | 3 | HG01257.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.726+415C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668727 | ||||||
chr16:4668727
|
CAT | C | 4 | a0001c0003t0018g0109a0001c0003t0018g0110a0001c0003t0038g0018others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+417_726+418del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668727 | |||||
chr16:4668741
|
G | C | 5 | a0001c0001t0027g0045a0001c0003t0018g0109a0001c0003t0018g0110others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.726+429G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668741 | ||||||
chr16:4668762
|
T | TCA | 153 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.726+459_726+460dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668762 | |||||
chr16:4668769
|
C | CACACAG | 4 | a0001c0003t0018g0109a0001c0003t0018g0110a0001c0003t0038g0018others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+460_726+461ins others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668769 | |||||
chr16:4668796
|
A | G | 5 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0006g0158others(2): Show | 5 | HG00558.hp2 HG02155.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.726+484A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668796 | ||||||
chr16:4668904
|
G | A | 1 | a0001c0001t0034g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.726+592G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668904 | ||||||
chr16:4668935
|
C | T | 1 | a0001c0001t0006g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.726+623C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668935 | ||||||
chr16:4669009
|
GACAC | G | 134 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.726+705_726+708del others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4669009 | |||||
chr16:4669024
|
A | G | 1 | a0001c0001t0006g0252 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.726+712A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669024 | ||||||
chr16:4669036
|
A | G | 4 | a0001c0001t0001g0137a0001c0001t0001g0172a0001c0001t0001g0173others(1): Show | 4 | NA18939.hp2 NA18949.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+724A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669036 | ||||||
chr16:4669200
|
G | A | 1 | a0001c0001t0006g0132 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.726+888G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669200 | ||||||
chr16:4669348
|
G | C | 155 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.726+1036G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669348 | ||||||
chr16:4669370
|
G | T | 1 | a0001c0001t0006g0164 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.726+1058G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669370 | ||||||
chr16:4669383
|
G | A | 3 | a0001c0001t0004g0011a0001c0001t0023g0006a0001c0001t0029g0334 | 3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.726+1071G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669383 | ||||||
chr16:4669431
|
C | CA | 7 | a0001c0001t0002g0237a0001c0001t0002g0260a0001c0001t0003g0048others(4): Show | 7 | HG01123.hp1 HG02622.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.726+1136dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4669431 | |||||
chr16:4669431
|
C | CAAAAAAA others(4): Show |
9 | a0001c0001t0005g0036a0001c0001t0005g0038a0001c0001t0005g0039others(6): Show | 9 | HG02451.hp2 HG02486.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.726+1126_726+1136d others(13): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4669431 | |||||
chr16:4669431
|
C | CAAAAAAA others(5): Show |
96 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.726+1125_726+1136d others(14): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4669431 | |||||
chr16:4669431
|
C | CAAAAAAA others(6): Show |
37 | a0001c0001t0001g0113a0001c0001t0001g0122a0001c0001t0001g0128others(34): Show | 37 | HG00323.hp1 HG00323.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.726+1124_726+1136d others(15): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4669431 | |||||
chr16:4669431
|
C | CAAAAAAA others(7): Show |
10 | a0001c0001t0001g0136a0001c0001t0001g0168a0001c0001t0001g0207others(7): Show | 10 | HG00280.hp1 HG03688.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.726+1123_726+1136d others(16): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4669431 | |||||
chr16:4669431
|
C | CAAAAAAA others(12): Show |
2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.726+1136_726+1137i others(21): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4669431 | |||||
chr16:4669458
|
C | G | 159 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.726+1146C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669458 | ||||||
chr16:4669521
|
C | T | 3 | a0001c0001t0004g0011a0001c0001t0023g0006a0001c0001t0029g0334 | 3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.726+1209C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669521 | ||||||
chr16:4669526
|
A | G | 3 | a0001c0001t0004g0011a0001c0001t0023g0006a0001c0001t0029g0334 | 3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.726+1214A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669526 | ||||||
chr16:4669674
|
C | T | 1 | a0001c0001t0003g0008 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.726+1362C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669674 | ||||||
chr16:4669682
|
T | C | 2 | a0001c0001t0001g0249a0002c0009t0001g0248 | 2 | NA18977.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.726+1370T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669682 | ||||||
chr16:4669697
|
A | G | 1 | a0001c0001t0003g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.726+1385A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669697 | ||||||
chr16:4669748
|
T | C | 1 | a0001c0001t0003g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.726+1436T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669748 | ||||||
chr16:4669804
|
C | G | 1 | a0001c0001t0029g0334 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.726+1492C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669804 | ||||||
chr16:4669947
|
A | G | 4 | a0001c0001t0004g0011a0001c0001t0023g0006a0001c0001t0027g0045others(1): Show | 4 | HG01243.hp1 HG02922.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.727-1444A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669947 | ||||||
chr16:4669972
|
G | GT | 111 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.727-1417dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4669972 | |||||
chr16:4669980
|
G | A | 124 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.727-1411G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669980 | ||||||
chr16:4670093
|
C | T | 1 | a0001c0001t0029g0334 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.727-1298C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670093 | ||||||
chr16:4670127
|
C | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.727-1264C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670127 | ||||||
chr16:4670177
|
T | TGCC | 20 | a0001c0001t0003g0013a0001c0001t0004g0011a0001c0001t0005g0036others(17): Show | 20 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.727-1214_727-1213i others(5): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670177 | ||||||
chr16:4670373
|
G | C | 3 | a0001c0001t0004g0011a0001c0001t0027g0045a0001c0001t0029g0334 | 3 | HG01243.hp1 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.727-1018G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670373 | ||||||
chr16:4670389
|
C | T | 127 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.727-1002C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670389 | ||||||
chr16:4670432
|
G | C | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.727-959G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670432 | ||||||
chr16:4670546
|
A | G | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.727-845A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670546 | ||||||
chr16:4670673
|
A | G | 1 | a0001c0001t0006g0252 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.727-718A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670673 | ||||||
chr16:4670675
|
C | G | 1 | a0001c0001t0011g0291 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.727-716C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670675 | ||||||
chr16:4670743
|
CCAGGTCC others(3): Show |
C | 3 | a0001c0003t0018g0109a0001c0003t0018g0110a0001c0003t0038g0018 | 3 | HG01167.hp1 HG01169.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.727-642_727-633del others(10): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4670743 | |||||
chr16:4670789
|
C | T | 1 | a0001c0001t0005g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.727-602C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670789 | ||||||
chr16:4670795
|
C | T | 2 | a0001c0001t0002g0243a0001c0001t0003g0097 | 2 | HG01167.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.727-596C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670795 | ||||||
chr16:4670801
|
T | C | 5 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.727-590T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670801 | ||||||
chr16:4670818
|
C | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.727-573C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670818 | ||||||
chr16:4670921
|
C | T | 1 | a0001c0003t0038g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.727-470C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670921 | ||||||
chr16:4670982
|
A | G | 1 | a0001c0001t0003g0028 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.727-409A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670982 | ||||||
chr16:4670992
|
C | T | 159 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(156): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.727-399C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670992 | ||||||
chr16:4671024
|
A | C | 162 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.727-367A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4671024 | ||||||
chr16:4671119
|
C | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.727-272C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4671119 | ||||||
chr16:4671126
|
G | A | 5 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.727-265G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4671126 | ||||||
chr16:4671173
|
G | A | 2 | a0001c0001t0015g0114a0001c0001t0015g0117 | 2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.727-218G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4671173 | ||||||
chr16:4671218
|
TG | T | 4 | a0001c0001t0006g0157a0001c0001t0048g0177a0001c0001t0049g0196others(1): Show | 4 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.727-168delG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4671218 | |||||
chr16:4671258
|
C | T | 8 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0004g0057others(5): Show | 8 | HG00621.hp2 HG02027.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.727-133C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4671258 | ||||||
chr16:4671276
|
C | G | 6 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.727-115C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4671276 | ||||||
chr16:4671287
|
T | G | 7 | a0001c0001t0004g0011a0001c0001t0023g0006a0001c0001t0027g0045others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.727-104T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4671287 | ||||||
chr16:4671352
|
A | G | 3 | a0001c0001t0004g0011a0001c0001t0023g0006a0001c0001t0029g0334 | 3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.727-39A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4671352 | ||||||
chr16:4671467
|
T | C | 170 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
splice_region_variant&intron_variant | LOW | c.795+8T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671467 | ||||||
chr16:4671537
|
G | A | 2 | a0001c0001t0002g0214a0001c0001t0002g0215 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.795+78G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671537 | ||||||
chr16:4671582
|
ACAT | A | 68 | a0001c0001t0001g0318a0001c0001t0001g0320a0001c0001t0001g0327others(65): Show | 68 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.795+127_795+129del others(3): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 4671582 | |||||
chr16:4671589
|
T | C | 1 | a0001c0001t0006g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.795+130T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671589 | ||||||
chr16:4671654
|
C | G | 1 | a0001c0001t0001g0270 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.795+195C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671654 | ||||||
chr16:4671692
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.795+233G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671692 | ||||||
chr16:4671739
|
G | T | 1 | a0001c0001t0006g0252 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.795+280G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671739 | ||||||
chr16:4671755
|
C | T | 2 | a0001c0001t0002g0171a0001c0001t0007g0254 | 2 | HG00544.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.795+296C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671755 | ||||||
chr16:4671757
|
G | T | 2 | a0001c0001t0006g0154a0001c0001t0059g0135 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.795+298G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671757 | ||||||
chr16:4671764
|
C | G | 1 | a0001c0001t0002g0240 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.795+305C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671764 | ||||||
chr16:4671770
|
TC | T | 4 | a0001c0001t0005g0036a0001c0001t0005g0038a0001c0001t0005g0039others(1): Show | 4 | HG02451.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.795+315delC | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 4671770 | |||||
chr16:4671779
|
A | G | 1 | a0001c0001t0003g0060 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.795+320A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671779 | ||||||
chr16:4671839
|
T | C | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.795+380T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671839 | ||||||
chr16:4671884
|
T | C | 3 | a0001c0001t0001g0178a0001c0001t0001g0328a0001c0001t0010g0332 | 3 | HG02165.hp2 NA18966.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.795+425T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671884 | ||||||
chr16:4671932
|
G | C | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.795+473G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671932 | ||||||
chr16:4672054
|
C | T | 1 | a0001c0001t0002g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.795+595C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672054 | ||||||
chr16:4672067
|
G | A | 1 | a0001c0001t0004g0063 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.795+608G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672067 | ||||||
chr16:4672106
|
A | G | 1 | a0001c0001t0042g0189 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.795+647A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672106 | ||||||
chr16:4672156
|
G | A | 1 | a0001c0001t0023g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.795+697G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672156 | ||||||
chr16:4672166
|
A | G | 1 | a0001c0001t0002g0313 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.795+707A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672166 | ||||||
chr16:4672184
|
G | T | 3 | a0001c0001t0002g0282a0001c0001t0002g0314a0001c0001t0007g0303 | 3 | HG00597.hp1 HG02027.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.795+725G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672184 | ||||||
chr16:4672196
|
G | A | 1 | a0001c0001t0002g0276 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.795+737G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672196 | ||||||
chr16:4672200
|
A | G | 163 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.795+741A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672200 | ||||||
chr16:4672203
|
C | A | 2 | a0001c0001t0020g0012a0001c0001t0021g0042 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.795+744C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672203 | ||||||
chr16:4672381
|
G | A | 1 | a0001c0001t0029g0334 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.795+922G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672381 | ||||||
chr16:4672405
|
T | C | 2 | a0001c0001t0003g0027a0001c0001t0003g0034 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.795+946T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672405 | ||||||
chr16:4672491
|
G | C | 11 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(8): Show | 11 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.796-1007G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672491 | ||||||
chr16:4672591
|
G | A | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.796-907G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672591 | ||||||
chr16:4673016
|
T | G | 1 | a0001c0001t0023g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.796-482T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4673016 | ||||||
chr16:4673096
|
C | T | 1 | a0001c0001t0025g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.796-402C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4673096 | ||||||
chr16:4673180
|
A | C | 1 | a0001c0001t0053g0322 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.796-318A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4673180 | ||||||
chr16:4673450
|
A | G | 160 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.796-48A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4673450 | ||||||
chr16:4673748
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.955+91C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673748 | ||||||
chr16:4673758
|
T | G | 1 | a0001c0001t0002g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.955+101T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673758 | ||||||
chr16:4673775
|
C | G | 1 | a0001c0001t0058g0329 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.955+118C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673775 | ||||||
chr16:4673816
|
G | A | 3 | a0001c0001t0002g0197a0001c0001t0002g0214a0001c0001t0002g0215 | 3 | HG01106.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.955+159G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673816 | ||||||
chr16:4673816
|
G | C | 1 | a0001c0001t0011g0291 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.955+159G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673816 | ||||||
chr16:4673823
|
G | C | 2 | a0001c0003t0038g0018a0001c0004t0036g0087 | 2 | HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.955+166G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673823 | ||||||
chr16:4673834
|
A | G | 1 | a0001c0001t0002g0236 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.955+177A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673834 | ||||||
chr16:4673869
|
T | A | 3 | a0001c0001t0002g0198a0001c0001t0002g0232a0001c0001t0011g0127 | 3 | NA18942.hp2 NA18995.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.955+212T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673869 | ||||||
chr16:4673902
|
C | T | 3 | a0001c0001t0002g0197a0001c0001t0002g0214a0001c0001t0002g0215 | 3 | HG01106.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.955+245C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673902 | ||||||
chr16:4673910
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.955+253A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673910 | ||||||
chr16:4673977
|
CTTATTTT others(4): Show |
C | 2 | a0001c0001t0020g0012a0001c0001t0021g0042 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.955+326_955+336del others(11): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4673977 | |||||
chr16:4674001
|
G | C | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.955+344G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674001 | ||||||
chr16:4674076
|
C | G | 2 | a0001c0001t0001g0191a0001c0001t0012g0192 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.955+419C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674076 | ||||||
chr16:4674165
|
T | G | 158 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.955+508T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674165 | ||||||
chr16:4674199
|
G | A | 1 | a0001c0001t0009g0090 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.955+542G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674199 | ||||||
chr16:4674216
|
T | TCAAGTAA others(5): Show |
1 | a0001c0001t0002g0208 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.955+561_955+572dup others(12): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674216 | |||||
chr16:4674276
|
G | A | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.955+619G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674276 | ||||||
chr16:4674320
|
G | A | 1 | a0001c0001t0046g0182 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.955+663G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674320 | ||||||
chr16:4674337
|
G | A | 3 | a0001c0001t0025g0031a0001c0003t0038g0018a0001c0004t0036g0087 | 3 | HG02809.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.955+680G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674337 | ||||||
chr16:4674353
|
G | A | 152 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(149): Show | 152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.955+696G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674353 | ||||||
chr16:4674370
|
A | C | 2 | a0001c0001t0020g0012a0001c0001t0021g0042 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.955+713A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674370 | ||||||
chr16:4674370
|
A | G | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.955+713A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674370 | ||||||
chr16:4674522
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0168a0001c0001t0044g0139 | 3 | NA18978.hp2 NA18999.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.955+865C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674522 | ||||||
chr16:4674567
|
G | T | 4 | a0001c0001t0001g0118a0001c0001t0001g0144a0001c0001t0001g0191others(1): Show | 4 | HG01175.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.955+910G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674567 | ||||||
chr16:4674578
|
C | CT | 7 | a0001c0001t0001g0222a0001c0001t0011g0301a0001c0001t0023g0006others(4): Show | 7 | HG02809.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.955+933dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674578 | |||||
chr16:4674581
|
TTTTTTTT others(13): Show |
T | 1 | a0001c0001t0003g0066 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.955+949_955+968del others(20): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674581 | |||||
chr16:4674586
|
T | TTTTTTTC others(5): Show |
1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.955+933_955+934ins others(12): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674586 | |||||
chr16:4674587
|
TTTTCTTT others(7): Show |
T | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.955+934_955+947del others(14): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674587 | |||||
chr16:4674596
|
CTTTTCTT others(3): Show |
C | 2 | a0001c0001t0002g0149a0001c0001t0002g0289 | 2 | HG03491.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.955+949_955+958del others(10): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674596 | |||||
chr16:4674601
|
C | CT | 30 | a0001c0001t0001g0103a0001c0001t0001g0111a0001c0001t0001g0128others(27): Show | 30 | HG00140.hp1 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.955+953dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674601 | |||||
chr16:4674601
|
CTTTTTTT others(21): Show |
C | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.955+954_955+981del others(28): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674601 | |||||
chr16:4674602
|
T | TTTTTTTT others(17): Show |
1 | a0001c0001t0001g0183 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.955+958_955+959ins others(24): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674602 | |||||
chr16:4674606
|
T | C | 2 | a0001c0001t0004g0011a0001c0001t0032g0002 | 2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.955+949T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674606 | ||||||
chr16:4674611
|
C | T | 1 | a0001c0001t0014g0019 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.955+954C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674611 | ||||||
chr16:4674616
|
C | A | 5 | a0001c0001t0001g0247a0001c0001t0001g0330a0001c0001t0001g0331others(2): Show | 5 | HG00408.hp2 HG00621.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.955+959C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674616 | ||||||
chr16:4674616
|
CTTTTCTT others(4): Show |
C | 1 | a0001c0001t0002g0253 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.955+964_955+974del others(11): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674616 | |||||
chr16:4674626
|
C | CT | 126 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.955+994dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674626 | |||||
chr16:4674626
|
C | CTT | 35 | a0001c0001t0001g0108a0001c0001t0001g0122a0001c0001t0001g0136others(32): Show | 35 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.955+993_955+994dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674626 | |||||
chr16:4674626
|
C | CTTTTTTT others(19): Show |
4 | a0001c0001t0001g0247a0001c0001t0001g0330a0001c0001t0006g0125others(1): Show | 4 | HG00408.hp2 HG01928.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.955+978_955+979ins others(26): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674626 | |||||
chr16:4674626
|
C | CTTTTTTT others(20): Show |
2 | a0001c0001t0001g0331a0004c0005t0001g0162 | 2 | HG00621.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.955+978_955+979ins others(27): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674626 | |||||
chr16:4674626
|
C | T | 2 | a0001c0001t0004g0011a0001c0001t0023g0006 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.955+969C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674626 | ||||||
chr16:4674631
|
T | C | 9 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(6): Show | 9 | HG01106.hp2 HG01257.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.955+974T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674631 | ||||||
chr16:4674634
|
T | C | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.955+977T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674634 | ||||||
chr16:4674636
|
T | C | 1 | a0001c0001t0020g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.955+979T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674636 | ||||||
chr16:4674664
|
C | T | 113 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.955+1007C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674664 | ||||||
chr16:4674786
|
G | A | 18 | a0001c0001t0001g0122a0001c0001t0001g0128a0001c0001t0001g0222others(15): Show | 18 | HG00621.hp2 HG02027.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.955+1129G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674786 | ||||||
chr16:4674790
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.955+1133G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674790 | ||||||
chr16:4674796
|
G | A | 3 | a0001c0001t0003g0013a0001c0001t0004g0080a0001c0001t0022g0014 | 3 | HG02723.hp2 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.955+1139G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674796 | ||||||
chr16:4674825
|
A | G | 4 | a0001c0001t0004g0011a0001c0001t0023g0006a0001c0001t0027g0045others(1): Show | 4 | HG01243.hp1 HG02922.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.955+1168A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674825 | ||||||
chr16:4674831
|
G | A | 2 | a0001c0001t0020g0012a0001c0001t0021g0042 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.955+1174G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674831 | ||||||
chr16:4674947
|
C | T | 1 | a0001c0001t0001g0328 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.955+1290C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674947 | ||||||
chr16:4675393
|
C | T | 13 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0038others(10): Show | 13 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.955+1736C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675393 | ||||||
chr16:4675449
|
T | C | 155 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.955+1792T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675449 | ||||||
chr16:4675610
|
A | G | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-1853A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675610 | ||||||
chr16:4675650
|
G | C | 2 | a0001c0001t0023g0006a0001c0001t0029g0334 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.956-1813G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675650 | ||||||
chr16:4675653
|
C | G | 2 | a0001c0001t0007g0148a0001c0001t0007g0167 | 2 | HG01074.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.956-1810C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675653 | ||||||
chr16:4675698
|
C | A | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-1765C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675698 | ||||||
chr16:4675733
|
C | CA | 7 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0204others(4): Show | 7 | HG00735.hp2 HG02074.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.956-1713dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4675733 | |||||
chr16:4675735
|
A | G | 2 | a0001c0001t0020g0012a0001c0001t0021g0042 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.956-1728A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675735 | ||||||
chr16:4675817
|
A | G | 4 | a0001c0001t0004g0057a0001c0001t0004g0062a0001c0001t0004g0063others(1): Show | 4 | HG02027.hp2 NA18967.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-1646A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675817 | ||||||
chr16:4675843
|
A | G | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-1620A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675843 | ||||||
chr16:4675857
|
G | T | 2 | a0001c0001t0002g0237a0001c0001t0060g0238 | 2 | HG00741.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.956-1606G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675857 | ||||||
chr16:4675862
|
C | T | 130 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.956-1601C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675862 | ||||||
chr16:4675900
|
T | C | 1 | a0001c0001t0009g0076 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.956-1563T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675900 | ||||||
chr16:4675910
|
G | A | 2 | a0001c0001t0023g0006a0001c0001t0029g0334 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.956-1553G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675910 | ||||||
chr16:4675919
|
C | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-1544C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675919 | ||||||
chr16:4676001
|
C | T | 2 | a0001c0001t0023g0006a0001c0001t0029g0334 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.956-1462C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676001 | ||||||
chr16:4676007
|
A | G | 167 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.956-1456A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676007 | ||||||
chr16:4676045
|
C | G | 3 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0008g0022 | 3 | HG02486.hp2 HG02896.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.956-1418C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676045 | ||||||
chr16:4676102
|
C | A | 6 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.956-1361C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676102 | ||||||
chr16:4676227
|
G | A | 1 | a0001c0001t0019g0010 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.956-1236G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676227 | ||||||
chr16:4676374
|
T | A | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-1089T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676374 | ||||||
chr16:4676450
|
C | G | 151 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.956-1013C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676450 | ||||||
chr16:4676466
|
G | T | 1 | a0001c0001t0003g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.956-997G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676466 | ||||||
chr16:4676470
|
G | A | 1 | a0001c0001t0006g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.956-993G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676470 | ||||||
chr16:4676477
|
C | T | 2 | a0001c0001t0020g0012a0001c0001t0021g0042 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.956-986C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676477 | ||||||
chr16:4676556
|
C | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-907C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676556 | ||||||
chr16:4676578
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.956-885C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676578 | ||||||
chr16:4676611
|
C | G | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.956-852C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676611 | ||||||
chr16:4676612
|
T | A | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-851T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676612 | ||||||
chr16:4676626
|
C | G | 2 | a0001c0001t0004g0011a0001c0001t0032g0002 | 2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.956-837C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676626 | ||||||
chr16:4676635
|
C | A | 1 | a0001c0001t0001g0245 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.956-828C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676635 | ||||||
chr16:4676636
|
A | G | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-827A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676636 | ||||||
chr16:4676703
|
A | C | 1 | a0001c0001t0003g0060 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.956-760A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676703 | ||||||
chr16:4676805
|
C | G | 1 | a0001c0001t0003g0030 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.956-658C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676805 | ||||||
chr16:4676837
|
G | A | 2 | a0001c0001t0025g0031a0001c0004t0036g0087 | 2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.956-626G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676837 | ||||||
chr16:4676848
|
G | A | 1 | a0001c0001t0008g0026 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.956-615G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676848 | ||||||
chr16:4676875
|
C | T | 1 | a0001c0001t0011g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.956-588C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676875 | ||||||
chr16:4676876
|
G | A | 1 | a0001c0003t0038g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.956-587G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676876 | ||||||
chr16:4676970
|
G | A | 2 | a0001c0001t0001g0244a0001c0001t0002g0142 | 2 | HG01952.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.956-493G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676970 | ||||||
chr16:4676975
|
C | T | 14 | a0001c0001t0005g0032a0001c0001t0005g0091a0001c0001t0008g0100others(11): Show | 14 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.956-488C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676975 | ||||||
chr16:4677037
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.956-426G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677037 | ||||||
chr16:4677047
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.956-416G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677047 | ||||||
chr16:4677075
|
A | T | 1 | a0001c0001t0030g0058 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.956-388A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677075 | ||||||
chr16:4677101
|
C | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-362C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677101 | ||||||
chr16:4677127
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.956-336G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677127 | ||||||
chr16:4677179
|
A | G | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.956-284A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677179 | ||||||
chr16:4677331
|
G | A | 2 | a0001c0001t0020g0012a0001c0001t0021g0042 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.956-132G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677331 | ||||||
chr16:4677359
|
G | A | 1 | a0001c0001t0017g0176 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.956-104G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677359 | ||||||
chr16:4677399
|
G | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-64G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677399 | ||||||
chr16:4677460
|
C | T | 1 | a0001c0003t0038g0018 | 1 | HG03195.hp2 | splice_region_variant&intron_variant | LOW | c.956-3C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677460 | ||||||
chr16:4677677
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1065+105G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677677 | ||||||
chr16:4677799
|
A | G | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1065+227A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677799 | ||||||
chr16:4677836
|
C | CT | 29 | a0001c0001t0002g0130a0001c0001t0002g0232a0001c0001t0002g0237others(26): Show | 29 | HG00408.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1065+282dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr16 | 4677836 | |||||
chr16:4677836
|
CT | C | 148 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.1065+282delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr16 | 4677836 | |||||
chr16:4677856
|
T | C | 2 | a0001c0001t0020g0012a0001c0001t0021g0042 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1065+284T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677856 | ||||||
chr16:4677884
|
C | T | 2 | a0001c0001t0025g0031a0001c0004t0036g0087 | 2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1065+312C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677884 | ||||||
chr16:4677885
|
G | A | 1 | a0001c0001t0003g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1065+313G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677885 | ||||||
chr16:4677912
|
A | T | 1 | a0001c0001t0002g0208 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1065+340A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677912 | ||||||
chr16:4677948
|
A | G | 1 | a0001c0001t0006g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1065+376A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677948 | ||||||
chr16:4677952
|
A | G | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1065+380A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677952 | ||||||
chr16:4677986
|
C | A | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1065+414C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677986 | ||||||
chr16:4677988
|
C | T | 1 | a0001c0003t0038g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1065+416C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677988 | ||||||
chr16:4677989
|
G | A | 1 | a0001c0001t0011g0301 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1065+417G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677989 | ||||||
chr16:4678165
|
A | G | 2 | a0001c0001t0020g0012a0001c0001t0021g0042 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1065+593A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678165 | ||||||
chr16:4678166
|
G | T | 2 | a0001c0001t0020g0012a0001c0001t0021g0042 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1065+594G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678166 | ||||||
chr16:4678223
|
C | T | 1 | a0001c0001t0003g0065 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1065+651C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678223 | ||||||
chr16:4678224
|
G | A | 1 | a0001c0001t0029g0334 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1065+652G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678224 | ||||||
chr16:4678287
|
A | AGG | 126 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.1065+717_1065+718d others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr16 | 4678287 | |||||
chr16:4678318
|
AAGAC | A | 3 | a0001c0001t0005g0088a0001c0001t0020g0012a0001c0001t0021g0042 | 3 | HG03098.hp1 HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1065+754_1065+757d others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr16 | 4678318 | |||||
chr16:4678357
|
A | C | 1 | a0001c0001t0001g0261 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1065+785A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678357 | ||||||
chr16:4678526
|
T | C | 152 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.1065+954T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678526 | ||||||
chr16:4678536
|
C | T | 3 | a0001c0001t0007g0148a0001c0001t0007g0167a0001c0001t0011g0152 | 3 | HG01074.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1065+964C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678536 | ||||||
chr16:4678704
|
G | A | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1065+1132G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678704 | ||||||
chr16:4678705
|
C | T | 1 | a0001c0001t0034g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1065+1133C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678705 | ||||||
chr16:4678836
|
C | G | 1 | a0001c0001t0004g0050 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1066-1196C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678836 | ||||||
chr16:4678857
|
C | T | 3 | a0001c0001t0032g0002a0001c0003t0018g0109a0001c0003t0018g0110 | 3 | HG01167.hp1 HG01169.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1066-1175C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678857 | ||||||
chr16:4678861
|
C | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1066-1171C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678861 | ||||||
chr16:4678931
|
A | T | 1 | a0001c0001t0003g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1066-1101A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678931 | ||||||
chr16:4678945
|
T | G | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1066-1087T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678945 | ||||||
chr16:4678976
|
A | G | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1066-1056A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678976 | ||||||
chr16:4679129
|
G | A | 1 | a0001c0001t0001g0331 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1066-903G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679129 | ||||||
chr16:4679142
|
G | A | 1 | a0001c0001t0003g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1066-890G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679142 | ||||||
chr16:4679319
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0224 | 2 | HG00099.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1066-713C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679319 | ||||||
chr16:4679453
|
C | T | 1 | a0001c0001t0002g0316 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1066-579C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679453 | ||||||
chr16:4679480
|
C | G | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1066-552C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679480 | ||||||
chr16:4679508
|
C | T | 1 | a0001c0003t0038g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1066-524C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679508 | ||||||
chr16:4679627
|
C | T | 1 | a0001c0001t0011g0301 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1066-405C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679627 | ||||||
chr16:4679669
|
C | A | 1 | a0001c0001t0028g0071 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1066-363C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679669 | ||||||
chr16:4679680
|
C | T | 1 | a0001c0001t0028g0071 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1066-352C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679680 | ||||||
chr16:4679680
|
CCCTGCAC others(4): Show |
C | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1066-345_1066-335d others(13): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr16 | 4679680 | |||||
chr16:4679769
|
G | A | 1 | a0001c0001t0011g0301 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1066-263G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679769 | ||||||
chr16:4679779
|
A | G | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1066-253A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679779 | ||||||
chr16:4679780
|
T | A | 1 | a0001c0001t0011g0301 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1066-252T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679780 | ||||||
chr16:4679781
|
G | T | 1 | a0001c0001t0011g0301 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1066-251G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679781 | ||||||
chr16:4679828
|
C | G | 1 | a0001c0003t0038g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1066-204C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679828 | ||||||
chr16:4679905
|
G | A | 1 | a0001c0001t0060g0238 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1066-127G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679905 | ||||||
chr16:4679910
|
C | T | 1 | a0001c0003t0038g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1066-122C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679910 | ||||||
chr16:4679991
|
G | C | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1066-41G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679991 | ||||||
chr16:4680134
|
C | G | 1 | a0001c0001t0058g0329 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1131+37C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680134 | ||||||
chr16:4680135
|
C | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1131+38C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680135 | ||||||
chr16:4680172
|
C | G | 1 | a0001c0001t0001g0206 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1131+75C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680172 | ||||||
chr16:4680201
|
A | C | 4 | a0001c0001t0002g0174a0001c0001t0002g0313a0001c0001t0013g0288others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1131+104A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680201 | ||||||
chr16:4680233
|
G | A | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1131+136G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680233 | ||||||
chr16:4680263
|
G | A | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1131+166G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680263 | ||||||
chr16:4680269
|
G | T | 1 | a0001c0001t0001g0206 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1131+172G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680269 | ||||||
chr16:4680325
|
C | G | 2 | a0001c0001t0013g0194a0001c0001t0016g0054 | 2 | HG01515.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1131+228C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680325 | ||||||
chr16:4680397
|
A | G | 1 | a0001c0001t0013g0194 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1131+300A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680397 | ||||||
chr16:4680419
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1131+322G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680419 | ||||||
chr16:4680464
|
C | T | 2 | a0001c0001t0002g0242a0001c0001t0003g0061 | 2 | HG02083.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1131+367C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680464 | ||||||
chr16:4680576
|
C | T | 1 | a0001c0006t0009g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1131+479C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680576 | ||||||
chr16:4680578
|
C | T | 1 | a0001c0001t0005g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1131+481C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680578 | ||||||
chr16:4680579
|
C | T | 3 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0069 | 3 | HG00099.hp2 HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1131+482C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680579 | ||||||
chr16:4680685
|
A | T | 1 | a0001c0001t0025g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1131+588A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680685 | ||||||
chr16:4680790
|
C | T | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1131+693C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680790 | ||||||
chr16:4680791
|
G | A | 1 | a0001c0001t0058g0329 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1131+694G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680791 | ||||||
chr16:4680869
|
C | G | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1132-681C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680869 | ||||||
chr16:4680979
|
C | T | 1 | a0001c0001t0025g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1132-571C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680979 | ||||||
chr16:4681128
|
C | T | 3 | a0001c0001t0014g0019a0001c0001t0014g0020a0001c0001t0033g0021 | 3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1132-422C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681128 | ||||||
chr16:4681154
|
G | A | 150 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(147): Show | 150 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1132-396G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681154 | ||||||
chr16:4681181
|
C | T | 1 | a0001c0001t0006g0309 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1132-369C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681181 | ||||||
chr16:4681253
|
G | A | 1 | a0003c0007t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1132-297G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681253 | ||||||
chr16:4681296
|
G | T | 1 | a0001c0001t0013g0194 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1132-254G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681296 | ||||||
chr16:4681335
|
C | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1132-215C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681335 | ||||||
chr16:4681375
|
C | A | 1 | a0001c0001t0002g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1132-175C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681375 | ||||||
chr16:4681400
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1132-150C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681400 | ||||||
chr16:4681493
|
G | A | 5 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1132-57G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681493 | ||||||
chr16:4681532
|
C | T | 5 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1132-18C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681532 | ||||||
chr16:4681907
|
C | T | 1 | a0001c0001t0007g0148 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1358+131C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4681907 | ||||||
chr16:4681928
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1358+152G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4681928 | ||||||
chr16:4681975
|
G | A | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1358+199G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4681975 | ||||||
chr16:4681978
|
C | T | 1 | a0001c0001t0003g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1358+202C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4681978 | ||||||
chr16:4682009
|
G | C | 1 | a0001c0001t0001g0122 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1358+233G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682009 | ||||||
chr16:4682121
|
T | C | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1358+345T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682121 | ||||||
chr16:4682156
|
G | A | 1 | a0001c0001t0002g0273 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1358+380G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682156 | ||||||
chr16:4682180
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1358+404A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682180 | ||||||
chr16:4682223
|
C | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1358+447C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682223 | ||||||
chr16:4682244
|
C | T | 3 | a0001c0001t0014g0019a0001c0001t0014g0020a0001c0001t0033g0021 | 3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1358+468C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682244 | ||||||
chr16:4682326
|
C | T | 2 | a0001c0001t0042g0189a0001c0001t0043g0190 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1359-497C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682326 | ||||||
chr16:4682356
|
C | T | 6 | a0001c0001t0001g0136a0001c0001t0001g0168a0001c0001t0001g0207others(3): Show | 6 | NA18977.hp2 NA18978.hp2 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.1359-467C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682356 | ||||||
chr16:4682507
|
G | A | 1 | a0001c0001t0005g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1359-316G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682507 | ||||||
chr16:4682598
|
G | C | 3 | a0001c0001t0003g0029a0001c0001t0003g0030a0001c0001t0003g0033 | 3 | HG02280.hp2 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1359-225G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682598 | ||||||
chr16:4682600
|
G | GTGTCGGG others(8): Show |
1 | a0001c0001t0016g0054 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1359-215_1359-201d others(17): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr16 | 4682600 | |||||
chr16:4682957
|
C | G | 2 | a0001c0001t0007g0274a0001c0001t0007g0292 | 2 | HG02155.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1482+11C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 14/16 | chr16 | 4682957 | ||||||
chr16:4682978
|
C | T | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1482+32C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 14/16 | chr16 | 4682978 | ||||||
chr16:4682989
|
G | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1482+43G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 14/16 | chr16 | 4682989 | ||||||
chr16:4683055
|
T | C | 1 | a0001c0001t0013g0288 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1482+109T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 14/16 | chr16 | 4683055 | ||||||
chr16:4683068
|
C | G | 1 | a0001c0006t0009g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1482+122C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 14/16 | chr16 | 4683068 | ||||||
chr16:4683076
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1482+130C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 14/16 | chr16 | 4683076 | ||||||
chr16:4683281
|
C | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1528+12C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683281 | ||||||
chr16:4683310
|
C | T | 3 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0326 | 3 | HG01074.hp2 HG01109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1528+41C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683310 | ||||||
chr16:4683326
|
T | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0284 | 2 | NA19065.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1528+57T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683326 | ||||||
chr16:4683344
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0212 | 2 | HG00735.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1528+75C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683344 | ||||||
chr16:4683375
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1528+106C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683375 | ||||||
chr16:4683422
|
C | T | 1 | a0001c0001t0003g0066 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1528+153C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683422 | ||||||
chr16:4683537
|
C | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1528+268C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683537 | ||||||
chr16:4683541
|
T | G | 156 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1528+272T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683541 | ||||||
chr16:4683551
|
A | T | 3 | a0001c0001t0023g0006a0001c0001t0029g0334a0001c0001t0032g0002 | 3 | HG01884.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1528+282A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683551 | ||||||
chr16:4683556
|
CA | C | 158 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(155): Show | 158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.1529-275delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr16 | 4683556 | |||||
chr16:4683700
|
G | A | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1529-143G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683700 | ||||||
chr16:4683946
|
G | A | 1 | a0001c0003t0038g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1618+14G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4683946 | ||||||
chr16:4684184
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1618+252G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684184 | ||||||
chr16:4684270
|
C | T | 3 | a0001c0001t0001g0118a0001c0001t0001g0191a0001c0001t0012g0192 | 3 | HG03490.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1618+338C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684270 | ||||||
chr16:4684271
|
G | A | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1618+339G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684271 | ||||||
chr16:4684310
|
G | C | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1618+378G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684310 | ||||||
chr16:4684332
|
C | T | 2 | a0001c0001t0003g0027a0001c0001t0003g0034 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1618+400C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684332 | ||||||
chr16:4684391
|
G | A | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1618+459G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684391 | ||||||
chr16:4684414
|
C | T | 5 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618+482C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684414 | ||||||
chr16:4684419
|
G | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1618+487G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684419 | ||||||
chr16:4684428
|
G | C | 3 | a0001c0001t0009g0075a0001c0001t0009g0076a0001c0001t0025g0031 | 3 | HG03209.hp1 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1618+496G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684428 | ||||||
chr16:4684464
|
G | A | 5 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618+532G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684464 | ||||||
chr16:4684512
|
C | T | 147 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(144): Show | 147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1618+580C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684512 | ||||||
chr16:4684546
|
C | T | 3 | a0001c0001t0023g0006a0001c0001t0029g0334a0001c0001t0032g0002 | 3 | HG01884.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1618+614C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684546 | ||||||
chr16:4684552
|
C | T | 5 | a0001c0001t0008g0023a0001c0001t0008g0024a0001c0001t0008g0025others(2): Show | 5 | HG02559.hp2 HG02615.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618+620C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684552 | ||||||
chr16:4684578
|
G | A | 1 | a0001c0001t0010g0332 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1618+646G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684578 | ||||||
chr16:4684589
|
T | C | 301 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(298): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1618+657T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684589 | ||||||
chr16:4684631
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1618+699G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684631 | ||||||
chr16:4684694
|
C | G | 1 | a0001c0001t0001g0128 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1618+762C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684694 | ||||||
chr16:4684705
|
C | T | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1618+773C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684705 | ||||||
chr16:4684726
|
G | C | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1618+794G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684726 | ||||||
chr16:4684743
|
T | C | 1 | a0001c0001t0003g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1618+811T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684743 | ||||||
chr16:4684786
|
C | G | 3 | a0001c0001t0023g0006a0001c0001t0029g0334a0001c0001t0032g0002 | 3 | HG01884.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1618+854C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684786 | ||||||
chr16:4684944
|
G | T | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1618+1012G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684944 | ||||||
chr16:4685004
|
AGTGGCCT others(6): Show |
A | 2 | a0001c0001t0001g0268a0001c0001t0006g0269 | 2 | NA19064.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1618+1073_1618+108 others(17): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685004 | ||||||
chr16:4685186
|
T | G | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1618+1254T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685186 | ||||||
chr16:4685264
|
T | C | 4 | a0001c0001t0023g0006a0001c0001t0025g0031a0001c0001t0029g0334others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+1332T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685264 | ||||||
chr16:4685299
|
TCTCAGAG others(12): Show |
T | 1 | a0001c0001t0013g0186 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1618+1371_1618+138 others(23): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4685299 | |||||
chr16:4685385
|
C | T | 1 | a0001c0001t0006g0309 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1618+1453C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685385 | ||||||
chr16:4685499
|
C | T | 1 | a0001c0001t0011g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1618+1567C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685499 | ||||||
chr16:4685527
|
C | T | 154 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1618+1595C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685527 | ||||||
chr16:4685552
|
T | C | 1 | a0001c0001t0001g0328 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1618+1620T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685552 | ||||||
chr16:4685630
|
T | C | 1 | a0001c0004t0036g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1618+1698T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685630 | ||||||
chr16:4685630
|
T | G | 157 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1618+1698T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685630 | ||||||
chr16:4685633
|
G | A | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1618+1701G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685633 | ||||||
chr16:4685643
|
C | T | 10 | a0001c0001t0001g0163a0001c0001t0001g0183a0001c0001t0001g0206others(7): Show | 10 | HG01070.hp2 HG01258.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1618+1711C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685643 | ||||||
chr16:4685702
|
C | G | 1 | a0001c0001t0007g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1618+1770C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685702 | ||||||
chr16:4685904
|
C | G | 3 | a0001c0001t0002g0153a0001c0001t0002g0250a0001c0001t0052g0169 | 3 | NA18964.hp2 NA18975.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1618+1972C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685904 | ||||||
chr16:4685948
|
C | G | 1 | a0001c0001t0025g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1618+2016C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685948 | ||||||
chr16:4686018
|
G | T | 1 | a0001c0001t0002g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1618+2086G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686018 | ||||||
chr16:4686063
|
G | A | 1 | a0001c0001t0025g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1618+2131G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686063 | ||||||
chr16:4686079
|
TTCTGGCT others(4): Show |
T | 133 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.1618+2152_1618+216 others(15): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4686079 | |||||
chr16:4686096
|
C | T | 1 | a0001c0001t0013g0194 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1618+2164C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686096 | ||||||
chr16:4686114
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1618+2182C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686114 | ||||||
chr16:4686214
|
G | C | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1618+2282G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686214 | ||||||
chr16:4686224
|
C | G | 1 | a0001c0001t0002g0202 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1618+2292C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686224 | ||||||
chr16:4686250
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1618+2318T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686250 | ||||||
chr16:4686315
|
C | T | 162 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1618+2383C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686315 | ||||||
chr16:4686365
|
T | A | 1 | a0001c0001t0001g0181 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1619-2431T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686365 | ||||||
chr16:4686419
|
G | A | 6 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1619-2377G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686419 | ||||||
chr16:4686531
|
C | T | 1 | a0001c0001t0024g0085 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1619-2265C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686531 | ||||||
chr16:4686694
|
C | A | 1 | a0001c0001t0003g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1619-2102C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686694 | ||||||
chr16:4686716
|
G | A | 4 | a0001c0001t0001g0111a0001c0001t0002g0153a0001c0001t0002g0250others(1): Show | 4 | HG02683.hp1 NA18964.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-2080G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686716 | ||||||
chr16:4686822
|
G | A | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1619-1974G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686822 | ||||||
chr16:4686833
|
G | A | 158 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.1619-1963G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686833 | ||||||
chr16:4687016
|
C | T | 1 | a0001c0001t0025g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1619-1780C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687016 | ||||||
chr16:4687134
|
C | T | 3 | a0001c0001t0020g0012a0001c0001t0021g0042a0001c0003t0038g0018 | 3 | HG03098.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1619-1662C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687134 | ||||||
chr16:4687207
|
T | TC | 154 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1619-1582dupC | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687207 | |||||
chr16:4687221
|
C | T | 6 | a0001c0001t0006g0132a0001c0001t0006g0133a0001c0001t0006g0157others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1619-1575C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687221 | ||||||
chr16:4687299
|
C | T | 1 | a0001c0001t0005g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1619-1497C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687299 | ||||||
chr16:4687312
|
G | A | 3 | a0001c0001t0020g0012a0001c0001t0021g0042a0001c0003t0038g0018 | 3 | HG03098.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1619-1484G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687312 | ||||||
chr16:4687364
|
C | G | 2 | a0001c0001t0003g0013a0001c0001t0022g0014 | 2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1619-1432C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687364 | ||||||
chr16:4687382
|
G | A | 155 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.1619-1414G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687382 | ||||||
chr16:4687405
|
C | T | 1 | a0001c0001t0006g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1619-1391C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687405 | ||||||
chr16:4687463
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1619-1333C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687463 | ||||||
chr16:4687528
|
A | C | 16 | a0001c0001t0004g0089a0001c0001t0005g0032a0001c0001t0005g0091others(13): Show | 16 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1619-1268A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687528 | ||||||
chr16:4687534
|
A | C | 1 | a0001c0001t0050g0251 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1619-1262A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687534 | ||||||
chr16:4687578
|
T | TAC | 26 | a0001c0001t0001g0204a0001c0001t0001g0212a0001c0001t0002g0141others(23): Show | 26 | HG00544.hp1 HG00673.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1619-1189_1619-118 others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | |||||
chr16:4687578
|
T | TACAC | 6 | a0001c0001t0002g0184a0001c0001t0002g0279a0001c0001t0002g0280others(3): Show | 6 | HG00738.hp1 HG01081.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1619-1191_1619-118 others(8): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | |||||
chr16:4687578
|
T | TACACACA others(3): Show |
10 | a0001c0001t0001g0223a0001c0001t0001g0286a0001c0001t0005g0036others(7): Show | 10 | HG01943.hp1 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1619-1197_1619-118 others(14): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | |||||
chr16:4687578
|
T | TACACACA others(5): Show |
11 | a0001c0001t0001g0111a0001c0001t0005g0037a0001c0001t0005g0041others(8): Show | 11 | HG01891.hp2 HG02056.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1619-1199_1619-118 others(16): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | |||||
chr16:4687578
|
T | TACACACA others(7): Show |
88 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0113others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1619-1201_1619-118 others(18): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | |||||
chr16:4687578
|
T | TACACACA others(9): Show |
19 | a0001c0001t0001g0108a0001c0001t0001g0115a0001c0001t0001g0118others(16): Show | 19 | HG00099.hp1 HG00673.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.1619-1203_1619-118 others(20): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | |||||
chr16:4687578
|
T | TACACACA others(11): Show |
8 | a0001c0001t0001g0107a0001c0001t0001g0129a0001c0001t0001g0144others(5): Show | 8 | HG00280.hp2 HG00621.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.1619-1205_1619-118 others(22): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | |||||
chr16:4687578
|
T | TACACACA others(13): Show |
5 | a0001c0001t0006g0133a0001c0001t0006g0157a0001c0001t0006g0164others(2): Show | 5 | HG00280.hp1 HG00323.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1619-1207_1619-118 others(24): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | |||||
chr16:4687578
|
T | TACACACA others(15): Show |
1 | a0001c0001t0001g0270 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1619-1209_1619-118 others(26): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | |||||
chr16:4687578
|
T | TACACACA others(21): Show |
2 | a0001c0001t0006g0132a0001c0001t0006g0257 | 2 | HG01192.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1619-1215_1619-118 others(32): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | |||||
chr16:4687578
|
TAC | T | 5 | a0001c0001t0003g0029a0001c0001t0003g0030a0001c0001t0003g0033others(2): Show | 5 | HG00544.hp2 HG02083.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1619-1189_1619-118 others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | |||||
chr16:4687580
|
C | T | 1 | a0001c0001t0050g0251 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1619-1216C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687580 | ||||||
chr16:4687608
|
C | CACACACA others(8): Show |
1 | a0001c0001t0001g0137 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1619-1188_1619-118 others(19): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687608 | ||||||
chr16:4687678
|
C | G | 1 | a0001c0001t0002g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1619-1118C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687678 | ||||||
chr16:4687721
|
C | T | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1619-1075C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687721 | ||||||
chr16:4687736
|
C | T | 9 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0171others(6): Show | 9 | HG00544.hp1 HG00673.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.1619-1060C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687736 | ||||||
chr16:4687759
|
C | T | 1 | a0001c0001t0003g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1619-1037C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687759 | ||||||
chr16:4687949
|
G | A | 2 | a0001c0003t0018g0109a0001c0003t0018g0110 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1619-847G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687949 | ||||||
chr16:4687954
|
C | T | 1 | a0001c0001t0006g0269 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1619-842C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687954 | ||||||
chr16:4687975
|
G | T | 1 | a0001c0001t0002g0313 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1619-821G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687975 | ||||||
chr16:4687980
|
G | A | 117 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0108others(114): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1619-816G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687980 | ||||||
chr16:4687983
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1619-813C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687983 | ||||||
chr16:4688010
|
C | T | 1 | a0001c0001t0009g0093 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1619-786C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688010 | ||||||
chr16:4688053
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1619-743C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688053 | ||||||
chr16:4688105
|
C | T | 1 | a0001c0001t0032g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1619-691C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688105 | ||||||
chr16:4688123
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0012g0192 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1619-673C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688123 | ||||||
chr16:4688194
|
C | T | 3 | a0001c0001t0002g0197a0001c0001t0002g0214a0001c0001t0002g0215 | 3 | HG01106.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1619-602C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688194 | ||||||
chr16:4688195
|
G | A | 1 | a0001c0001t0029g0334 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1619-601G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688195 | ||||||
chr16:4688250
|
T | C | 208 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1619-546T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688250 | ||||||
chr16:4688251
|
G | C | 1 | a0001c0001t0050g0251 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1619-545G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688251 | ||||||
chr16:4688324
|
C | T | 1 | a0001c0001t0043g0190 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1619-472C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688324 | ||||||
chr16:4688330
|
A | G | 1 | a0001c0001t0027g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1619-466A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688330 | ||||||
chr16:4688386
|
C | T | 5 | a0001c0001t0001g0225a0001c0001t0004g0050a0001c0001t0048g0177others(2): Show | 5 | HG00323.hp2 HG01081.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1619-410C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688386 | ||||||
chr16:4688387
|
C | A | 3 | a0001c0001t0013g0131a0001c0001t0013g0185a0001c0001t0013g0186 | 3 | HG04184.hp2 HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1619-409C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688387 | ||||||
chr16:4688387
|
C | G | 329 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(326): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1619-409C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688387 | ||||||
chr16:4688485
|
G | A | 5 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1619-311G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688485 | ||||||
chr16:4688517
|
C | T | 1 | a0001c0001t0031g0046 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1619-279C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688517 | ||||||
chr16:4688528
|
C | T | 3 | a0001c0001t0020g0012a0001c0001t0021g0042a0001c0003t0038g0018 | 3 | HG03098.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1619-268C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688528 | ||||||
chr16:4688593
|
G | A | 1 | a0001c0001t0002g0310 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1619-203G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688593 | ||||||
chr16:4688689
|
G | C | 1 | a0001c0001t0003g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1619-107G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688689 | ||||||
chr16:4688755
|
G | T | 1 | a0001c0001t0002g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1619-41G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688755 | ||||||
chr16:4688785
|
C | T | 1 | a0001c0001t0002g0202 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1619-11C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688785 | ||||||
chr16:4688792
|
G | A | 1 | a0001c0001t0016g0070 | 1 | NA20905.hp2 | splice_region_variant&intron_variant | LOW | c.1619-4G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688792 |