geneid | 4134 |
---|---|
ensemblid | ENSG00000047849.22 |
hgncid | 6862 |
symbol | MAP4 |
name | microtubule associated protein 4 |
refseq_nuc | NM_001385682.1 |
refseq_prot | NP_001372611.1 |
ensembl_nuc | ENST00000683076.1 |
ensembl_prot | ENSP00000507895.1 |
mane_status | MANE Select |
chr | chr3 |
start | 47850695 |
end | 48016416 |
strand | - |
ver | v1.2 |
region | chr3:47850695-48016416 |
region5000 | chr3:47845695-48021416 |
regionname0 | MAP4_chr3_47850695_48016416 |
regionname5000 | MAP4_chr3_47845695_48021416 |
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 | 1/0 | 2296 | 96 | 20 | 18 | 41 | 4 | 12 | 32 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0002 | 0/1 | 2296 | 68 | 11 | 16 | 36 | 2 | 2 | 30 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0003 | 0/0 | 2296 | 13 | 12 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0004 | 0/0 | 2296 | 9 | 4 | 1 | 3 | 0 | 1 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0005 | 0/0 | 2296 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0006 | 0/0 | 2296 | 6 | 0 | 1 | 0 | 0 | 5 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0007 | 0/0 | 2296 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0008 | 0/0 | 2296 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0009 | 0/0 | 2296 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0010 | 0/0 | 2296 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0011 | 0/0 | 2296 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0012 | 0/0 | 2296 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0013 | 0/0 | 2296 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0014 | 0/0 | 2296 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0015 | 0/0 | 2296 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0016 | 0/0 | 2296 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0017 | 0/0 | 2296 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0018 | 0/0 | 2296 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0019 | 0/0 | 2296 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0020 | 0/0 | 2296 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0021 | 0/0 | 2296 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0022 | 0/0 | 2296 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0023 | 0/0 | 2296 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0024 | 0/0 | 2296 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0025 | 0/0 | 2296 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0026 | 0/0 | 2296 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0027 | 0/0 | 2296 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0028 | 0/0 | 2296 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
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 | 6891 | 91 | 16 | 18 | 41 | 3 | 12 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0002 | 0/1 | 6891 | 65 | 10 | 14 | 36 | 2 | 2 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0003 | 0/0 | 6891 | 13 | 12 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0004 | 0/0 | 6891 | 9 | 4 | 1 | 3 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0005 | 0/0 | 6891 | 7 | 7 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0006 | 0/0 | 6891 | 6 | 0 | 1 | 0 | 0 | 5 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0007 | 0/0 | 6891 | 4 | 4 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0008 | 0/0 | 6891 | 4 | 4 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0009 | 0/0 | 6891 | 3 | 3 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0010 | 0/0 | 6891 | 3 | 2 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0011 | 0/0 | 6891 | 2 | 0 | 2 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0012 | 0/0 | 6891 | 2 | 0 | 0 | 0 | 0 | 2 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0013 | 0/0 | 6891 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0014 | 0/0 | 6891 | 2 | 0 | 0 | 2 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0015 | 0/0 | 6891 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0016 | 0/0 | 6891 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0017 | 0/0 | 6891 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0018 | 0/0 | 6891 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0019 | 0/0 | 6891 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0020 | 0/0 | 6891 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0021 | 0/0 | 6891 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0022 | 0/0 | 6891 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0023 | 0/0 | 6891 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0024 | 0/0 | 6891 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0025 | 0/0 | 6891 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0026 | 0/0 | 6891 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0027 | 0/0 | 6891 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0028 | 0/0 | 6891 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0029 | 0/0 | 6891 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0030 | 0/0 | 6891 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0031 | 0/0 | 6891 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
c0032 | 0/0 | 6891 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2342 | 91 | 14 | 18 | 43 | 4 | 11 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0002 | 0/1 | 2345 | 73 | 16 | 17 | 28 | 2 | 9 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0003 | 0/0 | 2345 | 21 | 20 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0004 | 0/0 | 2345 | 9 | 0 | 0 | 9 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0005 | 0/0 | 2345 | 5 | 0 | 0 | 4 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0006 | 0/0 | 2345 | 4 | 1 | 3 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0007 | 0/0 | 2345 | 4 | 4 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0008 | 0/0 | 2345 | 3 | 2 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0009 | 0/0 | 2342 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0010 | 0/0 | 2345 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0011 | 0/0 | 2345 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0012 | 0/0 | 2345 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0013 | 0/0 | 2342 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0014 | 0/0 | 2345 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0015 | 0/0 | 2342 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0016 | 0/0 | 2342 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0017 | 0/0 | 2342 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0018 | 0/0 | 2344 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0019 | 0/0 | 2344 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0020 | 0/0 | 2345 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0021 | 0/0 | 2345 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0022 | 0/0 | 2345 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0023 | 0/0 | 2345 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0024 | 0/0 | 2342 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0025 | 0/0 | 2344 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
t0026 | 0/0 | 2342 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
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 | 6891 | 91 | 16 | 18 | 41 | 3 | 12 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0001c0007 | 0/0 | 6891 | 4 | 4 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0001c0024 | 0/0 | 6891 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0002c0002 | 0/1 | 6891 | 65 | 10 | 14 | 36 | 2 | 2 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0002c0011 | 0/0 | 6891 | 2 | 0 | 2 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0002c0020 | 0/0 | 6891 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0003c0003 | 0/0 | 6891 | 13 | 12 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0004c0004 | 0/0 | 6891 | 9 | 4 | 1 | 3 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0005c0005 | 0/0 | 6891 | 7 | 7 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0006c0006 | 0/0 | 6891 | 6 | 0 | 1 | 0 | 0 | 5 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0007c0008 | 0/0 | 6891 | 4 | 4 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0008c0010 | 0/0 | 6891 | 3 | 2 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0009c0009 | 0/0 | 6891 | 3 | 3 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0010c0015 | 0/0 | 6891 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0011c0014 | 0/0 | 6891 | 2 | 0 | 0 | 2 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0012c0013 | 0/0 | 6891 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0013c0012 | 0/0 | 6891 | 2 | 0 | 0 | 0 | 0 | 2 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0014c0032 | 0/0 | 6891 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0015c0030 | 0/0 | 6891 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0016c0029 | 0/0 | 6891 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0017c0028 | 0/0 | 6891 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0018c0023 | 0/0 | 6891 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0019c0031 | 0/0 | 6891 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0020c0022 | 0/0 | 6891 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0021c0025 | 0/0 | 6891 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0022c0026 | 0/0 | 6891 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0023c0027 | 0/0 | 6891 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0024c0019 | 0/0 | 6891 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0025c0018 | 0/0 | 6891 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0026c0017 | 0/0 | 6891 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0027c0021 | 0/0 | 6891 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0028c0016 | 0/0 | 6891 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 9232 | 82 | 10 | 17 | 40 | 3 | 11 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0001c0001t0002 | 0/0 | 9235 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0001c0001t0009 | 0/0 | 9232 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0001c0001t0010 | 0/0 | 9235 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0001c0001t0013 | 0/0 | 9232 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0001c0001t0017 | 0/0 | 9232 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0001c0001t0024 | 0/0 | 9232 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0001c0001t0026 | 0/0 | 9232 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0001c0007t0001 | 0/0 | 9232 | 4 | 4 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0001c0024t0001 | 0/0 | 9232 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0002c0002t0002 | 0/1 | 9235 | 51 | 9 | 12 | 26 | 2 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0002c0002t0004 | 0/0 | 9235 | 9 | 0 | 0 | 9 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0002c0002t0006 | 0/0 | 9235 | 3 | 1 | 2 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0002c0002t0014 | 0/0 | 9235 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0002c0002t0022 | 0/0 | 9235 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0002c0011t0002 | 0/0 | 9235 | 2 | 0 | 2 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0002c0020t0002 | 0/0 | 9235 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0003c0003t0003 | 0/0 | 9235 | 12 | 11 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0003c0003t0023 | 0/0 | 9235 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0004c0004t0005 | 0/0 | 9235 | 4 | 0 | 0 | 3 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0004c0004t0012 | 0/0 | 9235 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0004c0004t0018 | 0/0 | 9234 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0004c0004t0019 | 0/0 | 9234 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0004c0004t0021 | 0/0 | 9235 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0005c0005t0003 | 0/0 | 9235 | 6 | 6 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0005c0005t0020 | 0/0 | 9235 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0006c0006t0002 | 0/0 | 9235 | 6 | 0 | 1 | 0 | 0 | 5 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0007c0008t0007 | 0/0 | 9235 | 4 | 4 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0008c0010t0008 | 0/0 | 9235 | 3 | 2 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0009c0009t0002 | 0/0 | 9235 | 3 | 3 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0010c0015t0003 | 0/0 | 9235 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0011c0014t0001 | 0/0 | 9232 | 2 | 0 | 0 | 2 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0012c0013t0011 | 0/0 | 9235 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0013c0012t0002 | 0/0 | 9235 | 2 | 0 | 0 | 0 | 0 | 2 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0014c0032t0002 | 0/0 | 9235 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0015c0030t0025 | 0/0 | 9234 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0016c0029t0016 | 0/0 | 9232 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0017c0028t0002 | 0/0 | 9235 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0018c0023t0005 | 0/0 | 9235 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0019c0031t0003 | 0/0 | 9235 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0020c0022t0002 | 0/0 | 9235 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0021c0025t0001 | 0/0 | 9232 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0022c0026t0015 | 0/0 | 9232 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0023c0027t0001 | 0/0 | 9232 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0024c0019t0002 | 0/0 | 9235 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0025c0018t0002 | 0/0 | 9235 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0026c0017t0002 | 0/0 | 9235 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0027c0021t0002 | 0/0 | 9235 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
a0028c0016t0006 | 0/0 | 9235 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | copy fasta | chr3 | 47845695 | 48021416 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0010g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0010g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0013g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0017g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0024g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0026g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0007t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0007t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0007t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0007t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0024t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0006g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0006g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0014g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0022g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0011t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0011t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0020t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0023g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0005g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0012g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0012g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0018g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0019g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0021g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0005c0005t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0005c0005t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0005c0005t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0005c0005t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0005c0005t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0005c0005t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0005c0005t0020g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0006c0006t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0006c0006t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0006c0006t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0006c0006t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0006c0006t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0006c0006t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0007c0008t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0007c0008t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0007c0008t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0007c0008t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0008c0010t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0008c0010t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0008c0010t0008g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0009c0009t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0009c0009t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0009c0009t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0010c0015t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0010c0015t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0011c0014t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0011c0014t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0012c0013t0011g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0012c0013t0011g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0013c0012t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0013c0012t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0014c0032t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0015c0030t0025g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0016c0029t0016g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0017c0028t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0018c0023t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0019c0031t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0020c0022t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0021c0025t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0022c0026t0015g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0023c0027t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0024c0019t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0025c0018t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0026c0017t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0027c0021t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0028c0016t0006g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | GBR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0025 | EUR | GBR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00280 | hp1 | a0001 | c0024 | t0001 | g0133 | EUR | FIN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0063 | EUR | FIN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00544 | hp1 | a0021 | c0025 | t0001 | g0215 | EAS | CHS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | CHS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00597 | hp2 | a0027 | c0021 | t0002 | g0011 | EAS | CHS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0123 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | CHS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00733 | hp1 | a0002 | c0011 | t0002 | g0073 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00735 | hp2 | a0023 | c0027 | t0001 | g0175 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00738 | hp1 | a0008 | c0010 | t0008 | g0113 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0231 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01074 | hp2 | a0002 | c0002 | t0006 | g0040 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0068 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01109 | hp2 | a0003 | c0003 | t0003 | g0095 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0061 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01255 | hp2 | a0002 | c0011 | t0002 | g0087 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01346 | hp1 | a0022 | c0026 | t0015 | g0148 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01346 | hp2 | a0028 | c0016 | t0006 | g0031 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01496 | hp1 | a0002 | c0002 | t0006 | g0028 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01496 | hp2 | a0025 | c0018 | t0002 | g0023 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01884 | hp1 | a0005 | c0005 | t0003 | g0117 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01891 | hp1 | a0007 | c0008 | t0007 | g0149 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01891 | hp2 | a0009 | c0009 | t0002 | g0047 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01934 | hp1 | a0004 | c0004 | t0021 | g0080 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0066 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02040 | hp1 | a0002 | c0002 | t0022 | g0064 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02040 | hp2 | a0004 | c0004 | t0005 | g0223 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02055 | hp2 | a0003 | c0003 | t0003 | g0107 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02071 | hp2 | a0018 | c0023 | t0005 | g0053 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02083 | hp2 | a0004 | c0004 | t0005 | g0084 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02145 | hp1 | a0002 | c0002 | t0002 | g0130 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02145 | hp2 | a0017 | c0028 | t0002 | g0224 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0024 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02258 | hp1 | a0009 | c0009 | t0002 | g0048 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02258 | hp2 | a0001 | c0001 | t0009 | g0167 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02273 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02280 | hp1 | a0001 | c0001 | t0010 | g0205 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02280 | hp2 | a0005 | c0005 | t0003 | g0115 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0051 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02451 | hp1 | a0001 | c0007 | t0001 | g0221 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02451 | hp2 | a0012 | c0013 | t0011 | g0002 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02572 | hp1 | a0001 | c0007 | t0001 | g0219 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02572 | hp2 | a0002 | c0002 | t0002 | g0056 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02602 | hp1 | a0006 | c0006 | t0002 | g0075 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02602 | hp2 | a0001 | c0001 | t0013 | g0204 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0069 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02630 | hp1 | a0003 | c0003 | t0003 | g0098 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02647 | hp1 | a0020 | c0022 | t0002 | g0088 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02647 | hp2 | a0001 | c0007 | t0001 | g0220 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02698 | hp2 | a0006 | c0006 | t0002 | g0062 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02717 | hp2 | a0010 | c0015 | t0003 | g0096 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02723 | hp1 | a0005 | c0005 | t0003 | g0121 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02723 | hp2 | a0002 | c0020 | t0002 | g0054 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0032 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02735 | hp2 | a0016 | c0029 | t0016 | g0155 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02738 | hp2 | a0006 | c0006 | t0002 | g0076 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02886 | hp1 | a0005 | c0005 | t0003 | g0119 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02886 | hp2 | a0010 | c0015 | t0003 | g0097 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02922 | hp1 | a0003 | c0003 | t0003 | g0110 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02922 | hp2 | a0012 | c0013 | t0011 | g0222 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02965 | hp2 | a0003 | c0003 | t0003 | g0104 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02970 | hp1 | a0007 | c0008 | t0007 | g0152 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02970 | hp2 | a0019 | c0031 | t0003 | g0109 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02976 | hp1 | a0003 | c0003 | t0003 | g0101 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02976 | hp2 | a0002 | c0002 | t0002 | g0125 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03041 | hp1 | a0003 | c0003 | t0003 | g0100 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03041 | hp2 | a0004 | c0004 | t0012 | g0049 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0055 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03098 | hp2 | a0009 | c0009 | t0002 | g0046 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03139 | hp2 | a0003 | c0003 | t0003 | g0102 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03225 | hp1 | a0005 | c0005 | t0003 | g0114 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03225 | hp2 | a0003 | c0003 | t0003 | g0099 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03453 | hp1 | a0004 | c0004 | t0012 | g0050 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03453 | hp2 | a0004 | c0004 | t0018 | g0083 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03486 | hp1 | a0003 | c0003 | t0003 | g0103 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03486 | hp2 | a0008 | c0010 | t0008 | g0112 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03491 | hp1 | a0004 | c0004 | t0005 | g0085 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03516 | hp1 | a0003 | c0003 | t0003 | g0108 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03516 | hp2 | a0001 | c0001 | t0026 | g0165 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0045 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03540 | hp2 | a0001 | c0007 | t0001 | g0218 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03579 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03579 | hp2 | a0003 | c0003 | t0003 | g0106 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03831 | hp2 | a0006 | c0006 | t0002 | g0074 | SAS | BEB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03834 | hp1 | a0006 | c0006 | t0002 | g0079 | SAS | BEB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03927 | hp2 | a0002 | c0002 | t0014 | g0065 | SAS | BEB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | STU | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG04115 | hp2 | a0013 | c0012 | t0002 | g0078 | SAS | STU | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG04204 | hp1 | a0024 | c0019 | t0002 | g0077 | SAS | STU | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | STU | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG04228 | hp2 | a0013 | c0012 | t0002 | g0071 | SAS | STU | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18522 | hp1 | a0014 | c0032 | t0002 | g0059 | AFR | YRI | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18522 | hp2 | a0001 | c0001 | t0017 | g0135 | AFR | YRI | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | CHB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18942 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18953 | hp1 | a0002 | c0002 | t0004 | g0019 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18956 | hp1 | a0002 | c0002 | t0004 | g0017 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18961 | hp1 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18969 | hp2 | a0026 | c0017 | t0002 | g0038 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18999 | hp2 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19000 | hp1 | a0004 | c0004 | t0005 | g0086 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19005 | hp2 | a0002 | c0002 | t0004 | g0015 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19006 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19006 | hp2 | a0001 | c0001 | t0024 | g0213 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19007 | hp1 | a0011 | c0014 | t0001 | g0143 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19007 | hp2 | a0002 | c0002 | t0004 | g0016 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19030 | hp1 | a0001 | c0001 | t0010 | g0178 | AFR | LWK | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19030 | hp2 | a0002 | c0002 | t0006 | g0026 | AFR | LWK | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19043 | hp2 | a0002 | c0002 | t0002 | g0082 | AFR | LWK | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19067 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19088 | hp1 | a0002 | c0002 | t0004 | g0009 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19091 | hp1 | a0011 | c0014 | t0001 | g0142 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19091 | hp2 | a0002 | c0002 | t0004 | g0006 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19240 | hp1 | a0007 | c0008 | t0007 | g0226 | AFR | YRI | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA20129 | hp1 | a0003 | c0003 | t0023 | g0105 | AFR | ASW | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA20129 | hp2 | a0008 | c0010 | t0008 | g0111 | AFR | ASW | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01123 | hp2 | a0006 | c0006 | t0002 | g0081 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02486 | hp1 | a0015 | c0030 | t0025 | g0044 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02486 | hp2 | a0004 | c0004 | t0019 | g0060 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02559 | hp1 | a0002 | c0002 | t0002 | g0057 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03471 | hp1 | a0001 | c0001 | t0009 | g0166 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03471 | hp2 | a0005 | c0005 | t0020 | g0116 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA20300 | hp1 | a0007 | c0008 | t0007 | g0131 | AFR | USA | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA20300 | hp2 | a0005 | c0005 | t0003 | g0122 | AFR | USA | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0070 | REF | REF | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0124 | REF | REF | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:47877426
|
C | A | 1 | a0019 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.5532G>T | p.Lys1844Asn | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/21 | 5634/9232 | 5532/6891 | 1844/2296 | chr3 | 47877426 | ||
chr3:47909184
|
G | C | 1 | a0009 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
missense_variant | MODERATE | c.5237C>G | p.Pro1746Arg | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 5339/9232 | 5237/6891 | 1746/2296 | chr3 | 47909184 | ||
chr3:47909809
|
T | C | 1 | a0026 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.4612A>G | p.Lys1538Glu | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 4714/9232 | 4612/6891 | 1538/2296 | chr3 | 47909809 | ||
chr3:47909913
|
G | A | 1 | a0025 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.4508C>T | p.Thr1503Ile | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 4610/9232 | 4508/6891 | 1503/2296 | chr3 | 47909913 | ||
chr3:47910180
|
A | G | 1 | a0009 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
missense_variant | MODERATE | c.4241T>C | p.Ile1414Thr | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 4343/9232 | 4241/6891 | 1414/2296 | chr3 | 47910180 | ||
chr3:47910484
|
T | C | 1 | a0024 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.3937A>G | p.Thr1313Ala | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 4039/9232 | 3937/6891 | 1313/2296 | chr3 | 47910484 | ||
chr3:47910660
|
G | A | 1 | a0008 | 3 | HG00738.hp1 HG03486.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.3761C>T | p.Pro1254Leu | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 3863/9232 | 3761/6891 | 1254/2296 | chr3 | 47910660 | ||
chr3:47910864
|
T | C | 1 | a0027 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.3557A>G | p.Asn1186Ser | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 3659/9232 | 3557/6891 | 1186/2296 | chr3 | 47910864 | ||
chr3:47911004
|
C | T | 1 | a0007 | 4 | HG01891.hp1 HG02970.hp1 NA19240.hp1 others(1): Show |
missense_variant | MODERATE | c.3417G>A | p.Met1139Ile | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 3519/9232 | 3417/6891 | 1139/2296 | chr3 | 47911004 | ||
chr3:47911145
|
C | G | 1 | a0011 | 2 | NA19007.hp1 NA19091.hp1 |
missense_variant | MODERATE | c.3276G>C | p.Lys1092Asn | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 3378/9232 | 3276/6891 | 1092/2296 | chr3 | 47911145 | ||
chr3:47911353
|
T | C | 1 | a0003 | 13 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(10): Show |
missense_variant | MODERATE | c.3068A>G | p.Asn1023Ser | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 3170/9232 | 3068/6891 | 1023/2296 | chr3 | 47911353 | ||
chr3:47911716
|
T | G | 1 | a0013 | 2 | HG04115.hp2 HG04228.hp2 |
missense_variant | MODERATE | c.2705A>C | p.Lys902Thr | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 2807/9232 | 2705/6891 | 902/2296 | chr3 | 47911716 | ||
chr3:47911750
|
G | C | 1 | a0018 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.2671C>G | p.Gln891Glu | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 2773/9232 | 2671/6891 | 891/2296 | chr3 | 47911750 | ||
chr3:47911915
|
A | C | 21 | a0002a0003a0004others(18): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
missense_variant | MODERATE | c.2506T>G | p.Leu836Val | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 2608/9232 | 2506/6891 | 836/2296 | chr3 | 47911915 | ||
chr3:47912067
|
G | A | 1 | a0021 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.2354C>T | p.Ala785Val | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 2456/9232 | 2354/6891 | 785/2296 | chr3 | 47912067 | ||
chr3:47912151
|
T | A | 1 | a0020 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.2270A>T | p.Glu757Val | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 2372/9232 | 2270/6891 | 757/2296 | chr3 | 47912151 | ||
chr3:47912243
|
C | A | 11 | a0002a0004a0006others(8): Show | 92 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(89): Show |
missense_variant | MODERATE | c.2178G>T | p.Trp726Cys | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 2280/9232 | 2178/6891 | 726/2296 | chr3 | 47912243 | ||
chr3:47912274
|
A | G | 1 | a0028 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.2147T>C | p.Leu716Pro | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 2249/9232 | 2147/6891 | 716/2296 | chr3 | 47912274 | ||
chr3:47912323
|
G | A | 1 | a0010 | 2 | HG02717.hp2 HG02886.hp2 |
missense_variant | MODERATE | c.2098C>T | p.Pro700Ser | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 2200/9232 | 2098/6891 | 700/2296 | chr3 | 47912323 | ||
chr3:47914894
|
T | C | 1 | a0022 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.1922A>G | p.Glu641Gly | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 8/21 | 2024/9232 | 1922/6891 | 641/2296 | chr3 | 47914894 | ||
chr3:47914934
|
C | T | 18 | a0002a0003a0004others(15): Show | 122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
missense_variant | MODERATE | c.1882G>A | p.Val628Ile | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 8/21 | 1984/9232 | 1882/6891 | 628/2296 | chr3 | 47914934 | ||
chr3:47915990
|
C | T | 1 | a0017 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.1837G>A | p.Val613Met | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/21 | 1939/9232 | 1837/6891 | 613/2296 | chr3 | 47915990 | ||
chr3:47916106
|
T | G | 1 | a0023 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.1721A>C | p.Lys574Thr | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/21 | 1823/9232 | 1721/6891 | 574/2296 | chr3 | 47916106 | ||
chr3:47916227
|
C | T | 1 | a0015 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1600G>A | p.Val534Ile | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/21 | 1702/9232 | 1600/6891 | 534/2296 | chr3 | 47916227 | ||
chr3:47916506
|
C | G | 1 | a0006 | 6 | HG01123.hp2 HG02602.hp1 HG02698.hp2 others(3): Show |
missense_variant | MODERATE | c.1321G>C | p.Glu441Gln | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/21 | 1423/9232 | 1321/6891 | 441/2296 | chr3 | 47916506 | ||
chr3:47916511
|
G | A | 1 | a0016 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.1316C>T | p.Ser439Phe | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/21 | 1418/9232 | 1316/6891 | 439/2296 | chr3 | 47916511 | ||
chr3:47916547
|
G | T | 9 | a0002a0006a0013others(6): Show | 82 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(79): Show |
missense_variant | MODERATE | c.1280C>A | p.Ser427Tyr | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/21 | 1382/9232 | 1280/6891 | 427/2296 | chr3 | 47916547 | ||
chr3:47917084
|
G | C | 1 | a0015 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.743C>G | p.Thr248Ser | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/21 | 845/9232 | 743/6891 | 248/2296 | chr3 | 47917084 | ||
chr3:47998684
|
G | C | 1 | a0014 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.177C>G | p.Asn59Lys | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/21 | 279/9232 | 177/6891 | 59/2296 | chr3 | 47998684 | ||
chr3:47998793
|
C | T | 1 | a0006 | 6 | HG01123.hp2 HG02602.hp1 HG02698.hp2 others(3): Show |
missense_variant | MODERATE | c.68G>A | p.Arg23Gln | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/21 | 170/9232 | 68/6891 | 23/2296 | chr3 | 47998793 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:47872008
|
C | T | 1 | a0002c0011 | 2 | HG00733.hp1 HG01255.hp2 |
synonymous_variant | LOW | c.5850G>A | p.Gln1950Gln | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 13/21 | 5952/9232 | 5850/6891 | 1950/2296 | chr3 | 47872008 | ||
chr3:47909144
|
T | C | 1 | a0020c0022 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.5277A>G | p.Glu1759Glu | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 5379/9232 | 5277/6891 | 1759/2296 | chr3 | 47909144 | ||
chr3:47910509
|
G | A | 1 | a0002c0020 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.3912C>T | p.Asn1304Asn | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 4014/9232 | 3912/6891 | 1304/2296 | chr3 | 47910509 | ||
chr3:47911019
|
C | T | 1 | a0001c0024 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.3402G>A | p.Thr1134Thr | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 3504/9232 | 3402/6891 | 1134/2296 | chr3 | 47911019 | ||
chr3:47916180
|
G | A | 1 | a0017c0028 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.1647C>T | p.Val549Val | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/21 | 1749/9232 | 1647/6891 | 549/2296 | chr3 | 47916180 | ||
chr3:47928244
|
G | A | 5 | a0003c0003a0005c0005a0008c0010others(2): Show | 26 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(23): Show |
synonymous_variant | LOW | c.399C>T | p.Val133Val | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/21 | 501/9232 | 399/6891 | 133/2296 | chr3 | 47928244 | ||
chr3:47998750
|
A | G | 1 | a0001c0007 | 4 | HG02451.hp1 HG02572.hp1 HG02647.hp2 others(1): Show |
synonymous_variant | LOW | c.111T>C | p.Val37Val | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/21 | 213/9232 | 111/6891 | 37/2296 | chr3 | 47998750 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:47850746
|
G | C | 1 | a0002c0002t0022 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2188C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 2188 | chr3 | 47850746 | |||||
chr3:47850886
|
C | CCTT | 35 | a0001c0001t0002a0001c0001t0010a0002c0002t0002others(32): Show | 129 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*2045_*2047dupAAG | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 2047 | chr3 | 47850886 | |||||
chr3:47850893
|
G | A | 7 | a0003c0003t0003a0003c0003t0023a0005c0005t0003others(4): Show | 26 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2041C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 2041 | chr3 | 47850893 | |||||
chr3:47850932
|
G | A | 1 | a0002c0002t0014 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2002C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 2002 | chr3 | 47850932 | |||||
chr3:47850941
|
G | T | 1 | a0022c0026t0015 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1993C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1993 | chr3 | 47850941 | |||||
chr3:47851024
|
A | AGAC | 1 | a0007c0008t0007 | 4 | HG01891.hp1 HG02970.hp1 NA19240.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1907_*1909dupGTC | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1909 | chr3 | 47851024 | |||||
chr3:47851084
|
A | T | 1 | a0001c0001t0009 | 2 | HG02258.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1850T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1850 | chr3 | 47851084 | |||||
chr3:47851089
|
G | C | 34 | a0001c0001t0002a0002c0002t0002a0002c0002t0004others(31): Show | 127 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*1845C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1845 | chr3 | 47851089 | |||||
chr3:47851293
|
G | A | 1 | a0004c0004t0018 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1641C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1641 | chr3 | 47851293 | |||||
chr3:47851365
|
C | T | 2 | a0002c0002t0006a0028c0016t0006 | 4 | HG01074.hp2 HG01346.hp2 HG01496.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1569G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1569 | chr3 | 47851365 | |||||
chr3:47851438
|
G | A | 1 | a0008c0010t0008 | 3 | HG00738.hp1 HG03486.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1496C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1496 | chr3 | 47851438 | |||||
chr3:47851453
|
T | C | 1 | a0015c0030t0025 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1481A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1481 | chr3 | 47851453 | |||||
chr3:47851764
|
T | G | 2 | a0004c0004t0019a0004c0004t0021 | 2 | HG01934.hp1 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1170A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1170 | chr3 | 47851764 | |||||
chr3:47852373
|
A | G | 1 | a0002c0002t0004 | 9 | NA18942.hp2 NA18953.hp1 NA18956.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*561T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 561 | chr3 | 47852373 | |||||
chr3:47852378
|
GA | G | 3 | a0004c0004t0018a0004c0004t0019a0015c0030t0025 | 3 | HG02486.hp1 HG02486.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*555delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 555 | chr3 | 47852378 | |||||
chr3:47852379
|
A | G | 5 | a0004c0004t0005a0004c0004t0012a0004c0004t0021others(2): Show | 9 | HG01934.hp1 HG02040.hp2 HG02071.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*555T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 555 | chr3 | 47852379 | |||||
chr3:47852380
|
G | C | 1 | a0004c0004t0012 | 2 | HG03041.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*554C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 554 | chr3 | 47852380 | |||||
chr3:47852381
|
G | A | 1 | a0003c0003t0023 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*553C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 553 | chr3 | 47852381 | |||||
chr3:47852442
|
T | A | 1 | a0001c0001t0024 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*492A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 492 | chr3 | 47852442 | |||||
chr3:47852451
|
C | T | 1 | a0001c0001t0017 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 483 | chr3 | 47852451 | |||||
chr3:47852556
|
T | G | 1 | a0015c0030t0025 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*378A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 378 | chr3 | 47852556 | |||||
chr3:47852611
|
C | T | 2 | a0016c0029t0016a0022c0026t0015 | 2 | HG01346.hp1 HG02735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*323G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 323 | chr3 | 47852611 | |||||
chr3:47852661
|
G | A | 2 | a0004c0004t0012a0012c0013t0011 | 4 | HG02451.hp2 HG02922.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*273C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 273 | chr3 | 47852661 | |||||
chr3:47852728
|
C | T | 2 | a0001c0001t0013a0002c0002t0014 | 2 | HG02602.hp2 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*206G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 206 | chr3 | 47852728 | |||||
chr3:47852877
|
T | A | 1 | a0001c0001t0026 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*57A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 57 | chr3 | 47852877 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:47852998
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.6887-60C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 20/20 | chr3 | 47852998 | ||||||
chr3:47853391
|
CGAG | C | 27 | a0002c0002t0002g0001a0002c0002t0002g0037a0002c0002t0002g0039others(24): Show | 28 | HG00280.hp2 HG00741.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.6697-42_6697-40del others(3): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853391 | ||||||
chr3:47853393
|
A | G | 6 | a0006c0006t0002g0062a0006c0006t0002g0074a0006c0006t0002g0075others(3): Show | 6 | HG01123.hp2 HG02602.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.6697-41T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853393 | ||||||
chr3:47853394
|
G | T | 35 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(32): Show | 35 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.6697-42C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853394 | ||||||
chr3:47853396
|
G | C | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6697-44C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853396 | ||||||
chr3:47853478
|
C | T | 1 | a0001c0001t0010g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6697-126G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853478 | ||||||
chr3:47853510
|
G | A | 1 | a0026c0017t0002g0038 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.6697-158C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853510 | ||||||
chr3:47853542
|
G | A | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6697-190C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853542 | ||||||
chr3:47853549
|
G | A | 2 | a0002c0002t0002g0092a0002c0002t0002g0093 | 2 | NA18970.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.6697-197C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853549 | ||||||
chr3:47853851
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6697-499C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853851 | ||||||
chr3:47853913
|
C | A | 16 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0012others(13): Show | 16 | HG00099.hp2 HG00673.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.6697-561G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853913 | ||||||
chr3:47854215
|
C | T | 2 | a0002c0002t0002g0069a0002c0002t0002g0231 | 2 | HG00741.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.6697-863G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854215 | ||||||
chr3:47854312
|
C | T | 2 | a0004c0004t0012g0049a0004c0004t0012g0050 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6696+936G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854312 | ||||||
chr3:47854324
|
C | T | 1 | a0004c0004t0005g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.6696+924G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854324 | ||||||
chr3:47854344
|
C | T | 16 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(13): Show | 16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.6696+904G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854344 | ||||||
chr3:47854465
|
C | T | 4 | a0005c0005t0003g0114a0005c0005t0003g0115a0005c0005t0003g0117others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.6696+783G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854465 | ||||||
chr3:47854559
|
A | G | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.6696+689T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854559 | ||||||
chr3:47854680
|
C | T | 1 | a0001c0007t0001g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.6696+568G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854680 | ||||||
chr3:47854720
|
A | AGCCCTGC others(19): Show |
2 | a0007c0008t0007g0149a0007c0008t0007g0152 | 2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6696+502_6696+527d others(28): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854720 | ||||||
chr3:47854720
|
AGCCCTGC others(19): Show |
A | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.6696+502_6696+527d others(28): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854720 | ||||||
chr3:47854808
|
G | A | 1 | a0002c0002t0002g0070 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.6696+440C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854808 | ||||||
chr3:47854899
|
C | G | 1 | a0002c0002t0004g0009 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.6696+349G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854899 | ||||||
chr3:47854935
|
C | G | 1 | a0001c0001t0001g0201 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.6696+313G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854935 | ||||||
chr3:47855036
|
A | G | 1 | a0002c0002t0002g0022 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.6696+212T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47855036 | ||||||
chr3:47855877
|
G | C | 1 | a0002c0002t0002g0231 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.6584-517C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 18/20 | chr3 | 47855877 | ||||||
chr3:47856379
|
A | G | 1 | a0004c0004t0012g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.6584-1019T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 18/20 | chr3 | 47856379 | ||||||
chr3:47856696
|
G | A | 1 | a0002c0002t0002g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.6583+735C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 18/20 | chr3 | 47856696 | ||||||
chr3:47856817
|
A | G | 94 | a0002c0002t0002g0001a0002c0002t0002g0027a0002c0002t0002g0029others(91): Show | 95 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.6583+614T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 18/20 | chr3 | 47856817 | ||||||
chr3:47856982
|
C | T | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.6583+449G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 18/20 | chr3 | 47856982 | ||||||
chr3:47857229
|
A | G | 31 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0010others(28): Show | 31 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.6583+202T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 18/20 | chr3 | 47857229 | ||||||
chr3:47857334
|
C | G | 1 | a0001c0001t0010g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6583+97G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 18/20 | chr3 | 47857334 | ||||||
chr3:47857568
|
AC | A | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-57delG | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857568 | ||||||
chr3:47857573
|
A | T | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-61T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857573 | ||||||
chr3:47857575
|
G | T | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-63C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857575 | ||||||
chr3:47857576
|
C | T | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-64G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857576 | ||||||
chr3:47857579
|
C | T | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-67G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857579 | ||||||
chr3:47857589
|
C | A | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-77G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857589 | ||||||
chr3:47857590
|
T | A | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-78A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857590 | ||||||
chr3:47857592
|
C | A | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-80G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857592 | ||||||
chr3:47857593
|
T | A | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-81A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857593 | ||||||
chr3:47857594
|
C | A | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-82G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857594 | ||||||
chr3:47857595
|
C | T | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-83G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857595 | ||||||
chr3:47857597
|
T | A | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-85A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857597 | ||||||
chr3:47857598
|
G | A | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-86C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857598 | ||||||
chr3:47857599
|
T | TAATAAAT others(67): Show |
7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-88_6502-87ins others(74): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857599 | ||||||
chr3:47858021
|
C | CT | 100 | a0001c0001t0001g0200a0001c0001t0001g0227a0002c0002t0002g0001others(97): Show | 101 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.6502-510dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858021 | ||||||
chr3:47858024
|
T | A | 1 | a0007c0008t0007g0226 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6502-512A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858024 | ||||||
chr3:47858076
|
C | T | 1 | a0002c0002t0002g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.6502-564G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858076 | ||||||
chr3:47858388
|
G | T | 33 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0134others(30): Show | 33 | HG00544.hp1 HG00609.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.6502-876C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858388 | ||||||
chr3:47858586
|
G | GGT | 9 | a0001c0001t0001g0128a0001c0001t0001g0214a0001c0001t0001g0216others(6): Show | 9 | HG00544.hp1 NA18940.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.6502-1076_6502-107 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858586 | ||||||
chr3:47858586
|
G | GGTGT | 37 | a0002c0002t0002g0001a0002c0002t0002g0052a0002c0002t0002g0055others(34): Show | 38 | HG00280.hp2 HG00639.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.6502-1078_6502-107 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858586 | ||||||
chr3:47858586
|
G | GGTGTGT | 13 | a0002c0002t0002g0082a0002c0002t0002g0093a0002c0002t0014g0065others(10): Show | 13 | HG00733.hp1 HG00738.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.6502-1080_6502-107 others(10): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858586 | ||||||
chr3:47858586
|
G | GGTGTGTG others(1): Show |
5 | a0003c0003t0003g0098a0003c0003t0003g0099a0005c0005t0003g0119others(2): Show | 5 | HG02630.hp1 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.6502-1082_6502-107 others(12): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858586 | ||||||
chr3:47858586
|
G | GGTGTGTG others(3): Show |
15 | a0002c0002t0002g0070a0003c0003t0003g0095a0003c0003t0003g0100others(12): Show | 15 | HG01109.hp2 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.6502-1084_6502-107 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858586 | ||||||
chr3:47858586
|
G | GGTGTGTG others(5): Show |
5 | a0004c0004t0012g0049a0004c0004t0012g0050a0010c0015t0003g0096others(2): Show | 5 | HG02717.hp2 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.6502-1086_6502-107 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858586 | ||||||
chr3:47858586
|
G | GGTGTGTG others(7): Show |
1 | a0009c0009t0002g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6502-1088_6502-107 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858586 | ||||||
chr3:47858586
|
GGT | G | 4 | a0001c0001t0001g0132a0001c0001t0001g0190a0001c0001t0001g0227others(1): Show | 4 | HG02083.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.6502-1076_6502-107 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858586 | ||||||
chr3:47858614
|
T | C | 5 | a0004c0004t0005g0084a0007c0008t0007g0149a0007c0008t0007g0152others(2): Show | 5 | HG01891.hp1 HG02083.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.6502-1102A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858614 | ||||||
chr3:47858614
|
T | TGTGC | 4 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0032others(1): Show | 4 | HG00544.hp2 HG02735.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.6502-1103_6502-110 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858614 | ||||||
chr3:47858616
|
C | T | 11 | a0001c0001t0001g0141a0002c0002t0002g0045a0002c0002t0002g0056others(8): Show | 11 | HG01255.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.6502-1104G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858616 | ||||||
chr3:47858620
|
T | C | 22 | a0002c0002t0002g0030a0002c0002t0002g0034a0002c0002t0002g0035others(19): Show | 22 | HG01884.hp1 HG02040.hp2 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.6502-1108A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858620 | ||||||
chr3:47858620
|
T | TTG | 6 | a0001c0001t0001g0196a0001c0001t0001g0197a0009c0009t0002g0046others(3): Show | 6 | HG00735.hp2 HG01109.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.6502-1110_6502-110 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858620 | ||||||
chr3:47858620
|
TTG | T | 93 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(90): Show | 94 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.6502-1110_6502-110 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858620 | ||||||
chr3:47858621
|
T | G | 23 | a0002c0002t0002g0030a0002c0002t0002g0034a0002c0002t0002g0035others(20): Show | 23 | HG01884.hp1 HG02040.hp2 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.6502-1109A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858621 | ||||||
chr3:47858622
|
G | T | 23 | a0002c0002t0002g0030a0002c0002t0002g0034a0002c0002t0002g0035others(20): Show | 23 | HG01884.hp1 HG02040.hp2 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.6502-1110C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858622 | ||||||
chr3:47858895
|
A | G | 1 | a0002c0002t0002g0063 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.6502-1383T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858895 | ||||||
chr3:47859213
|
C | T | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.6502-1701G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47859213 | ||||||
chr3:47859444
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0136a0001c0001t0017g0135 | 3 | HG03139.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6502-1932C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47859444 | ||||||
chr3:47859649
|
A | G | 1 | a0004c0004t0012g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.6502-2137T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47859649 | ||||||
chr3:47859897
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.6502-2385G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47859897 | ||||||
chr3:47859989
|
A | C | 1 | a0004c0004t0005g0085 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.6502-2477T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47859989 | ||||||
chr3:47860255
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.6502-2743C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47860255 | ||||||
chr3:47860313
|
C | A | 90 | a0002c0002t0002g0001a0002c0002t0002g0027a0002c0002t0002g0029others(87): Show | 91 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.6502-2801G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47860313 | ||||||
chr3:47860757
|
C | T | 8 | a0002c0002t0002g0045a0002c0002t0002g0055a0002c0002t0002g0056others(5): Show | 8 | HG02559.hp1 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.6502-3245G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47860757 | ||||||
chr3:47860994
|
C | T | 1 | a0017c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6502-3482G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47860994 | ||||||
chr3:47861153
|
G | T | 1 | a0001c0001t0001g0134 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.6502-3641C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47861153 | ||||||
chr3:47861353
|
C | CT | 86 | a0001c0001t0001g0144a0001c0001t0001g0158a0001c0001t0001g0189others(83): Show | 87 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.6502-3842dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47861353 | ||||||
chr3:47861353
|
C | CTT | 9 | a0003c0003t0003g0107a0004c0004t0005g0086a0004c0004t0021g0080others(6): Show | 9 | HG01123.hp2 HG01884.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.6502-3843_6502-384 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47861353 | ||||||
chr3:47861470
|
A | T | 1 | a0004c0004t0019g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6502-3958T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47861470 | ||||||
chr3:47861693
|
G | C | 2 | a0001c0001t0001g0128a0009c0009t0002g0047 | 2 | HG01891.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.6502-4181C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47861693 | ||||||
chr3:47861764
|
C | A | 1 | a0002c0002t0002g0036 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.6502-4252G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47861764 | ||||||
chr3:47861815
|
C | T | 50 | a0002c0002t0002g0001a0002c0002t0002g0027a0002c0002t0002g0029others(47): Show | 51 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.6502-4303G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47861815 | ||||||
chr3:47861934
|
G | A | 50 | a0002c0002t0002g0001a0002c0002t0002g0027a0002c0002t0002g0029others(47): Show | 51 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.6502-4422C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47861934 | ||||||
chr3:47862029
|
C | T | 1 | a0004c0004t0018g0083 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6502-4517G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862029 | ||||||
chr3:47862161
|
C | CA | 15 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0141others(12): Show | 15 | HG00609.hp1 HG01109.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.6502-4650dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862161 | ||||||
chr3:47862161
|
CA | C | 35 | a0001c0001t0001g0211a0002c0002t0002g0004a0002c0002t0002g0010others(32): Show | 35 | HG00099.hp2 HG00673.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.6502-4650delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862161 | ||||||
chr3:47862161
|
CAA | C | 81 | a0002c0002t0002g0001a0002c0002t0002g0027a0002c0002t0002g0029others(78): Show | 82 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.6502-4651_6502-465 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862161 | ||||||
chr3:47862346
|
C | CA | 23 | a0001c0001t0001g0147a0001c0001t0001g0163a0001c0001t0001g0170others(20): Show | 23 | HG00544.hp1 HG00609.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.6502-4835dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | ||||||
chr3:47862346
|
C | CAA | 5 | a0001c0001t0001g0156a0001c0001t0001g0173a0001c0001t0001g0177others(2): Show | 5 | HG01891.hp1 HG02071.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.6502-4836_6502-483 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | ||||||
chr3:47862346
|
CA | C | 31 | a0001c0001t0001g0043a0001c0001t0001g0137a0001c0001t0001g0139others(28): Show | 32 | HG00280.hp1 HG00280.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.6502-4835delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | ||||||
chr3:47862346
|
CAA | C | 12 | a0002c0002t0002g0090a0003c0003t0003g0102a0004c0004t0005g0084others(9): Show | 12 | HG01934.hp1 HG02040.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.6502-4836_6502-483 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | ||||||
chr3:47862346
|
CAAA | C | 27 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(24): Show | 27 | HG00544.hp2 HG00738.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.6502-4837_6502-483 others(7): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | ||||||
chr3:47862346
|
CAAAA | C | 9 | a0005c0005t0003g0114a0005c0005t0003g0115a0005c0005t0003g0117others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.6502-4838_6502-483 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | ||||||
chr3:47862346
|
CAAAAAAA | C | 14 | a0002c0002t0002g0045a0002c0002t0002g0055a0002c0002t0002g0056others(11): Show | 14 | HG01123.hp2 HG02451.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.6502-4841_6502-483 others(11): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | ||||||
chr3:47862346
|
CAAAAAAA others(2): Show |
C | 10 | a0002c0002t0002g0020a0002c0002t0002g0036a0002c0002t0002g0037others(7): Show | 10 | HG01074.hp2 HG01346.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.6502-4843_6502-483 others(13): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | ||||||
chr3:47862346
|
CAAAAAAA others(3): Show |
C | 24 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0010others(21): Show | 24 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.6502-4844_6502-483 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | ||||||
chr3:47862445
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.6501+4801A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862445 | ||||||
chr3:47863063
|
G | A | 4 | a0002c0002t0002g0021a0002c0002t0002g0024a0002c0002t0002g0025others(1): Show | 4 | HG00099.hp2 HG01496.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.6501+4183C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863063 | ||||||
chr3:47863454
|
C | T | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.6501+3792G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863454 | ||||||
chr3:47863589
|
G | A | 50 | a0002c0002t0002g0001a0002c0002t0002g0027a0002c0002t0002g0029others(47): Show | 51 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.6501+3657C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863589 | ||||||
chr3:47863674
|
T | A | 1 | a0004c0004t0019g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6501+3572A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863674 | ||||||
chr3:47863921
|
G | GGGGTGTG others(7): Show |
1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6501+3324_6501+332 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863921 | ||||||
chr3:47863921
|
G | GGTGTGTG others(7): Show |
31 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0010others(28): Show | 31 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.6501+3311_6501+332 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863921 | ||||||
chr3:47863921
|
G | GGTGTGTG others(9): Show |
1 | a0002c0002t0002g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6501+3309_6501+332 others(20): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863921 | ||||||
chr3:47863921
|
G | GGTGTGTG others(13): Show |
1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6501+3324_6501+332 others(24): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863921 | ||||||
chr3:47863921
|
G | GGTGTGTG others(31): Show |
1 | a0017c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6501+3324_6501+332 others(42): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863921 | ||||||
chr3:47863921
|
G | T | 1 | a0004c0004t0005g0084 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6501+3325C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863921 | ||||||
chr3:47863923
|
T | G | 1 | a0001c0001t0001g0208 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.6501+3323A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863923 | ||||||
chr3:47863937
|
T | TGTGGGGG others(6): Show |
2 | a0002c0002t0002g0052a0002c0002t0002g0072 | 2 | HG02015.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(17): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | ||||||
chr3:47863937
|
T | TGTGTGGG others(3): Show |
1 | a0009c0009t0002g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6501+3308_6501+330 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | ||||||
chr3:47863937
|
T | TGTGTGGG others(4): Show |
1 | a0014c0032t0002g0059 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6501+3308_6501+330 others(15): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | ||||||
chr3:47863937
|
T | TGTGTGGG others(5): Show |
11 | a0002c0002t0002g0027a0002c0002t0002g0032a0002c0002t0002g0033others(8): Show | 11 | HG02559.hp1 HG02735.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | ||||||
chr3:47863937
|
T | TGTGTGGG others(6): Show |
2 | a0002c0002t0002g0029a0002c0002t0002g0030 | 2 | HG00544.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(17): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | ||||||
chr3:47863937
|
T | TGTGTGGG others(7): Show |
1 | a0024c0019t0002g0077 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6501+3308_6501+330 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | ||||||
chr3:47863937
|
T | TGTGTGTG others(3): Show |
3 | a0003c0003t0003g0102a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | ||||||
chr3:47863937
|
T | TGTGTGTG others(5): Show |
29 | a0002c0002t0002g0001a0002c0002t0002g0045a0002c0002t0002g0051others(26): Show | 30 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | ||||||
chr3:47863937
|
T | TGTGTGTG others(6): Show |
2 | a0002c0002t0002g0066a0002c0002t0002g0068 | 2 | HG01099.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(17): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | ||||||
chr3:47863937
|
T | TGTGTGTG others(7): Show |
1 | a0004c0004t0021g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.6501+3308_6501+330 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | ||||||
chr3:47863937
|
T | TGTGTGTG others(35): Show |
1 | a0012c0013t0011g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6501+3308_6501+330 others(46): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | ||||||
chr3:47863937
|
T | TGTGTGTG others(3): Show |
24 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(21): Show | 24 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | ||||||
chr3:47863937
|
T | TGTGTGTG others(5): Show |
2 | a0002c0002t0002g0231a0004c0004t0018g0083 | 2 | HG00741.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | ||||||
chr3:47863937
|
T | TGTGTGTG others(7): Show |
1 | a0004c0004t0012g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6501+3308_6501+330 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | ||||||
chr3:47863937
|
T | TGTGTGTG others(5): Show |
1 | a0003c0003t0003g0103 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.6501+3308_6501+330 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | ||||||
chr3:47863937
|
T | TGTGTGTG others(7): Show |
7 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(4): Show | 7 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | ||||||
chr3:47864046
|
C | T | 10 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(7): Show | 10 | HG01934.hp1 HG02040.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.6501+3200G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864046 | ||||||
chr3:47864080
|
G | C | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.6501+3166C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864080 | ||||||
chr3:47864414
|
T | C | 4 | a0002c0002t0002g0123a0002c0011t0002g0073a0002c0011t0002g0087others(1): Show | 4 | HG00639.hp1 HG00733.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.6501+2832A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864414 | ||||||
chr3:47864451
|
C | T | 1 | a0002c0002t0006g0028 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.6501+2795G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864451 | ||||||
chr3:47864521
|
T | TA | 3 | a0001c0007t0001g0218a0007c0008t0007g0131a0007c0008t0007g0226 | 3 | HG03540.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6501+2724dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864521 | ||||||
chr3:47864577
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.6501+2669A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864577 | ||||||
chr3:47864614
|
T | C | 6 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 6 | HG01255.hp1 HG02015.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.6501+2632A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864614 | ||||||
chr3:47864620
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.6501+2626A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864620 | ||||||
chr3:47864693
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.6501+2553G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864693 | ||||||
chr3:47864781
|
C | T | 1 | a0002c0002t0002g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6501+2465G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864781 | ||||||
chr3:47864818
|
G | A | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6501+2428C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864818 | ||||||
chr3:47864845
|
C | T | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6501+2401G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864845 | ||||||
chr3:47865135
|
CAAAA | C | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.6501+2107_6501+211 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47865135 | ||||||
chr3:47865516
|
G | GGA | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.6501+1728_6501+172 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47865516 | ||||||
chr3:47865856
|
G | A | 4 | a0001c0001t0001g0126a0001c0001t0001g0200a0001c0001t0001g0201others(1): Show | 4 | HG00609.hp1 HG00673.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.6501+1390C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47865856 | ||||||
chr3:47866168
|
C | T | 1 | a0002c0002t0002g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.6501+1078G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47866168 | ||||||
chr3:47866229
|
T | C | 126 | a0001c0001t0001g0183a0002c0002t0002g0001a0002c0002t0002g0004others(123): Show | 127 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.6501+1017A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47866229 | ||||||
chr3:47866347
|
A | AAAAC | 4 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(1): Show | 4 | HG02922.hp2 NA18946.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.6501+895_6501+898d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47866347 | ||||||
chr3:47866347
|
AAAAC | A | 4 | a0001c0001t0010g0178a0002c0002t0014g0065a0004c0004t0012g0049others(1): Show | 4 | HG03041.hp2 HG03453.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.6501+895_6501+898d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47866347 | ||||||
chr3:47866359
|
C | G | 1 | a0003c0003t0003g0099 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6501+887G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47866359 | ||||||
chr3:47866474
|
G | A | 1 | a0001c0001t0010g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6501+772C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47866474 | ||||||
chr3:47866639
|
G | A | 17 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(14): Show | 17 | HG01109.hp2 HG02055.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.6501+607C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47866639 | ||||||
chr3:47867192
|
A | G | 1 | a0002c0002t0002g0036 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.6501+54T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47867192 | ||||||
chr3:47867571
|
C | T | 1 | a0002c0002t0004g0015 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.6409-233G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 16/20 | chr3 | 47867571 | ||||||
chr3:47867591
|
C | T | 1 | a0004c0004t0019g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6409-253G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 16/20 | chr3 | 47867591 | ||||||
chr3:47867703
|
C | G | 2 | a0004c0004t0012g0049a0004c0004t0012g0050 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6409-365G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 16/20 | chr3 | 47867703 | ||||||
chr3:47867890
|
G | C | 5 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(2): Show | 5 | HG01074.hp1 HG01169.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.6409-552C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 16/20 | chr3 | 47867890 | ||||||
chr3:47868365
|
A | T | 1 | a0002c0002t0002g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.6408+849T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 16/20 | chr3 | 47868365 | ||||||
chr3:47868547
|
C | T | 1 | a0023c0027t0001g0175 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.6408+667G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 16/20 | chr3 | 47868547 | ||||||
chr3:47868598
|
C | T | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6408+616G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 16/20 | chr3 | 47868598 | ||||||
chr3:47869540
|
A | C | 1 | a0002c0002t0002g0120 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.6295-213T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47869540 | ||||||
chr3:47869631
|
G | A | 3 | a0002c0002t0002g0001a0002c0002t0002g0061a0002c0002t0002g0068 | 4 | HG01099.hp1 HG01169.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.6295-304C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47869631 | ||||||
chr3:47869701
|
A | G | 1 | a0012c0013t0011g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6295-374T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47869701 | ||||||
chr3:47869701
|
A | T | 1 | a0002c0002t0002g0120 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.6295-374T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47869701 | ||||||
chr3:47869784
|
A | C | 1 | a0005c0005t0003g0117 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6295-457T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47869784 | ||||||
chr3:47869830
|
C | G | 4 | a0002c0002t0006g0026a0002c0002t0006g0028a0002c0002t0006g0040others(1): Show | 4 | HG01074.hp2 HG01346.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.6295-503G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47869830 | ||||||
chr3:47870031
|
C | T | 38 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0010others(35): Show | 38 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.6295-704G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47870031 | ||||||
chr3:47870157
|
C | G | 1 | a0001c0001t0001g0187 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.6294+656G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47870157 | ||||||
chr3:47870237
|
C | T | 31 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0010others(28): Show | 31 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.6294+576G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47870237 | ||||||
chr3:47870268
|
T | C | 2 | a0007c0008t0007g0131a0007c0008t0007g0226 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6294+545A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47870268 | ||||||
chr3:47871536
|
A | AGCCCTCT others(31): Show |
1 | a0002c0002t0002g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5942-288_5942-251d others(40): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 13/20 | chr3 | 47871536 | ||||||
chr3:47872636
|
C | A | 1 | a0007c0008t0007g0226 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5758-536G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47872636 | ||||||
chr3:47872796
|
C | G | 1 | a0017c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5758-696G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47872796 | ||||||
chr3:47872972
|
T | G | 1 | a0005c0005t0020g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5758-872A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47872972 | ||||||
chr3:47872986
|
G | A | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.5758-886C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47872986 | ||||||
chr3:47873287
|
G | A | 4 | a0002c0002t0006g0026a0002c0002t0006g0028a0002c0002t0006g0040others(1): Show | 4 | HG01074.hp2 HG01346.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.5758-1187C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47873287 | ||||||
chr3:47873339
|
G | A | 29 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(26): Show | 29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.5758-1239C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47873339 | ||||||
chr3:47873484
|
C | T | 4 | a0001c0001t0001g0208a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.5758-1384G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47873484 | ||||||
chr3:47873541
|
T | G | 3 | a0008c0010t0008g0111a0008c0010t0008g0112a0008c0010t0008g0113 | 3 | HG00738.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.5758-1441A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47873541 | ||||||
chr3:47873592
|
A | T | 2 | a0002c0002t0002g0045a0002c0002t0002g0055 | 2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5758-1492T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47873592 | ||||||
chr3:47873628
|
A | G | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.5758-1528T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47873628 | ||||||
chr3:47874215
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.5757+1470G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47874215 | ||||||
chr3:47874293
|
C | T | 1 | a0002c0002t0002g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5757+1392G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47874293 | ||||||
chr3:47874450
|
C | G | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5757+1235G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47874450 | ||||||
chr3:47874909
|
A | G | 1 | a0002c0002t0002g0033 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.5757+776T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47874909 | ||||||
chr3:47875002
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5757+683A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47875002 | ||||||
chr3:47875658
|
C | T | 1 | a0002c0002t0002g0039 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5757+27G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47875658 | ||||||
chr3:47876132
|
C | CT | 3 | a0001c0001t0001g0211a0001c0001t0001g0229a0001c0007t0001g0219 | 3 | HG01257.hp2 HG02572.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5542-233dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/20 | chr3 | 47876132 | ||||||
chr3:47876132
|
CTTTCTT | C | 120 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(117): Show | 121 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.5542-238_5542-233d others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/20 | chr3 | 47876132 | ||||||
chr3:47876136
|
C | T | 51 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(48): Show | 51 | HG00544.hp1 HG00609.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.5542-236G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/20 | chr3 | 47876136 | ||||||
chr3:47876244
|
G | C | 1 | a0001c0001t0001g0161 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5542-344C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/20 | chr3 | 47876244 | ||||||
chr3:47876282
|
C | A | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5542-382G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/20 | chr3 | 47876282 | ||||||
chr3:47876557
|
CAGG | C | 29 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(26): Show | 29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.5542-660_5542-658d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/20 | chr3 | 47876557 | ||||||
chr3:47876885
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5541+532C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/20 | chr3 | 47876885 | ||||||
chr3:47876903
|
C | CT | 9 | a0001c0001t0001g0126a0001c0001t0001g0134a0001c0001t0001g0200others(6): Show | 9 | HG00609.hp1 HG00639.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.5541+513dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/20 | chr3 | 47876903 | ||||||
chr3:47877793
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.5435-270A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47877793 | ||||||
chr3:47877846
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.5435-323A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47877846 | ||||||
chr3:47878139
|
T | C | 1 | a0002c0002t0002g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5435-616A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47878139 | ||||||
chr3:47878227
|
G | A | 3 | a0002c0002t0006g0028a0002c0002t0006g0040a0028c0016t0006g0031 | 3 | HG01074.hp2 HG01346.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.5435-704C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47878227 | ||||||
chr3:47878750
|
C | T | 81 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(78): Show | 82 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.5435-1227G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47878750 | ||||||
chr3:47878847
|
A | ATT | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.5435-1326_5435-132 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47878847 | ||||||
chr3:47879240
|
GA | G | 15 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(12): Show | 15 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.5435-1718delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47879240 | ||||||
chr3:47879318
|
T | C | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5435-1795A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47879318 | ||||||
chr3:47879675
|
AACC | A | 80 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(77): Show | 81 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.5435-2155_5435-215 others(7): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47879675 | ||||||
chr3:47879752
|
T | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0216 | 2 | NA18982.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.5435-2229A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47879752 | ||||||
chr3:47879903
|
G | A | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5435-2380C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47879903 | ||||||
chr3:47880021
|
TGA | T | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5435-2500_5435-249 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880021 | ||||||
chr3:47880061
|
G | A | 1 | a0002c0002t0002g0089 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.5435-2538C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880061 | ||||||
chr3:47880180
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.5435-2657G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880180 | ||||||
chr3:47880214
|
C | T | 38 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0010others(35): Show | 38 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.5435-2691G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880214 | ||||||
chr3:47880251
|
C | G | 1 | a0001c0001t0001g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5435-2728G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880251 | ||||||
chr3:47880259
|
A | AT | 17 | a0001c0001t0001g0129a0001c0001t0001g0139a0001c0001t0001g0153others(14): Show | 17 | HG00741.hp1 HG01981.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.5435-2737dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880259 | ||||||
chr3:47880259
|
AT | A | 77 | a0001c0001t0001g0147a0001c0001t0001g0156a0001c0001t0001g0159others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.5435-2737delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880259 | ||||||
chr3:47880259
|
ATT | A | 6 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(3): Show | 6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.5435-2738_5435-273 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880259 | ||||||
chr3:47880302
|
G | A | 2 | a0002c0002t0002g0069a0002c0002t0002g0231 | 2 | HG00741.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.5435-2779C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880302 | ||||||
chr3:47880343
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.5435-2820G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880343 | ||||||
chr3:47880359
|
C | T | 1 | a0004c0004t0018g0083 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5435-2836G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880359 | ||||||
chr3:47880393
|
C | A | 2 | a0013c0012t0002g0071a0013c0012t0002g0078 | 2 | HG04115.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.5435-2870G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880393 | ||||||
chr3:47880465
|
G | GT | 15 | a0001c0001t0001g0151a0001c0001t0001g0157a0001c0001t0001g0160others(12): Show | 15 | HG00544.hp1 HG00741.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.5435-2943dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880465 | ||||||
chr3:47880465
|
G | GTT | 91 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0010others(88): Show | 92 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.5435-2944_5435-294 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880465 | ||||||
chr3:47880465
|
G | GTTT | 16 | a0002c0002t0002g0004a0002c0002t0002g0012a0002c0002t0002g0024others(13): Show | 16 | HG00597.hp2 HG00735.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.5435-2945_5435-294 others(7): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880465 | ||||||
chr3:47880465
|
GT | G | 5 | a0001c0001t0001g0146a0001c0001t0001g0171a0001c0001t0001g0187others(2): Show | 5 | HG01099.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.5435-2943delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880465 | ||||||
chr3:47880508
|
T | C | 2 | a0001c0001t0009g0166a0001c0001t0009g0167 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5435-2985A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880508 | ||||||
chr3:47880673
|
A | C | 1 | a0002c0002t0002g0018 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.5435-3150T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880673 | ||||||
chr3:47880690
|
C | T | 2 | a0002c0002t0002g0037a0002c0002t0002g0039 | 2 | HG02135.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.5435-3167G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880690 | ||||||
chr3:47880753
|
A | ATGCCCCA others(17): Show |
1 | a0002c0002t0002g0120 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.5435-3254_5435-323 others(28): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880753 | ||||||
chr3:47881446
|
C | CTA | 12 | a0001c0001t0001g0137a0001c0001t0001g0144a0001c0001t0001g0158others(9): Show | 12 | HG01109.hp1 HG01516.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.5435-3925_5435-392 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
C | CTACATAT others(5): Show |
1 | a0001c0001t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.5435-3924_5435-392 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
C | CTATA | 19 | a0001c0001t0001g0067a0001c0001t0001g0126a0001c0001t0001g0141others(16): Show | 19 | HG00544.hp1 HG00609.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.5435-3927_5435-392 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
C | CTATATA | 18 | a0001c0001t0001g0128a0001c0001t0001g0132a0001c0001t0001g0136others(15): Show | 18 | HG00735.hp2 HG01123.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.5435-3929_5435-392 others(10): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
C | CTATATAT others(1): Show |
13 | a0001c0001t0001g0139a0001c0001t0001g0160a0001c0001t0001g0171others(10): Show | 13 | HG00609.hp2 HG00741.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.5435-3931_5435-392 others(12): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
C | CTATATAT others(3): Show |
9 | a0001c0001t0001g0042a0001c0001t0001g0140a0001c0001t0001g0164others(6): Show | 9 | HG01943.hp2 HG02148.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.5435-3933_5435-392 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
C | CTATATAT others(5): Show |
5 | a0001c0001t0001g0134a0003c0003t0003g0099a0008c0010t0008g0113others(2): Show | 5 | HG00639.hp2 HG00738.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.5435-3935_5435-392 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
C | CTATATAT others(7): Show |
2 | a0001c0001t0001g0199a0001c0001t0001g0225 | 2 | HG01884.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.5435-3937_5435-392 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
C | CTATATAT others(9): Show |
1 | a0001c0001t0001g0189 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.5435-3939_5435-392 others(20): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
C | CTATATAT others(17): Show |
2 | a0001c0001t0001g0157a0001c0001t0026g0165 | 2 | HG03516.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.5435-3947_5435-392 others(28): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
CTA | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0196a0001c0001t0001g0210others(3): Show | 6 | HG01934.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.5435-3925_5435-392 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
CTATA | C | 12 | a0001c0001t0001g0146a0001c0001t0001g0161a0001c0001t0001g0169others(9): Show | 12 | HG00099.hp1 HG01099.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.5435-3927_5435-392 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
CTATATA | C | 4 | a0001c0001t0001g0195a0001c0001t0001g0209a0003c0003t0003g0100others(1): Show | 4 | HG00738.hp2 HG03041.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.5435-3929_5435-392 others(10): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
CTATATAT others(1): Show |
C | 5 | a0001c0001t0001g0229a0001c0007t0001g0218a0001c0007t0001g0219others(2): Show | 5 | HG02572.hp1 HG02735.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.5435-3931_5435-392 others(12): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
CTATATAT others(3): Show |
C | 7 | a0001c0001t0001g0187a0001c0001t0001g0192a0001c0001t0001g0206others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.5435-3933_5435-392 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
CTATATAT others(5): Show |
C | 3 | a0001c0001t0001g0041a0001c0001t0010g0205a0005c0005t0003g0121 | 3 | HG02280.hp1 HG02723.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.5435-3935_5435-392 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
CTATATAT others(7): Show |
C | 1 | a0002c0002t0002g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5435-3937_5435-392 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
CTATATAT others(9): Show |
C | 13 | a0001c0001t0001g0151a0001c0001t0001g0159a0002c0002t0002g0045others(10): Show | 13 | HG01891.hp2 HG02572.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.5435-3939_5435-392 others(20): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
CTATATAT others(11): Show |
C | 19 | a0001c0024t0001g0133a0002c0002t0002g0051a0002c0002t0002g0052others(16): Show | 19 | HG00280.hp1 HG01981.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.5435-3941_5435-392 others(22): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
CTATATAT others(13): Show |
C | 17 | a0001c0001t0001g0043a0002c0002t0002g0063a0002c0002t0002g0068others(14): Show | 17 | HG00280.hp2 HG00639.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.5435-3943_5435-392 others(24): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
CTATATAT others(15): Show |
C | 15 | a0002c0002t0002g0001a0002c0002t0002g0061a0002c0002t0002g0069others(12): Show | 16 | HG00733.hp1 HG00741.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.5435-3945_5435-392 others(26): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
CTATATAT others(17): Show |
C | 37 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0010others(34): Show | 37 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.5435-3947_5435-392 others(28): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881446
|
CTATATAT others(19): Show |
C | 1 | a0012c0013t0011g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5435-3949_5435-392 others(30): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | ||||||
chr3:47881488
|
A | G | 1 | a0001c0001t0002g0150 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.5435-3965T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881488 | ||||||
chr3:47881489
|
T | C | 1 | a0001c0001t0002g0150 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.5435-3966A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881489 | ||||||
chr3:47881807
|
G | T | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.5435-4284C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881807 | ||||||
chr3:47881931
|
T | C | 6 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(3): Show | 6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.5435-4408A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881931 | ||||||
chr3:47882044
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5435-4521G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47882044 | ||||||
chr3:47882136
|
G | C | 1 | a0023c0027t0001g0175 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.5435-4613C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47882136 | ||||||
chr3:47882143
|
G | A | 4 | a0001c0007t0001g0218a0001c0007t0001g0219a0001c0007t0001g0220others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.5435-4620C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47882143 | ||||||
chr3:47882509
|
T | TA | 29 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(26): Show | 29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.5435-4987dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47882509 | ||||||
chr3:47882726
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5435-5203G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47882726 | ||||||
chr3:47882757
|
G | C | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5435-5234C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47882757 | ||||||
chr3:47882827
|
G | C | 120 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(117): Show | 121 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.5435-5304C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47882827 | ||||||
chr3:47882895
|
C | T | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5435-5372G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47882895 | ||||||
chr3:47883926
|
G | A | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5435-6403C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47883926 | ||||||
chr3:47884148
|
A | G | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5435-6625T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47884148 | ||||||
chr3:47884273
|
G | T | 2 | a0012c0013t0011g0222a0017c0028t0002g0224 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.5435-6750C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47884273 | ||||||
chr3:47884493
|
G | T | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.5435-6970C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47884493 | ||||||
chr3:47884607
|
A | T | 1 | a0009c0009t0002g0048 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5435-7084T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47884607 | ||||||
chr3:47884673
|
C | T | 10 | a0005c0005t0003g0114a0005c0005t0003g0115a0005c0005t0003g0117others(7): Show | 10 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.5435-7150G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47884673 | ||||||
chr3:47884774
|
T | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0171a0001c0001t0026g0165 | 3 | HG01169.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5435-7251A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47884774 | ||||||
chr3:47885244
|
C | T | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5435-7721G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885244 | ||||||
chr3:47885367
|
C | CATCA | 92 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(89): Show | 92 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.5435-7848_5435-784 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885367 | ||||||
chr3:47885367
|
CATCA | C | 6 | a0001c0001t0001g0147a0002c0002t0002g0035a0012c0013t0011g0002others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.5435-7848_5435-784 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885367 | ||||||
chr3:47885367
|
CATCAATC others(5): Show |
C | 29 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(26): Show | 29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.5435-7856_5435-784 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885367 | ||||||
chr3:47885396
|
ATCAAT | A | 9 | a0002c0002t0002g0052a0002c0002t0002g0089a0002c0002t0002g0090others(6): Show | 9 | HG02015.hp2 NA18747.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.5435-7878_5435-787 others(9): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885396 | ||||||
chr3:47885737
|
T | C | 2 | a0002c0002t0002g0030a0002c0002t0002g0034 | 2 | NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.5435-8214A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885737 | ||||||
chr3:47885792
|
C | T | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.5435-8269G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885792 | ||||||
chr3:47885903
|
C | T | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5435-8380G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885903 | ||||||
chr3:47885965
|
T | C | 1 | a0002c0002t0002g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.5435-8442A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885965 | ||||||
chr3:47885994
|
T | C | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.5435-8471A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885994 | ||||||
chr3:47886070
|
T | C | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5435-8547A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47886070 | ||||||
chr3:47886342
|
C | T | 1 | a0022c0026t0015g0148 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.5435-8819G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47886342 | ||||||
chr3:47886486
|
G | A | 4 | a0007c0008t0007g0131a0007c0008t0007g0149a0007c0008t0007g0152others(1): Show | 4 | HG01891.hp1 HG02970.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.5435-8963C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47886486 | ||||||
chr3:47886677
|
C | T | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.5435-9154G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47886677 | ||||||
chr3:47887212
|
G | T | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.5435-9689C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47887212 | ||||||
chr3:47887225
|
C | A | 1 | a0002c0002t0002g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.5435-9702G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47887225 | ||||||
chr3:47887226
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5435-9703G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47887226 | ||||||
chr3:47887262
|
T | G | 1 | a0009c0009t0002g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5435-9739A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47887262 | ||||||
chr3:47887296
|
T | C | 123 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(120): Show | 124 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.5435-9773A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47887296 | ||||||
chr3:47887424
|
A | T | 1 | a0005c0005t0003g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5435-9901T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47887424 | ||||||
chr3:47887524
|
T | C | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.5435-10001A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47887524 | ||||||
chr3:47887716
|
A | T | 1 | a0004c0004t0021g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.5435-10193T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47887716 | ||||||
chr3:47888120
|
C | G | 8 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(5): Show | 8 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.5435-10597G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888120 | ||||||
chr3:47888179
|
A | G | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5435-10656T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888179 | ||||||
chr3:47888187
|
C | A | 1 | a0001c0001t0017g0135 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5435-10664G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888187 | ||||||
chr3:47888206
|
C | T | 10 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(7): Show | 10 | HG01934.hp1 HG02040.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.5435-10683G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888206 | ||||||
chr3:47888215
|
C | T | 1 | a0004c0004t0005g0085 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.5435-10692G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888215 | ||||||
chr3:47888245
|
A | G | 31 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0010others(28): Show | 31 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.5435-10722T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888245 | ||||||
chr3:47888436
|
C | G | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5435-10913G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888436 | ||||||
chr3:47888438
|
C | T | 1 | a0004c0004t0012g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5435-10915G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888438 | ||||||
chr3:47888457
|
G | A | 1 | a0002c0002t0006g0028 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.5435-10934C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888457 | ||||||
chr3:47888459
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.5435-10936T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888459 | ||||||
chr3:47888465
|
C | T | 81 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(78): Show | 82 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.5435-10942G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888465 | ||||||
chr3:47888550
|
G | C | 1 | a0005c0005t0003g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5435-11027C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888550 | ||||||
chr3:47888930
|
C | G | 121 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(118): Show | 122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.5435-11407G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888930 | ||||||
chr3:47889299
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5435-11776A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47889299 | ||||||
chr3:47889334
|
C | T | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5435-11811G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47889334 | ||||||
chr3:47889594
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | NA18940.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.5435-12071C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47889594 | ||||||
chr3:47889875
|
CCTCCATA others(18): Show |
C | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5435-12377_5435-12 others(31): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47889875 | ||||||
chr3:47889927
|
T | C | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5435-12404A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47889927 | ||||||
chr3:47890037
|
T | C | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5435-12514A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47890037 | ||||||
chr3:47890283
|
C | T | 2 | a0001c0001t0009g0166a0001c0001t0009g0167 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5434+12667G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47890283 | ||||||
chr3:47890489
|
T | C | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5434+12461A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47890489 | ||||||
chr3:47890494
|
C | A | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.5434+12456G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47890494 | ||||||
chr3:47890570
|
T | C | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5434+12380A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47890570 | ||||||
chr3:47890784
|
C | T | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.5434+12166G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47890784 | ||||||
chr3:47890886
|
C | G | 7 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(4): Show | 7 | NA18967.hp1 NA18969.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.5434+12064G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47890886 | ||||||
chr3:47891083
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5434+11867T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47891083 | ||||||
chr3:47891348
|
T | A | 1 | a0006c0006t0002g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.5434+11602A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47891348 | ||||||
chr3:47891504
|
A | C | 1 | a0002c0002t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5434+11446T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47891504 | ||||||
chr3:47891848
|
G | A | 4 | a0002c0002t0002g0057a0002c0002t0002g0058a0002c0002t0002g0125others(1): Show | 4 | HG02559.hp1 HG02976.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.5434+11102C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47891848 | ||||||
chr3:47891937
|
G | T | 1 | a0001c0001t0001g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.5434+11013C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47891937 | ||||||
chr3:47892140
|
C | T | 10 | a0005c0005t0003g0114a0005c0005t0003g0115a0005c0005t0003g0117others(7): Show | 10 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.5434+10810G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47892140 | ||||||
chr3:47892358
|
T | A | 1 | a0001c0001t0001g0127 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5434+10592A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47892358 | ||||||
chr3:47892398
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.5434+10552A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47892398 | ||||||
chr3:47892412
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5434+10538G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47892412 | ||||||
chr3:47892452
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.5434+10498G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47892452 | ||||||
chr3:47892718
|
C | G | 1 | a0002c0002t0002g0014 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.5434+10232G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47892718 | ||||||
chr3:47893026
|
T | TA | 102 | a0001c0001t0001g0169a0001c0001t0001g0173a0001c0001t0001g0195others(99): Show | 103 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.5434+9923dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893026 | ||||||
chr3:47893026
|
T | TAA | 8 | a0002c0002t0002g0010a0002c0002t0002g0033a0002c0002t0002g0091others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.5434+9922_5434+992 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893026 | ||||||
chr3:47893050
|
C | A | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5434+9900G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893050 | ||||||
chr3:47893258
|
C | T | 1 | a0005c0005t0003g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5434+9692G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893258 | ||||||
chr3:47893500
|
C | T | 3 | a0001c0001t0001g0134a0001c0001t0001g0145a0001c0001t0001g0146 | 3 | HG00639.hp2 HG00733.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.5434+9450G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893500 | ||||||
chr3:47893672
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5434+9278A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893672 | ||||||
chr3:47893759
|
CT | C | 17 | a0001c0001t0001g0154a0001c0001t0001g0158a0001c0001t0001g0168others(14): Show | 17 | HG00099.hp2 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.5434+9190delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893759 | ||||||
chr3:47893774
|
T | A | 11 | a0002c0002t0002g0021a0002c0002t0002g0024a0002c0002t0002g0025others(8): Show | 11 | HG00099.hp2 HG01074.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.5434+9176A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893774 | ||||||
chr3:47893775
|
A | T | 2 | a0001c0001t0009g0166a0001c0001t0009g0167 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5434+9175T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893775 | ||||||
chr3:47893783
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.5434+9167C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893783 | ||||||
chr3:47893813
|
G | T | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.5434+9137C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893813 | ||||||
chr3:47893933
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.5434+9017G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893933 | ||||||
chr3:47893976
|
C | A | 1 | a0001c0001t0001g0214 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.5434+8974G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893976 | ||||||
chr3:47894074
|
A | G | 1 | a0002c0002t0002g0027 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.5434+8876T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894074 | ||||||
chr3:47894087
|
G | C | 2 | a0012c0013t0011g0222a0017c0028t0002g0224 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.5434+8863C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894087 | ||||||
chr3:47894201
|
T | C | 1 | a0002c0011t0002g0087 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5434+8749A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894201 | ||||||
chr3:47894302
|
G | A | 2 | a0001c0001t0009g0166a0001c0001t0009g0167 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5434+8648C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894302 | ||||||
chr3:47894478
|
G | A | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5434+8472C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894478 | ||||||
chr3:47894562
|
G | A | 8 | a0002c0002t0002g0045a0002c0002t0002g0055a0002c0002t0002g0056others(5): Show | 8 | HG02559.hp1 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.5434+8388C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894562 | ||||||
chr3:47894600
|
G | GA | 36 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0134others(33): Show | 36 | HG00544.hp1 HG00609.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.5434+8349dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894600 | ||||||
chr3:47894609
|
T | C | 1 | a0003c0003t0003g0103 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5434+8341A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894609 | ||||||
chr3:47894716
|
G | A | 1 | a0007c0008t0007g0131 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5434+8234C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894716 | ||||||
chr3:47895021
|
C | CA | 35 | a0001c0001t0001g0229a0003c0003t0003g0095a0003c0003t0003g0098others(32): Show | 35 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.5434+7928dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47895021 | ||||||
chr3:47895181
|
T | C | 172 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(169): Show | 173 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(170): Show |
intron_variant | MODIFIER | c.5434+7769A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47895181 | ||||||
chr3:47895530
|
C | T | 2 | a0004c0004t0012g0049a0004c0004t0012g0050 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.5434+7420G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47895530 | ||||||
chr3:47895582
|
T | C | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.5434+7368A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47895582 | ||||||
chr3:47896144
|
G | A | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5434+6806C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47896144 | ||||||
chr3:47896864
|
G | C | 120 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(117): Show | 121 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.5434+6086C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47896864 | ||||||
chr3:47896895
|
G | T | 29 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(26): Show | 29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.5434+6055C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47896895 | ||||||
chr3:47897446
|
C | T | 1 | a0004c0004t0005g0086 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.5434+5504G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897446 | ||||||
chr3:47897528
|
T | C | 26 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(23): Show | 26 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.5434+5422A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897528 | ||||||
chr3:47897704
|
C | T | 3 | a0006c0006t0002g0074a0006c0006t0002g0075a0006c0006t0002g0076 | 3 | HG02602.hp1 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.5434+5246G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897704 | ||||||
chr3:47897891
|
G | A | 1 | a0008c0010t0008g0111 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5434+5059C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897891 | ||||||
chr3:47897950
|
G | GA | 13 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(10): Show | 13 | HG01934.hp1 HG02071.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.5434+4999dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897950 | ||||||
chr3:47897951
|
A | G | 15 | a0001c0001t0010g0178a0003c0003t0003g0095a0003c0003t0003g0098others(12): Show | 15 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.5434+4999T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897951 | ||||||
chr3:47897952
|
A | G | 2 | a0003c0003t0003g0110a0020c0022t0002g0088 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5434+4998T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897952 | ||||||
chr3:47897953
|
A | G | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5434+4997T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897953 | ||||||
chr3:47897959
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5434+4991T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897959 | ||||||
chr3:47898136
|
G | A | 91 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(88): Show | 92 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.5434+4814C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47898136 | ||||||
chr3:47898426
|
C | T | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5434+4524G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47898426 | ||||||
chr3:47898494
|
C | T | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5434+4456G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47898494 | ||||||
chr3:47898495
|
C | T | 29 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(26): Show | 29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.5434+4455G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47898495 | ||||||
chr3:47898500
|
C | CA | 5 | a0001c0001t0001g0159a0001c0001t0001g0198a0001c0001t0024g0213others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.5434+4449dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47898500 | ||||||
chr3:47898929
|
C | T | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5434+4021G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47898929 | ||||||
chr3:47899239
|
G | A | 1 | a0002c0002t0002g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.5434+3711C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47899239 | ||||||
chr3:47899744
|
G | A | 1 | a0006c0006t0002g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.5434+3206C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47899744 | ||||||
chr3:47900126
|
T | C | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.5434+2824A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47900126 | ||||||
chr3:47900304
|
T | C | 1 | a0004c0004t0021g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.5434+2646A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47900304 | ||||||
chr3:47900858
|
A | G | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5434+2092T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47900858 | ||||||
chr3:47901072
|
C | T | 10 | a0005c0005t0003g0114a0005c0005t0003g0115a0005c0005t0003g0117others(7): Show | 10 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.5434+1878G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47901072 | ||||||
chr3:47901184
|
A | G | 1 | a0002c0002t0004g0017 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.5434+1766T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47901184 | ||||||
chr3:47901442
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.5434+1508C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47901442 | ||||||
chr3:47901759
|
C | G | 1 | a0005c0005t0003g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5434+1191G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47901759 | ||||||
chr3:47902123
|
C | T | 16 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(13): Show | 16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.5434+827G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902123 | ||||||
chr3:47902371
|
T | C | 91 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(88): Show | 92 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.5434+579A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902371 | ||||||
chr3:47902415
|
C | T | 1 | a0002c0002t0002g0036 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.5434+535G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902415 | ||||||
chr3:47902430
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.5434+520G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902430 | ||||||
chr3:47902673
|
C | CA | 38 | a0001c0001t0001g0042a0001c0001t0001g0138a0001c0001t0001g0141others(35): Show | 38 | HG00597.hp1 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.5434+276dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902673 | ||||||
chr3:47902673
|
C | CAA | 36 | a0001c0001t0001g0181a0001c0001t0001g0198a0001c0001t0001g0207others(33): Show | 36 | HG00673.hp2 HG00735.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.5434+275_5434+276d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902673 | ||||||
chr3:47902673
|
C | CAAA | 35 | a0001c0001t0001g0154a0001c0001t0001g0188a0002c0002t0002g0001others(32): Show | 36 | HG00099.hp2 HG00544.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.5434+274_5434+276d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902673 | ||||||
chr3:47902673
|
C | CAAAA | 16 | a0002c0002t0002g0034a0002c0002t0002g0052a0002c0002t0002g0057others(13): Show | 16 | HG00280.hp2 HG01123.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.5434+273_5434+276d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902673 | ||||||
chr3:47902673
|
CA | C | 5 | a0001c0001t0001g0041a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG00673.hp1 HG02486.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.5434+276delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902673 | ||||||
chr3:47902673
|
CAAAAAAA others(4): Show |
C | 1 | a0027c0021t0002g0011 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.5434+266_5434+276d others(13): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902673 | ||||||
chr3:47903146
|
AG | A | 121 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(118): Show | 122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.5384-147delC | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47903146 | ||||||
chr3:47903156
|
C | T | 1 | a0022c0026t0015g0148 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.5384-156G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47903156 | ||||||
chr3:47903254
|
C | A | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5384-254G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47903254 | ||||||
chr3:47903532
|
C | CA | 22 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0191others(19): Show | 22 | HG00741.hp1 HG01934.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.5384-533dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47903532 | ||||||
chr3:47903532
|
CA | C | 5 | a0001c0001t0001g0214a0002c0002t0002g0004a0002c0002t0002g0005others(2): Show | 5 | HG01981.hp2 NA18952.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.5384-533delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47903532 | ||||||
chr3:47903572
|
G | C | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5384-572C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47903572 | ||||||
chr3:47903661
|
A | C | 1 | a0002c0002t0004g0017 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.5384-661T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47903661 | ||||||
chr3:47904043
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5384-1043T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47904043 | ||||||
chr3:47904235
|
A | G | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5384-1235T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47904235 | ||||||
chr3:47904327
|
A | T | 92 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(89): Show | 93 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.5384-1327T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47904327 | ||||||
chr3:47904461
|
G | A | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5384-1461C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47904461 | ||||||
chr3:47904582
|
T | G | 1 | a0001c0001t0010g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5384-1582A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47904582 | ||||||
chr3:47905218
|
T | C | 81 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(78): Show | 82 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.5384-2218A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905218 | ||||||
chr3:47905343
|
A | G | 1 | a0002c0002t0002g0036 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.5384-2343T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905343 | ||||||
chr3:47905479
|
G | A | 6 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(3): Show | 6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.5384-2479C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905479 | ||||||
chr3:47905524
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.5384-2524T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905524 | ||||||
chr3:47905545
|
C | A | 1 | a0018c0023t0005g0053 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.5384-2545G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905545 | ||||||
chr3:47905548
|
A | C | 18 | a0001c0001t0001g0138a0001c0001t0001g0159a0001c0001t0001g0186others(15): Show | 18 | HG00544.hp2 HG01891.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.5384-2548T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905548 | ||||||
chr3:47905551
|
A | C | 1 | a0012c0013t0011g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5384-2551T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905551 | ||||||
chr3:47905558
|
C | A | 1 | a0001c0001t0002g0150 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.5384-2558G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905558 | ||||||
chr3:47905688
|
G | A | 1 | a0005c0005t0020g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5384-2688C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905688 | ||||||
chr3:47905691
|
AC | A | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.5384-2692delG | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905691 | ||||||
chr3:47905694
|
A | T | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.5384-2694T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905694 | ||||||
chr3:47905734
|
C | T | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG01074.hp1 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.5384-2734G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905734 | ||||||
chr3:47905855
|
G | A | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5384-2855C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905855 | ||||||
chr3:47906031
|
A | C | 3 | a0006c0006t0002g0074a0006c0006t0002g0075a0006c0006t0002g0076 | 3 | HG02602.hp1 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.5383+3007T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906031 | ||||||
chr3:47906084
|
C | CA | 31 | a0001c0001t0001g0042a0001c0001t0001g0158a0001c0001t0001g0191others(28): Show | 31 | HG00738.hp1 HG01109.hp2 HG01516.hp2 others(28): Show |
intron_variant | MODIFIER | c.5383+2953dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906084 | ||||||
chr3:47906084
|
C | CAA | 7 | a0003c0003t0003g0107a0005c0005t0003g0114a0005c0005t0003g0115others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.5383+2952_5383+295 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906084 | ||||||
chr3:47906247
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5383+2791G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906247 | ||||||
chr3:47906596
|
TC | T | 2 | a0002c0002t0004g0015a0002c0002t0004g0016 | 2 | NA19005.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.5383+2441delG | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906596 | ||||||
chr3:47906623
|
C | T | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.5383+2415G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906623 | ||||||
chr3:47906795
|
T | TA | 32 | a0001c0001t0001g0147a0002c0002t0014g0065a0003c0003t0003g0095others(29): Show | 32 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.5383+2242dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906795 | ||||||
chr3:47906808
|
A | C | 1 | a0002c0002t0002g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.5383+2230T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906808 | ||||||
chr3:47906874
|
G | T | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.5383+2164C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906874 | ||||||
chr3:47906985
|
A | G | 225 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(222): Show | 226 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(223): Show |
intron_variant | MODIFIER | c.5383+2053T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906985 | ||||||
chr3:47907077
|
C | T | 2 | a0001c0001t0009g0166a0001c0001t0009g0167 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5383+1961G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47907077 | ||||||
chr3:47907087
|
G | A | 1 | a0004c0004t0005g0086 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.5383+1951C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47907087 | ||||||
chr3:47907420
|
T | A | 4 | a0001c0007t0001g0219a0004c0004t0005g0223a0005c0005t0003g0114others(1): Show | 4 | HG02040.hp2 HG02071.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.5383+1618A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47907420 | ||||||
chr3:47907590
|
A | G | 1 | a0002c0002t0002g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.5383+1448T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47907590 | ||||||
chr3:47908048
|
G | GT | 81 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(78): Show | 82 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.5383+989dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47908048 | ||||||
chr3:47908185
|
C | A | 1 | a0001c0001t0002g0150 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.5383+853G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47908185 | ||||||
chr3:47908229
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5383+809G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47908229 | ||||||
chr3:47908841
|
C | A | 1 | a0018c0023t0005g0053 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.5383+197G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47908841 | ||||||
chr3:47912447
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2000-26G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 8/20 | chr3 | 47912447 | ||||||
chr3:47913836
|
A | G | 1 | a0017c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1999+981T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 8/20 | chr3 | 47913836 | ||||||
chr3:47913977
|
A | T | 4 | a0001c0007t0001g0218a0001c0007t0001g0219a0001c0007t0001g0220others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1999+840T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 8/20 | chr3 | 47913977 | ||||||
chr3:47914511
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1999+306A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 8/20 | chr3 | 47914511 | ||||||
chr3:47915016
|
T | C | 81 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(78): Show | 82 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1877-77A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915016 | ||||||
chr3:47915035
|
G | A | 8 | a0001c0001t0001g0157a0001c0001t0001g0162a0001c0001t0001g0163others(5): Show | 8 | HG00544.hp1 HG00609.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1877-96C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915035 | ||||||
chr3:47915070
|
G | A | 1 | a0002c0002t0004g0003 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1877-131C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915070 | ||||||
chr3:47915174
|
T | C | 1 | a0002c0020t0002g0054 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1877-235A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915174 | ||||||
chr3:47915179
|
C | T | 4 | a0002c0002t0002g0052a0002c0002t0002g0094a0002c0002t0002g0118others(1): Show | 4 | HG02015.hp2 NA18747.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1877-240G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915179 | ||||||
chr3:47915185
|
C | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0156 | 2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1877-246G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915185 | ||||||
chr3:47915202
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1877-263G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915202 | ||||||
chr3:47915382
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1877-443G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915382 | ||||||
chr3:47915435
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1877-496A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915435 | ||||||
chr3:47915541
|
C | T | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1876+410G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915541 | ||||||
chr3:47915629
|
G | C | 4 | a0002c0002t0002g0052a0002c0002t0002g0094a0002c0002t0002g0118others(1): Show | 4 | HG02015.hp2 NA18747.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1876+322C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915629 | ||||||
chr3:47915725
|
T | C | 2 | a0002c0002t0002g0029a0002c0002t0002g0032 | 2 | HG00544.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1876+226A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915725 | ||||||
chr3:47915799
|
G | A | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1876+152C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915799 | ||||||
chr3:47915867
|
T | G | 1 | a0002c0002t0014g0065 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1876+84A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915867 | ||||||
chr3:47917266
|
G | A | 1 | a0002c0002t0002g0070 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.653-92C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47917266 | ||||||
chr3:47917518
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.653-344C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47917518 | ||||||
chr3:47917544
|
G | T | 1 | a0001c0001t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.653-370C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47917544 | ||||||
chr3:47917585
|
C | CA | 8 | a0001c0001t0001g0043a0001c0001t0001g0127a0001c0001t0001g0136others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.653-412dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47917585 | ||||||
chr3:47917585
|
CA | C | 121 | a0001c0001t0001g0216a0002c0002t0002g0001a0002c0002t0002g0004others(118): Show | 122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.653-412delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47917585 | ||||||
chr3:47917605
|
G | A | 1 | a0004c0004t0012g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.653-431C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47917605 | ||||||
chr3:47918196
|
C | G | 1 | a0002c0002t0002g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.652+523G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47918196 | ||||||
chr3:47918280
|
A | G | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.652+439T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47918280 | ||||||
chr3:47918479
|
GA | G | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.652+239delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47918479 | ||||||
chr3:47918485
|
A | AAT | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.652+232_652+233dup others(2): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47918485 | ||||||
chr3:47918487
|
T | A | 11 | a0001c0007t0001g0219a0005c0005t0003g0114a0005c0005t0003g0115others(8): Show | 11 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.652+232A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47918487 | ||||||
chr3:47919021
|
T | A | 81 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(78): Show | 82 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.530-180A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919021 | ||||||
chr3:47919040
|
T | C | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.530-199A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919040 | ||||||
chr3:47919119
|
G | C | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.530-278C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919119 | ||||||
chr3:47919142
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.530-301G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919142 | ||||||
chr3:47919143
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.530-302C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919143 | ||||||
chr3:47919210
|
C | T | 2 | a0007c0008t0007g0131a0007c0008t0007g0226 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.530-369G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919210 | ||||||
chr3:47919285
|
C | A | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.530-444G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919285 | ||||||
chr3:47919356
|
G | A | 3 | a0008c0010t0008g0111a0008c0010t0008g0112a0008c0010t0008g0113 | 3 | HG00738.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.530-515C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919356 | ||||||
chr3:47919410
|
C | T | 4 | a0001c0007t0001g0218a0001c0007t0001g0219a0001c0007t0001g0220others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-569G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919410 | ||||||
chr3:47919443
|
G | T | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.530-602C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919443 | ||||||
chr3:47919530
|
G | C | 1 | a0018c0023t0005g0053 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.530-689C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919530 | ||||||
chr3:47919541
|
C | T | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.530-700G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919541 | ||||||
chr3:47919569
|
A | G | 1 | a0002c0002t0002g0025 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.530-728T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919569 | ||||||
chr3:47919601
|
C | T | 3 | a0002c0002t0002g0123a0002c0011t0002g0073a0002c0011t0002g0087 | 3 | HG00639.hp1 HG00733.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.530-760G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919601 | ||||||
chr3:47919916
|
T | TTTG | 4 | a0001c0001t0001g0134a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | HG00639.hp2 HG00733.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-1078_530-1076d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919916 | ||||||
chr3:47919916
|
TTTG | T | 122 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(119): Show | 123 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.530-1078_530-1076d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919916 | ||||||
chr3:47920114
|
G | C | 47 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(44): Show | 47 | HG00544.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.530-1273C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920114 | ||||||
chr3:47920136
|
A | C | 7 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0021others(4): Show | 7 | HG00099.hp2 HG00673.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.530-1295T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920136 | ||||||
chr3:47920191
|
G | C | 1 | a0003c0003t0003g0102 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.530-1350C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920191 | ||||||
chr3:47920253
|
G | T | 1 | a0002c0002t0002g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.530-1412C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920253 | ||||||
chr3:47920354
|
G | A | 9 | a0002c0002t0002g0052a0002c0002t0002g0089a0002c0002t0002g0090others(6): Show | 9 | HG02015.hp2 NA18747.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.529+1411C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920354 | ||||||
chr3:47920542
|
T | C | 1 | a0004c0004t0021g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.529+1223A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920542 | ||||||
chr3:47920544
|
GT | G | 159 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0126others(156): Show | 160 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.529+1220delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920544 | ||||||
chr3:47920544
|
GTT | G | 13 | a0001c0001t0001g0159a0001c0001t0001g0173a0001c0001t0001g0174others(10): Show | 13 | HG00597.hp1 HG02071.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.529+1219_529+1220d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920544 | ||||||
chr3:47920568
|
T | A | 14 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(11): Show | 14 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.529+1197A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920568 | ||||||
chr3:47920702
|
C | G | 1 | a0004c0004t0012g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.529+1063G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920702 | ||||||
chr3:47920945
|
C | G | 1 | a0004c0004t0012g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.529+820G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920945 | ||||||
chr3:47921542
|
C | A | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.529+223G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47921542 | ||||||
chr3:47922565
|
TA | T | 122 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(119): Show | 123 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.416-688delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47922565 | ||||||
chr3:47922764
|
G | A | 1 | a0001c0001t0010g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.416-886C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47922764 | ||||||
chr3:47922766
|
A | G | 1 | a0017c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.416-888T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47922766 | ||||||
chr3:47922818
|
G | A | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.416-940C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47922818 | ||||||
chr3:47922921
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.416-1043C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47922921 | ||||||
chr3:47922974
|
C | T | 1 | a0022c0026t0015g0148 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.416-1096G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47922974 | ||||||
chr3:47922999
|
G | A | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.416-1121C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47922999 | ||||||
chr3:47923024
|
T | G | 9 | a0002c0002t0002g0052a0002c0002t0002g0089a0002c0002t0002g0090others(6): Show | 9 | HG02015.hp2 NA18747.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.416-1146A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47923024 | ||||||
chr3:47923347
|
T | C | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.416-1469A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47923347 | ||||||
chr3:47923623
|
T | TA | 12 | a0001c0001t0001g0139a0001c0001t0001g0163a0001c0001t0001g0164others(9): Show | 12 | HG00733.hp1 HG00741.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.416-1746dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47923623 | ||||||
chr3:47923638
|
C | A | 4 | a0001c0007t0001g0218a0001c0007t0001g0219a0002c0002t0002g0092others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-1760G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47923638 | ||||||
chr3:47923685
|
G | A | 16 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(13): Show | 16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.416-1807C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47923685 | ||||||
chr3:47924715
|
T | C | 2 | a0004c0004t0012g0049a0004c0004t0012g0050 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.416-2837A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47924715 | ||||||
chr3:47924816
|
A | AT | 126 | a0001c0001t0001g0184a0002c0002t0002g0001a0002c0002t0002g0004others(123): Show | 127 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.416-2939dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47924816 | ||||||
chr3:47924959
|
C | T | 120 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(117): Show | 121 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.416-3081G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47924959 | ||||||
chr3:47925270
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.415+2958C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47925270 | ||||||
chr3:47925583
|
G | A | 1 | a0003c0003t0003g0095 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.415+2645C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47925583 | ||||||
chr3:47925629
|
A | G | 16 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(13): Show | 16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.415+2599T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47925629 | ||||||
chr3:47925713
|
G | C | 2 | a0004c0004t0012g0049a0004c0004t0012g0050 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.415+2515C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47925713 | ||||||
chr3:47925747
|
T | C | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.415+2481A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47925747 | ||||||
chr3:47925824
|
G | A | 1 | a0017c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.415+2404C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47925824 | ||||||
chr3:47925924
|
G | A | 1 | a0002c0002t0002g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.415+2304C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47925924 | ||||||
chr3:47926076
|
G | A | 1 | a0002c0002t0002g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.415+2152C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47926076 | ||||||
chr3:47926253
|
G | A | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.415+1975C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47926253 | ||||||
chr3:47926287
|
G | A | 1 | a0002c0002t0004g0017 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.415+1941C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47926287 | ||||||
chr3:47926580
|
G | A | 16 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(13): Show | 16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.415+1648C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47926580 | ||||||
chr3:47926811
|
C | T | 1 | a0001c0001t0010g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.415+1417G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47926811 | ||||||
chr3:47926881
|
T | C | 6 | a0001c0001t0001g0042a0001c0001t0001g0043a0002c0002t0006g0026others(3): Show | 6 | HG01074.hp2 HG01346.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.415+1347A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47926881 | ||||||
chr3:47927022
|
T | C | 1 | a0008c0010t0008g0111 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.415+1206A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47927022 | ||||||
chr3:47927062
|
G | C | 15 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(12): Show | 15 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.415+1166C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47927062 | ||||||
chr3:47927158
|
C | CA | 87 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0173others(84): Show | 87 | HG00544.hp2 HG00597.hp2 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.415+1069dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47927158 | ||||||
chr3:47927158
|
C | CAA | 43 | a0002c0002t0002g0001a0002c0002t0002g0025a0002c0002t0002g0030others(40): Show | 44 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.415+1068_415+1069d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47927158 | ||||||
chr3:47927241
|
G | A | 230 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.415+987C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47927241 | ||||||
chr3:47927507
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.415+721G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47927507 | ||||||
chr3:47927822
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.415+406A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47927822 | ||||||
chr3:47927855
|
GT | G | 2 | a0013c0012t0002g0071a0013c0012t0002g0078 | 2 | HG04115.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.415+372delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47927855 | ||||||
chr3:47928577
|
C | T | 1 | a0001c0001t0026g0165 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.293-227G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47928577 | ||||||
chr3:47928619
|
C | T | 121 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(118): Show | 122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.293-269G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47928619 | ||||||
chr3:47928647
|
T | C | 1 | a0002c0002t0002g0022 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.293-297A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47928647 | ||||||
chr3:47928812
|
C | T | 1 | a0004c0004t0005g0085 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.293-462G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47928812 | ||||||
chr3:47928840
|
G | A | 4 | a0003c0003t0003g0102a0003c0003t0003g0104a0003c0003t0003g0108others(1): Show | 4 | HG02922.hp1 HG02965.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-490C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47928840 | ||||||
chr3:47929312
|
C | A | 1 | a0005c0005t0003g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.293-962G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929312 | ||||||
chr3:47929376
|
G | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0145a0001c0001t0001g0146 | 3 | HG00639.hp2 HG00733.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.293-1026C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929376 | ||||||
chr3:47929563
|
A | G | 8 | a0002c0002t0002g0045a0002c0002t0002g0055a0002c0002t0002g0056others(5): Show | 8 | HG02559.hp1 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-1213T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929563 | ||||||
chr3:47929627
|
C | CA | 24 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0132others(21): Show | 24 | HG00609.hp1 HG00673.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.293-1278dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929627 | ||||||
chr3:47929627
|
CA | C | 34 | a0001c0001t0001g0042a0001c0001t0001g0171a0001c0001t0001g0185others(31): Show | 34 | HG00597.hp2 HG01123.hp2 HG02145.hp1 others(31): Show |
intron_variant | MODIFIER | c.293-1278delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929627 | ||||||
chr3:47929627
|
CAA | C | 49 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0012others(46): Show | 50 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.293-1279_293-1278d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929627 | ||||||
chr3:47929627
|
CAAA | C | 37 | a0002c0002t0002g0005a0002c0002t0002g0010a0002c0002t0002g0013others(34): Show | 37 | HG00099.hp2 HG00544.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.293-1280_293-1278d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929627 | ||||||
chr3:47929627
|
CAAAA | C | 6 | a0004c0004t0005g0085a0004c0004t0005g0086a0004c0004t0005g0223others(3): Show | 6 | HG02040.hp2 HG02071.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-1281_293-1278d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929627 | ||||||
chr3:47929627
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0170 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.293-1289_293-1278d others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929627 | ||||||
chr3:47929822
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.293-1472A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929822 | ||||||
chr3:47929958
|
A | G | 121 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(118): Show | 122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.293-1608T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929958 | ||||||
chr3:47930031
|
G | A | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.293-1681C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930031 | ||||||
chr3:47930124
|
G | A | 2 | a0002c0002t0002g0030a0002c0002t0002g0034 | 2 | NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.293-1774C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930124 | ||||||
chr3:47930125
|
C | T | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-1775G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930125 | ||||||
chr3:47930167
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.293-1817G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930167 | ||||||
chr3:47930174
|
G | A | 1 | a0017c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.293-1824C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930174 | ||||||
chr3:47930186
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.293-1836G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930186 | ||||||
chr3:47930308
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.293-1958C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930308 | ||||||
chr3:47930374
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.293-2024T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930374 | ||||||
chr3:47930414
|
C | T | 1 | a0026c0017t0002g0038 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.293-2064G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930414 | ||||||
chr3:47930459
|
A | C | 1 | a0012c0013t0011g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.293-2109T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930459 | ||||||
chr3:47930475
|
C | A | 124 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(121): Show | 125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.293-2125G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930475 | ||||||
chr3:47930789
|
C | T | 2 | a0003c0003t0003g0100a0015c0030t0025g0044 | 2 | HG02486.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.293-2439G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930789 | ||||||
chr3:47930877
|
G | A | 1 | a0002c0002t0006g0028 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.293-2527C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930877 | ||||||
chr3:47930885
|
C | A | 1 | a0002c0002t0006g0040 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.293-2535G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930885 | ||||||
chr3:47931595
|
C | T | 1 | a0028c0016t0006g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.293-3245G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47931595 | ||||||
chr3:47931596
|
G | A | 10 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(7): Show | 10 | HG01934.hp1 HG02040.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-3246C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47931596 | ||||||
chr3:47931656
|
A | AT | 82 | a0001c0001t0001g0129a0001c0001t0001g0196a0001c0001t0024g0213others(79): Show | 83 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.293-3307dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47931656 | ||||||
chr3:47931656
|
A | ATT | 8 | a0001c0001t0001g0197a0002c0002t0002g0055a0002c0002t0002g0061others(5): Show | 8 | HG01109.hp1 HG01169.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-3308_293-3307d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47931656 | ||||||
chr3:47931656
|
A | T | 1 | a0002c0002t0002g0094 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.293-3306T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47931656 | ||||||
chr3:47931705
|
A | G | 1 | a0017c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.293-3355T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47931705 | ||||||
chr3:47932124
|
T | A | 8 | a0002c0002t0002g0045a0002c0002t0002g0055a0002c0002t0002g0056others(5): Show | 8 | HG02559.hp1 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-3774A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47932124 | ||||||
chr3:47932260
|
A | G | 1 | a0001c0007t0001g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.293-3910T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47932260 | ||||||
chr3:47933002
|
A | C | 1 | a0001c0001t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.293-4652T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47933002 | ||||||
chr3:47933299
|
G | C | 1 | a0001c0001t0010g0205 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.293-4949C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47933299 | ||||||
chr3:47933450
|
T | C | 1 | a0002c0002t0002g0089 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.293-5100A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47933450 | ||||||
chr3:47933601
|
C | CT | 107 | a0001c0001t0001g0129a0001c0001t0001g0206a0001c0001t0001g0210others(104): Show | 108 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.293-5252dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47933601 | ||||||
chr3:47933601
|
C | CTT | 18 | a0002c0002t0002g0018a0002c0002t0002g0020a0002c0002t0002g0022others(15): Show | 18 | HG00673.hp2 HG00738.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-5253_293-5252d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47933601 | ||||||
chr3:47933701
|
C | A | 1 | a0001c0007t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.293-5351G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47933701 | ||||||
chr3:47933757
|
C | T | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.293-5407G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47933757 | ||||||
chr3:47934138
|
G | C | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.293-5788C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47934138 | ||||||
chr3:47934417
|
C | T | 2 | a0002c0002t0002g0020a0027c0021t0002g0011 | 2 | HG00597.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.293-6067G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47934417 | ||||||
chr3:47934655
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.293-6305G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47934655 | ||||||
chr3:47934714
|
T | C | 1 | a0023c0027t0001g0175 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.293-6364A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47934714 | ||||||
chr3:47934910
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.293-6560G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47934910 | ||||||
chr3:47934912
|
T | C | 29 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(26): Show | 29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.293-6562A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47934912 | ||||||
chr3:47934949
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0153a0001c0001t0002g0150 | 3 | HG01981.hp1 HG02135.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.293-6599G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47934949 | ||||||
chr3:47935321
|
C | T | 1 | a0006c0006t0002g0081 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.293-6971G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935321 | ||||||
chr3:47935524
|
T | C | 15 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(12): Show | 15 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.293-7174A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935524 | ||||||
chr3:47935792
|
C | G | 1 | a0001c0001t0001g0208 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.293-7442G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935792 | ||||||
chr3:47935808
|
G | A | 2 | a0002c0002t0002g0037a0002c0002t0002g0039 | 2 | HG02135.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.293-7458C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935808 | ||||||
chr3:47935844
|
C | A | 2 | a0012c0013t0011g0222a0017c0028t0002g0224 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.293-7494G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935844 | ||||||
chr3:47935875
|
G | A | 1 | a0008c0010t0008g0112 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.293-7525C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935875 | ||||||
chr3:47935939
|
C | CA | 7 | a0001c0001t0001g0145a0001c0001t0001g0172a0001c0001t0001g0208others(4): Show | 7 | HG00609.hp2 HG00733.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-7590dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935939 | ||||||
chr3:47935939
|
CA | C | 6 | a0001c0001t0001g0137a0001c0001t0001g0140a0002c0002t0002g0091others(3): Show | 6 | HG01891.hp2 HG02015.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-7590delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935939 | ||||||
chr3:47935956
|
A | T | 31 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0010others(28): Show | 31 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.293-7606T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935956 | ||||||
chr3:47935957
|
AT | A | 10 | a0005c0005t0003g0114a0005c0005t0003g0115a0005c0005t0003g0117others(7): Show | 10 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-7608delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935957 | ||||||
chr3:47936479
|
G | A | 1 | a0012c0013t0011g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.293-8129C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47936479 | ||||||
chr3:47936699
|
G | A | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-8349C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47936699 | ||||||
chr3:47936809
|
C | T | 1 | a0002c0002t0002g0063 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.293-8459G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47936809 | ||||||
chr3:47936921
|
A | G | 1 | a0002c0002t0014g0065 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.293-8571T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47936921 | ||||||
chr3:47936980
|
CA | C | 123 | a0001c0001t0001g0163a0001c0001t0001g0171a0002c0002t0002g0001others(120): Show | 124 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.293-8631delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47936980 | ||||||
chr3:47937583
|
T | A | 2 | a0008c0010t0008g0111a0008c0010t0008g0112 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.293-9233A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937583 | ||||||
chr3:47937618
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0201 | 2 | HG00609.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.293-9268A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937618 | ||||||
chr3:47937656
|
C | CT | 10 | a0001c0001t0001g0186a0001c0001t0001g0200a0001c0001t0001g0210others(7): Show | 10 | HG00673.hp1 HG01257.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.293-9307dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937656 | ||||||
chr3:47937656
|
CT | C | 25 | a0001c0001t0001g0179a0002c0002t0002g0030a0003c0003t0003g0095others(22): Show | 25 | HG01109.hp2 HG01934.hp1 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.293-9307delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937656 | ||||||
chr3:47937656
|
CTT | C | 95 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(92): Show | 96 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.293-9308_293-9307d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937656 | ||||||
chr3:47937656
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0138 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.293-9316_293-9307d others(12): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937656 | ||||||
chr3:47937669
|
T | G | 1 | a0001c0001t0001g0138 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.293-9319A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937669 | ||||||
chr3:47937745
|
T | A | 6 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(3): Show | 6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-9395A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937745 | ||||||
chr3:47937749
|
C | T | 1 | a0012c0013t0011g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.293-9399G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937749 | ||||||
chr3:47937806
|
C | T | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.293-9456G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937806 | ||||||
chr3:47938040
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.293-9690G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47938040 | ||||||
chr3:47938119
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.293-9769G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47938119 | ||||||
chr3:47938452
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.293-10102G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47938452 | ||||||
chr3:47938461
|
C | A | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.293-10111G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47938461 | ||||||
chr3:47938601
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.293-10251C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47938601 | ||||||
chr3:47938685
|
A | G | 29 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(26): Show | 29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.293-10335T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47938685 | ||||||
chr3:47938816
|
A | G | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.293-10466T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47938816 | ||||||
chr3:47938992
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.293-10642A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47938992 | ||||||
chr3:47939048
|
T | A | 1 | a0002c0002t0002g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.293-10698A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939048 | ||||||
chr3:47939166
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.293-10816G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939166 | ||||||
chr3:47939325
|
TTTCA | T | 26 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(23): Show | 26 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.293-10979_293-1097 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939325 | ||||||
chr3:47939341
|
G | A | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-10991C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939341 | ||||||
chr3:47939405
|
C | T | 2 | a0002c0002t0002g0069a0002c0002t0002g0231 | 2 | HG00741.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.293-11055G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939405 | ||||||
chr3:47939499
|
A | C | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-11149T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939499 | ||||||
chr3:47939589
|
T | A | 1 | a0002c0002t0002g0089 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.293-11239A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939589 | ||||||
chr3:47939590
|
A | T | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.293-11240T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939590 | ||||||
chr3:47939684
|
C | G | 1 | a0012c0013t0011g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.293-11334G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939684 | ||||||
chr3:47939709
|
GT | G | 128 | a0001c0001t0001g0158a0001c0001t0001g0168a0001c0001t0001g0169others(125): Show | 129 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.293-11360delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939709 | ||||||
chr3:47939736
|
C | T | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-11386G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939736 | ||||||
chr3:47939784
|
C | G | 1 | a0001c0001t0001g0140 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.293-11434G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939784 | ||||||
chr3:47939867
|
G | A | 1 | a0002c0002t0002g0032 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.293-11517C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939867 | ||||||
chr3:47940068
|
C | A | 1 | a0001c0007t0001g0221 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.293-11718G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47940068 | ||||||
chr3:47940407
|
A | T | 1 | a0001c0001t0001g0139 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.293-12057T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47940407 | ||||||
chr3:47940475
|
T | C | 2 | a0012c0013t0011g0222a0017c0028t0002g0224 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.293-12125A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47940475 | ||||||
chr3:47941220
|
C | CA | 14 | a0001c0001t0001g0042a0001c0001t0001g0128a0001c0001t0001g0153others(11): Show | 14 | HG01074.hp1 HG01257.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.293-12871dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941220 | ||||||
chr3:47941220
|
CAA | C | 10 | a0002c0002t0002g0090a0003c0003t0003g0107a0003c0003t0003g0108others(7): Show | 10 | HG02055.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-12872_293-1287 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941220 | ||||||
chr3:47941220
|
CAAA | C | 37 | a0002c0002t0002g0089a0002c0002t0006g0026a0002c0002t0006g0040others(34): Show | 37 | HG00738.hp1 HG01074.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.293-12873_293-1287 others(7): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941220 | ||||||
chr3:47941220
|
CAAAA | C | 77 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(74): Show | 78 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.293-12874_293-1287 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941220 | ||||||
chr3:47941627
|
C | CA | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG01074.hp1 HG01169.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-13278dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941627 | ||||||
chr3:47941627
|
C | CAA | 8 | a0005c0005t0003g0114a0005c0005t0003g0115a0005c0005t0003g0117others(5): Show | 8 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-13279_293-1327 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941627 | ||||||
chr3:47941632
|
A | C | 2 | a0002c0002t0002g0069a0002c0002t0002g0231 | 2 | HG00741.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.293-13282T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941632 | ||||||
chr3:47941633
|
A | C | 21 | a0003c0003t0003g0101a0003c0003t0003g0102a0003c0003t0003g0103others(18): Show | 21 | HG01934.hp1 HG02040.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.293-13283T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941633 | ||||||
chr3:47941637
|
A | AAAAACTG others(17): Show |
1 | a0002c0002t0002g0037 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.293-13311_293-1328 others(28): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941637 | ||||||
chr3:47941701
|
T | C | 1 | a0004c0004t0021g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.293-13351A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941701 | ||||||
chr3:47941748
|
TTGCACTC others(5): Show |
T | 6 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(3): Show | 6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-13410_293-1339 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941748 | ||||||
chr3:47941762
|
G | A | 6 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(3): Show | 6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-13412C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941762 | ||||||
chr3:47941786
|
C | CA | 11 | a0001c0001t0001g0129a0001c0001t0001g0134a0001c0001t0001g0180others(8): Show | 11 | HG00639.hp2 HG02071.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.293-13437dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941786 | ||||||
chr3:47941858
|
T | G | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-13508A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941858 | ||||||
chr3:47942543
|
A | G | 15 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(12): Show | 15 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.293-14193T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47942543 | ||||||
chr3:47942696
|
G | A | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-14346C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47942696 | ||||||
chr3:47942937
|
C | T | 1 | a0004c0004t0019g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.293-14587G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47942937 | ||||||
chr3:47943263
|
G | A | 1 | a0026c0017t0002g0038 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.293-14913C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47943263 | ||||||
chr3:47943334
|
A | G | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.293-14984T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47943334 | ||||||
chr3:47943566
|
G | A | 1 | a0012c0013t0011g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.293-15216C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47943566 | ||||||
chr3:47943598
|
A | G | 1 | a0007c0008t0007g0226 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.293-15248T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47943598 | ||||||
chr3:47943871
|
C | T | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.293-15521G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47943871 | ||||||
chr3:47944215
|
C | T | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.293-15865G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47944215 | ||||||
chr3:47944242
|
G | A | 91 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(88): Show | 92 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.293-15892C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47944242 | ||||||
chr3:47944661
|
T | G | 1 | a0002c0002t0002g0045 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.293-16311A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47944661 | ||||||
chr3:47944902
|
C | T | 81 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(78): Show | 82 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.293-16552G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47944902 | ||||||
chr3:47944949
|
C | CT | 15 | a0001c0001t0001g0160a0001c0001t0001g0188a0001c0001t0001g0192others(12): Show | 16 | HG00741.hp1 HG01099.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.293-16600dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47944949 | ||||||
chr3:47944949
|
CT | C | 8 | a0001c0001t0001g0162a0001c0001t0001g0184a0001c0001t0001g0195others(5): Show | 8 | HG01891.hp1 HG02273.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-16600delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47944949 | ||||||
chr3:47945077
|
G | T | 6 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(3): Show | 6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-16727C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47945077 | ||||||
chr3:47945182
|
T | C | 1 | a0004c0004t0021g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.293-16832A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47945182 | ||||||
chr3:47945245
|
G | A | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.293-16895C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47945245 | ||||||
chr3:47945975
|
C | T | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-17625G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47945975 | ||||||
chr3:47946117
|
G | T | 1 | a0001c0001t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.293-17767C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47946117 | ||||||
chr3:47946214
|
A | T | 1 | a0001c0001t0001g0151 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.293-17864T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47946214 | ||||||
chr3:47946228
|
C | T | 8 | a0002c0002t0002g0045a0002c0002t0002g0055a0002c0002t0002g0056others(5): Show | 8 | HG02559.hp1 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-17878G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47946228 | ||||||
chr3:47946238
|
C | T | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-17888G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47946238 | ||||||
chr3:47946654
|
C | CA | 78 | a0001c0001t0001g0147a0001c0001t0001g0156a0001c0001t0001g0164others(75): Show | 79 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.293-18305dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47946654 | ||||||
chr3:47946654
|
C | CAA | 34 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0010others(31): Show | 34 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.293-18306_293-1830 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47946654 | ||||||
chr3:47946654
|
C | CAAA | 8 | a0002c0002t0002g0018a0002c0002t0002g0020a0004c0004t0005g0086others(5): Show | 8 | HG01891.hp2 HG01934.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-18307_293-1830 others(7): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47946654 | ||||||
chr3:47946654
|
CAAAAAAA others(6): Show |
C | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.293-18317_293-1830 others(17): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47946654 | ||||||
chr3:47947126
|
T | C | 1 | a0002c0002t0002g0056 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.293-18776A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47947126 | ||||||
chr3:47947190
|
T | C | 1 | a0001c0007t0001g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.293-18840A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47947190 | ||||||
chr3:47947420
|
C | T | 1 | a0002c0002t0002g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.293-19070G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47947420 | ||||||
chr3:47947704
|
G | A | 2 | a0002c0002t0002g0013a0002c0002t0002g0014 | 2 | NA19004.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.293-19354C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47947704 | ||||||
chr3:47947804
|
C | CA | 6 | a0001c0001t0001g0173a0001c0001t0001g0176a0001c0001t0024g0213others(3): Show | 6 | HG02486.hp1 HG02717.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-19455dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47947804 | ||||||
chr3:47948195
|
C | T | 1 | a0002c0002t0006g0028 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.293-19845G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47948195 | ||||||
chr3:47948225
|
C | CT | 9 | a0001c0001t0001g0214a0001c0001t0001g0216a0002c0002t0006g0026others(6): Show | 9 | HG01123.hp2 HG02602.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.293-19876dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47948225 | ||||||
chr3:47948256
|
A | G | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.293-19906T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47948256 | ||||||
chr3:47948463
|
A | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | NA18940.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.293-20113T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47948463 | ||||||
chr3:47948504
|
G | A | 1 | a0002c0020t0002g0054 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.293-20154C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47948504 | ||||||
chr3:47948951
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.293-20601C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47948951 | ||||||
chr3:47949010
|
G | C | 34 | a0002c0002t0002g0001a0002c0002t0002g0052a0002c0002t0002g0061others(31): Show | 35 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.293-20660C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949010 | ||||||
chr3:47949194
|
G | A | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.293-20844C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949194 | ||||||
chr3:47949465
|
C | CA | 20 | a0001c0001t0001g0147a0001c0001t0001g0162a0001c0001t0001g0180others(17): Show | 20 | HG00673.hp1 HG00738.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.293-21116dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949465 | ||||||
chr3:47949465
|
CA | C | 84 | a0001c0001t0001g0168a0001c0001t0001g0202a0001c0001t0024g0213others(81): Show | 85 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.293-21116delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949465 | ||||||
chr3:47949466
|
A | C | 1 | a0004c0004t0005g0086 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.293-21116T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949466 | ||||||
chr3:47949467
|
A | C | 2 | a0004c0004t0005g0084a0018c0023t0005g0053 | 2 | HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.293-21117T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949467 | ||||||
chr3:47949844
|
C | T | 9 | a0002c0002t0002g0045a0002c0002t0002g0055a0002c0002t0002g0056others(6): Show | 9 | HG02559.hp1 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.293-21494G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949844 | ||||||
chr3:47949889
|
CA | C | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.293-21540delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949889 | ||||||
chr3:47949905
|
G | C | 1 | a0027c0021t0002g0011 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.293-21555C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949905 | ||||||
chr3:47949970
|
T | C | 2 | a0007c0008t0007g0131a0007c0008t0007g0226 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.293-21620A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949970 | ||||||
chr3:47950442
|
C | T | 1 | a0005c0005t0003g0121 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.293-22092G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47950442 | ||||||
chr3:47950698
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.293-22348A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47950698 | ||||||
chr3:47951204
|
T | G | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.293-22854A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47951204 | ||||||
chr3:47951496
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.293-23146G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47951496 | ||||||
chr3:47951659
|
T | A | 1 | a0005c0005t0003g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.293-23309A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47951659 | ||||||
chr3:47951659
|
T | G | 119 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(116): Show | 120 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.293-23309A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47951659 | ||||||
chr3:47951793
|
G | A | 15 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(12): Show | 15 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.293-23443C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47951793 | ||||||
chr3:47951919
|
G | C | 1 | a0023c0027t0001g0175 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.293-23569C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47951919 | ||||||
chr3:47951943
|
T | A | 125 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.293-23593A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47951943 | ||||||
chr3:47952040
|
C | A | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.293-23690G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952040 | ||||||
chr3:47952065
|
G | A | 2 | a0004c0004t0012g0049a0004c0004t0012g0050 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.293-23715C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952065 | ||||||
chr3:47952118
|
T | C | 1 | a0005c0005t0003g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.293-23768A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952118 | ||||||
chr3:47952228
|
A | G | 173 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(170): Show | 174 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.293-23878T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952228 | ||||||
chr3:47952265
|
G | A | 1 | a0002c0002t0002g0024 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.293-23915C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952265 | ||||||
chr3:47952384
|
G | T | 4 | a0002c0002t0006g0026a0002c0002t0006g0028a0002c0002t0006g0040others(1): Show | 4 | HG01074.hp2 HG01346.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-24034C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952384 | ||||||
chr3:47952482
|
G | T | 1 | a0009c0009t0002g0048 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.293-24132C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952482 | ||||||
chr3:47952645
|
T | A | 2 | a0012c0013t0011g0222a0017c0028t0002g0224 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.293-24295A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952645 | ||||||
chr3:47952654
|
A | T | 2 | a0004c0004t0018g0083a0005c0005t0003g0115 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.293-24304T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952654 | ||||||
chr3:47952659
|
A | T | 8 | a0006c0006t0002g0062a0006c0006t0002g0074a0006c0006t0002g0075others(5): Show | 8 | HG01123.hp2 HG02602.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-24309T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952659 | ||||||
chr3:47952663
|
A | AAAAATAA others(4): Show |
1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-24314_293-2431 others(15): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952663 | ||||||
chr3:47952663
|
AAAAAATA others(5): Show |
A | 1 | a0018c0023t0005g0053 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.293-24325_293-2431 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952663 | ||||||
chr3:47952905
|
C | T | 1 | a0002c0002t0002g0036 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.293-24555G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952905 | ||||||
chr3:47952941
|
C | CA | 8 | a0001c0001t0001g0132a0002c0002t0002g0027a0002c0002t0002g0029others(5): Show | 8 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-24592dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952941 | ||||||
chr3:47953021
|
G | C | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.293-24671C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47953021 | ||||||
chr3:47953462
|
C | T | 1 | a0004c0004t0018g0083 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.292+24403G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47953462 | ||||||
chr3:47953678
|
A | C | 122 | a0001c0001t0001g0067a0002c0002t0002g0001a0002c0002t0002g0004others(119): Show | 123 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.292+24187T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47953678 | ||||||
chr3:47953734
|
G | GC | 126 | a0001c0001t0001g0067a0002c0002t0002g0001a0002c0002t0002g0004others(123): Show | 127 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.292+24130_292+2413 others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47953734 | ||||||
chr3:47954046
|
A | C | 1 | a0001c0001t0001g0200 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.292+23819T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47954046 | ||||||
chr3:47954555
|
T | A | 6 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(3): Show | 6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+23310A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47954555 | ||||||
chr3:47954925
|
T | C | 1 | a0001c0001t0010g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.292+22940A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47954925 | ||||||
chr3:47955218
|
A | G | 1 | a0026c0017t0002g0038 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.292+22647T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955218 | ||||||
chr3:47955282
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.292+22583G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955282 | ||||||
chr3:47955435
|
T | TAC | 8 | a0001c0001t0001g0129a0001c0001t0002g0150a0001c0001t0017g0135others(5): Show | 8 | HG02071.hp2 HG02135.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.292+22428_292+2242 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955435 | ||||||
chr3:47955435
|
T | TACAC | 7 | a0005c0005t0003g0114a0005c0005t0003g0115a0005c0005t0003g0117others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.292+22426_292+2242 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955435 | ||||||
chr3:47955435
|
TAC | T | 84 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0126others(81): Show | 84 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.292+22428_292+2242 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955435 | ||||||
chr3:47955435
|
TACAC | T | 42 | a0001c0001t0001g0041a0001c0001t0001g0067a0001c0001t0001g0128others(39): Show | 42 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.292+22426_292+2242 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955435 | ||||||
chr3:47955435
|
TACACAC | T | 42 | a0002c0002t0002g0001a0002c0002t0002g0027a0002c0002t0002g0029others(39): Show | 43 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.292+22424_292+2242 others(10): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955435 | ||||||
chr3:47955435
|
TACACACA others(1): Show |
T | 8 | a0002c0002t0002g0030a0002c0002t0002g0034a0002c0002t0002g0035others(5): Show | 8 | HG01981.hp2 HG03041.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+22422_292+2242 others(12): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955435 | ||||||
chr3:47955435
|
TACACACA others(3): Show |
T | 2 | a0002c0002t0002g0072a0024c0019t0002g0077 | 2 | HG04204.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.292+22420_292+2242 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955435 | ||||||
chr3:47955435
|
TACACACA others(9): Show |
T | 3 | a0001c0001t0009g0166a0001c0001t0009g0167a0002c0002t0002g0082 | 3 | HG02258.hp2 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.292+22414_292+2242 others(20): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955435 | ||||||
chr3:47955437
|
C | CGT | 2 | a0003c0003t0003g0095a0003c0003t0003g0100 | 2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.292+22427_292+2242 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955437 | ||||||
chr3:47955438
|
A | G | 14 | a0003c0003t0003g0098a0003c0003t0003g0099a0003c0003t0003g0101others(11): Show | 14 | HG02055.hp2 HG02630.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.292+22427T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955438 | ||||||
chr3:47955439
|
C | T | 14 | a0003c0003t0003g0098a0003c0003t0003g0099a0003c0003t0003g0101others(11): Show | 14 | HG02055.hp2 HG02630.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.292+22426G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955439 | ||||||
chr3:47955548
|
C | T | 6 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(3): Show | 6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+22317G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955548 | ||||||
chr3:47955942
|
G | A | 3 | a0008c0010t0008g0111a0008c0010t0008g0112a0008c0010t0008g0113 | 3 | HG00738.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.292+21923C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955942 | ||||||
chr3:47955999
|
C | T | 1 | a0005c0005t0020g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.292+21866G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955999 | ||||||
chr3:47956336
|
CAA | C | 91 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(88): Show | 92 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.292+21527_292+2152 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47956336 | ||||||
chr3:47956474
|
G | C | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.292+21391C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47956474 | ||||||
chr3:47956665
|
T | C | 1 | a0012c0013t0011g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.292+21200A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47956665 | ||||||
chr3:47956799
|
A | T | 1 | a0002c0002t0002g0036 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.292+21066T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47956799 | ||||||
chr3:47957087
|
TATA | T | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.292+20775_292+2077 others(7): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47957087 | ||||||
chr3:47957177
|
T | G | 2 | a0003c0003t0003g0106a0024c0019t0002g0077 | 2 | HG03579.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.292+20688A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47957177 | ||||||
chr3:47957288
|
C | T | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.292+20577G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47957288 | ||||||
chr3:47957418
|
G | A | 4 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0024g0213others(1): Show | 4 | HG00544.hp1 NA18982.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+20447C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47957418 | ||||||
chr3:47957476
|
A | G | 122 | a0001c0001t0001g0067a0002c0002t0002g0001a0002c0002t0002g0004others(119): Show | 123 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.292+20389T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47957476 | ||||||
chr3:47957750
|
T | G | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.292+20115A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47957750 | ||||||
chr3:47957823
|
C | T | 4 | a0007c0008t0007g0131a0007c0008t0007g0149a0007c0008t0007g0152others(1): Show | 4 | HG01891.hp1 HG02970.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+20042G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47957823 | ||||||
chr3:47957847
|
T | A | 126 | a0001c0001t0001g0067a0002c0002t0002g0001a0002c0002t0002g0004others(123): Show | 127 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.292+20018A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47957847 | ||||||
chr3:47958184
|
A | G | 126 | a0001c0001t0001g0067a0002c0002t0002g0001a0002c0002t0002g0004others(123): Show | 127 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.292+19681T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958184 | ||||||
chr3:47958293
|
T | C | 23 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0010others(20): Show | 23 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.292+19572A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958293 | ||||||
chr3:47958316
|
C | T | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.292+19549G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958316 | ||||||
chr3:47958498
|
A | G | 4 | a0001c0007t0001g0218a0001c0007t0001g0219a0001c0007t0001g0220others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+19367T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958498 | ||||||
chr3:47958629
|
G | C | 23 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0010others(20): Show | 23 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.292+19236C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958629 | ||||||
chr3:47958631
|
C | T | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.292+19234G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958631 | ||||||
chr3:47958682
|
A | AT | 12 | a0001c0001t0001g0147a0001c0001t0001g0157a0001c0001t0001g0160others(9): Show | 12 | HG00597.hp1 HG00741.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.292+19182dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958682 | ||||||
chr3:47958682
|
AT | A | 78 | a0001c0001t0001g0067a0001c0001t0001g0180a0001c0001t0001g0216others(75): Show | 79 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.292+19182delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958682 | ||||||
chr3:47958872
|
C | T | 1 | a0004c0004t0005g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.292+18993G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958872 | ||||||
chr3:47958873
|
G | A | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.292+18992C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958873 | ||||||
chr3:47959059
|
A | G | 1 | a0002c0002t0002g0035 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.292+18806T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47959059 | ||||||
chr3:47959264
|
C | T | 1 | a0012c0013t0011g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.292+18601G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47959264 | ||||||
chr3:47959301
|
T | C | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.292+18564A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47959301 | ||||||
chr3:47959319
|
G | A | 1 | a0006c0006t0002g0079 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.292+18546C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47959319 | ||||||
chr3:47959458
|
G | GA | 7 | a0001c0001t0001g0173a0001c0001t0001g0177a0002c0002t0002g0004others(4): Show | 7 | HG03579.hp2 NA18956.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.292+18406dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47959458 | ||||||
chr3:47959696
|
A | T | 1 | a0001c0001t0001g0042 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.292+18169T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47959696 | ||||||
chr3:47959758
|
C | CA | 7 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0024g0213others(4): Show | 7 | HG02965.hp1 HG03834.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.292+18106dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47959758 | ||||||
chr3:47959758
|
CA | C | 13 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(10): Show | 13 | HG01109.hp2 HG02630.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.292+18106delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47959758 | ||||||
chr3:47960458
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.292+17407A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47960458 | ||||||
chr3:47960733
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.292+17132A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47960733 | ||||||
chr3:47960735
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.292+17130C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47960735 | ||||||
chr3:47960896
|
T | G | 29 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(26): Show | 29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.292+16969A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47960896 | ||||||
chr3:47960928
|
C | G | 1 | a0003c0003t0003g0100 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.292+16937G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47960928 | ||||||
chr3:47961112
|
C | G | 1 | a0001c0001t0001g0151 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.292+16753G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47961112 | ||||||
chr3:47961150
|
T | C | 122 | a0001c0001t0001g0067a0002c0002t0002g0001a0002c0002t0002g0004others(119): Show | 123 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.292+16715A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47961150 | ||||||
chr3:47961487
|
A | G | 16 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(13): Show | 16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.292+16378T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47961487 | ||||||
chr3:47961656
|
C | A | 8 | a0002c0002t0002g0045a0002c0002t0002g0055a0002c0002t0002g0056others(5): Show | 8 | HG02559.hp1 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.292+16209G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47961656 | ||||||
chr3:47962005
|
G | T | 2 | a0002c0002t0002g0030a0002c0002t0002g0034 | 2 | NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.292+15860C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47962005 | ||||||
chr3:47962090
|
C | T | 1 | a0004c0004t0005g0086 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.292+15775G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47962090 | ||||||
chr3:47963545
|
C | A | 15 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(12): Show | 15 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.292+14320G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47963545 | ||||||
chr3:47963914
|
T | C | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.292+13951A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47963914 | ||||||
chr3:47964183
|
A | C | 121 | a0001c0001t0001g0067a0002c0002t0002g0001a0002c0002t0002g0004others(118): Show | 122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.292+13682T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47964183 | ||||||
chr3:47964773
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.292+13092A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47964773 | ||||||
chr3:47964970
|
A | C | 10 | a0005c0005t0003g0114a0005c0005t0003g0115a0005c0005t0003g0117others(7): Show | 10 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+12895T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47964970 | ||||||
chr3:47965020
|
C | T | 1 | a0001c0007t0001g0221 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.292+12845G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47965020 | ||||||
chr3:47965030
|
C | T | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.292+12835G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47965030 | ||||||
chr3:47965058
|
T | C | 1 | a0003c0003t0003g0099 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.292+12807A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47965058 | ||||||
chr3:47965118
|
G | T | 1 | a0002c0011t0002g0073 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.292+12747C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47965118 | ||||||
chr3:47965252
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.292+12613G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47965252 | ||||||
chr3:47965253
|
G | A | 1 | a0009c0009t0002g0048 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.292+12612C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47965253 | ||||||
chr3:47965973
|
C | T | 4 | a0001c0001t0001g0067a0002c0002t0002g0123a0002c0011t0002g0073others(1): Show | 4 | HG00639.hp1 HG00733.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+11892G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47965973 | ||||||
chr3:47965995
|
T | C | 2 | a0011c0014t0001g0142a0011c0014t0001g0143 | 2 | NA19007.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.292+11870A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47965995 | ||||||
chr3:47966043
|
T | A | 1 | a0004c0004t0019g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.292+11822A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966043 | ||||||
chr3:47966101
|
C | G | 1 | a0007c0008t0007g0131 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.292+11764G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966101 | ||||||
chr3:47966103
|
C | G | 6 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(3): Show | 6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+11762G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966103 | ||||||
chr3:47966150
|
T | G | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.292+11715A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966150 | ||||||
chr3:47966228
|
C | CT | 26 | a0001c0001t0001g0043a0001c0001t0001g0132a0001c0001t0001g0134others(23): Show | 26 | HG00544.hp1 HG00639.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.292+11636dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | ||||||
chr3:47966228
|
C | CTT | 27 | a0001c0001t0001g0128a0001c0001t0001g0139a0001c0001t0001g0140others(24): Show | 27 | HG00099.hp1 HG00733.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.292+11635_292+1163 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | ||||||
chr3:47966228
|
C | CTTT | 15 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0156others(12): Show | 15 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.292+11634_292+1163 others(7): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | ||||||
chr3:47966228
|
C | CTTTT | 12 | a0001c0001t0001g0042a0001c0001t0001g0136a0001c0001t0001g0159others(9): Show | 12 | HG00673.hp1 HG02451.hp1 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.292+11633_292+1163 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | ||||||
chr3:47966228
|
CT | C | 5 | a0001c0001t0001g0041a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 5 | HG01074.hp1 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+11636delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | ||||||
chr3:47966228
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.292+11627_292+1163 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | ||||||
chr3:47966228
|
CTTTTTTT others(5): Show |
C | 4 | a0001c0007t0001g0220a0003c0003t0023g0105a0004c0004t0005g0086others(1): Show | 4 | HG02071.hp2 HG02647.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+11625_292+1163 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | ||||||
chr3:47966228
|
CTTTTTTT others(6): Show |
C | 43 | a0002c0002t0002g0013a0002c0002t0002g0018a0002c0002t0002g0020others(40): Show | 43 | HG00544.hp2 HG00738.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.292+11624_292+1163 others(17): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | ||||||
chr3:47966228
|
CTTTTTTT others(7): Show |
C | 73 | a0001c0001t0001g0067a0002c0002t0002g0001a0002c0002t0002g0004others(70): Show | 74 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.292+11623_292+1163 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | ||||||
chr3:47966228
|
CTTTTTTT others(8): Show |
C | 2 | a0002c0002t0002g0052a0002c0002t0004g0003 | 2 | HG02015.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.292+11622_292+1163 others(19): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | ||||||
chr3:47966228
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0230 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.292+11621_292+1163 others(20): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | ||||||
chr3:47966228
|
CTTTTTTT others(10): Show |
C | 2 | a0015c0030t0025g0044a0020c0022t0002g0088 | 2 | HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.292+11620_292+1163 others(21): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | ||||||
chr3:47966228
|
CTTTTTTT others(12): Show |
C | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.292+11618_292+1163 others(23): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | ||||||
chr3:47966228
|
CTTTTTTT others(19): Show |
C | 1 | a0016c0029t0016g0155 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.292+11611_292+1163 others(30): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | ||||||
chr3:47966737
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.292+11128G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966737 | ||||||
chr3:47967134
|
T | G | 121 | a0001c0001t0001g0067a0002c0002t0002g0001a0002c0002t0002g0004others(118): Show | 122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.292+10731A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47967134 | ||||||
chr3:47967139
|
C | T | 2 | a0004c0004t0005g0084a0004c0004t0005g0086 | 2 | HG02083.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.292+10726G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47967139 | ||||||
chr3:47967329
|
C | T | 121 | a0001c0001t0001g0067a0002c0002t0002g0001a0002c0002t0002g0004others(118): Show | 122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.292+10536G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47967329 | ||||||
chr3:47967396
|
C | T | 126 | a0001c0001t0001g0067a0002c0002t0002g0001a0002c0002t0002g0004others(123): Show | 127 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.292+10469G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47967396 | ||||||
chr3:47967977
|
C | T | 4 | a0001c0001t0001g0208a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+9888G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47967977 | ||||||
chr3:47968146
|
A | T | 1 | a0004c0004t0018g0083 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.292+9719T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47968146 | ||||||
chr3:47968299
|
G | A | 1 | a0002c0002t0004g0007 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.292+9566C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47968299 | ||||||
chr3:47968526
|
T | C | 1 | a0021c0025t0001g0215 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.292+9339A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47968526 | ||||||
chr3:47968753
|
A | C | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.292+9112T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47968753 | ||||||
chr3:47968818
|
G | C | 16 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(13): Show | 16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.292+9047C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47968818 | ||||||
chr3:47969045
|
AC | A | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.292+8819delG | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47969045 | ||||||
chr3:47969416
|
G | A | 9 | a0002c0002t0002g0070a0002c0002t0002g0082a0002c0002t0002g0130others(6): Show | 9 | HG01123.hp2 HG02145.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+8449C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47969416 | ||||||
chr3:47969423
|
G | GA | 226 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.292+8441dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47969423 | ||||||
chr3:47969468
|
A | C | 1 | a0002c0002t0002g0035 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.292+8397T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47969468 | ||||||
chr3:47969797
|
T | C | 6 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(3): Show | 6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+8068A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47969797 | ||||||
chr3:47969846
|
C | T | 1 | a0002c0002t0002g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.292+8019G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47969846 | ||||||
chr3:47969847
|
A | G | 225 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(222): Show | 226 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(223): Show |
intron_variant | MODIFIER | c.292+8018T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47969847 | ||||||
chr3:47970118
|
A | C | 2 | a0004c0004t0012g0049a0004c0004t0012g0050 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.292+7747T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47970118 | ||||||
chr3:47970148
|
A | G | 126 | a0001c0001t0001g0067a0002c0002t0002g0001a0002c0002t0002g0004others(123): Show | 127 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.292+7717T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47970148 | ||||||
chr3:47970154
|
T | C | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.292+7711A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47970154 | ||||||
chr3:47970615
|
G | A | 4 | a0002c0002t0002g0089a0002c0002t0002g0091a0002c0002t0002g0092others(1): Show | 4 | NA18941.hp1 NA18943.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+7250C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47970615 | ||||||
chr3:47970892
|
T | C | 1 | a0001c0001t0013g0204 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.292+6973A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47970892 | ||||||
chr3:47970937
|
T | C | 2 | a0002c0002t0002g0037a0002c0002t0002g0039 | 2 | HG02135.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.292+6928A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47970937 | ||||||
chr3:47971043
|
G | C | 1 | a0017c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.292+6822C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971043 | ||||||
chr3:47971092
|
C | T | 1 | a0002c0002t0002g0118 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.292+6773G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971092 | ||||||
chr3:47971199
|
G | C | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.292+6666C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971199 | ||||||
chr3:47971307
|
C | T | 122 | a0001c0001t0001g0067a0002c0002t0002g0001a0002c0002t0002g0004others(119): Show | 123 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.292+6558G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971307 | ||||||
chr3:47971485
|
T | C | 1 | a0002c0002t0002g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.292+6380A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971485 | ||||||
chr3:47971722
|
G | A | 16 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(13): Show | 16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.292+6143C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971722 | ||||||
chr3:47971894
|
G | A | 1 | a0001c0001t0010g0205 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.292+5971C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971894 | ||||||
chr3:47971959
|
G | C | 1 | a0001c0001t0001g0146 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.292+5906C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971959 | ||||||
chr3:47971986
|
A | G | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.292+5879T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971986 | ||||||
chr3:47972172
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.292+5693C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47972172 | ||||||
chr3:47972329
|
C | T | 230 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.292+5536G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47972329 | ||||||
chr3:47972402
|
G | C | 1 | a0002c0020t0002g0054 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.292+5463C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47972402 | ||||||
chr3:47972519
|
T | C | 1 | a0002c0002t0002g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.292+5346A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47972519 | ||||||
chr3:47972715
|
C | T | 126 | a0001c0001t0001g0067a0002c0002t0002g0001a0002c0002t0002g0004others(123): Show | 127 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.292+5150G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47972715 | ||||||
chr3:47973093
|
A | C | 2 | a0004c0004t0012g0049a0004c0004t0012g0050 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.292+4772T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47973093 | ||||||
chr3:47973263
|
G | GA | 27 | a0001c0001t0001g0179a0003c0003t0003g0095a0003c0003t0003g0098others(24): Show | 27 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.292+4601dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47973263 | ||||||
chr3:47973473
|
G | A | 1 | a0018c0023t0005g0053 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.292+4392C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47973473 | ||||||
chr3:47973701
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.292+4164T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47973701 | ||||||
chr3:47973788
|
G | A | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.292+4077C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47973788 | ||||||
chr3:47974102
|
A | C | 1 | a0002c0002t0002g0012 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.292+3763T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47974102 | ||||||
chr3:47974471
|
C | G | 1 | a0001c0007t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.292+3394G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47974471 | ||||||
chr3:47974596
|
A | G | 9 | a0002c0002t0002g0052a0002c0002t0002g0089a0002c0002t0002g0090others(6): Show | 9 | HG02015.hp2 NA18747.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+3269T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47974596 | ||||||
chr3:47974682
|
T | C | 121 | a0001c0001t0001g0067a0002c0002t0002g0001a0002c0002t0002g0004others(118): Show | 122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.292+3183A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47974682 | ||||||
chr3:47974727
|
C | T | 9 | a0002c0002t0002g0052a0002c0002t0002g0089a0002c0002t0002g0090others(6): Show | 9 | HG02015.hp2 NA18747.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+3138G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47974727 | ||||||
chr3:47974910
|
G | C | 1 | a0002c0002t0002g0072 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.292+2955C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47974910 | ||||||
chr3:47975377
|
G | A | 1 | a0001c0001t0010g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.292+2488C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47975377 | ||||||
chr3:47975858
|
C | T | 2 | a0010c0015t0003g0096a0010c0015t0003g0097 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.292+2007G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47975858 | ||||||
chr3:47975892
|
C | T | 1 | a0002c0002t0002g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.292+1973G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47975892 | ||||||
chr3:47975936
|
C | T | 1 | a0002c0002t0002g0033 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.292+1929G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47975936 | ||||||
chr3:47976127
|
A | G | 126 | a0001c0001t0001g0067a0002c0002t0002g0001a0002c0002t0002g0004others(123): Show | 127 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.292+1738T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47976127 | ||||||
chr3:47976221
|
C | T | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.292+1644G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47976221 | ||||||
chr3:47976343
|
A | G | 1 | a0025c0018t0002g0023 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.292+1522T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47976343 | ||||||
chr3:47976916
|
C | T | 1 | a0002c0002t0006g0028 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.292+949G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47976916 | ||||||
chr3:47976942
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.292+923T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47976942 | ||||||
chr3:47977223
|
T | C | 1 | a0017c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.292+642A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47977223 | ||||||
chr3:47977278
|
C | T | 1 | a0002c0002t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.292+587G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47977278 | ||||||
chr3:47977381
|
T | C | 2 | a0001c0001t0009g0166a0001c0001t0009g0167 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.292+484A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47977381 | ||||||
chr3:47977691
|
T | C | 1 | a0017c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.292+174A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47977691 | ||||||
chr3:47977742
|
A | G | 104 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(101): Show | 104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.292+123T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47977742 | ||||||
chr3:47977768
|
A | G | 104 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(101): Show | 104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.292+97T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47977768 | ||||||
chr3:47978030
|
T | C | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.224-97A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47978030 | ||||||
chr3:47978264
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.224-331A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47978264 | ||||||
chr3:47978531
|
G | A | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.224-598C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47978531 | ||||||
chr3:47978647
|
A | T | 1 | a0001c0001t0001g0128 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.224-714T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47978647 | ||||||
chr3:47978673
|
T | C | 2 | a0001c0001t0024g0213a0021c0025t0001g0215 | 2 | HG00544.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.224-740A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47978673 | ||||||
chr3:47978771
|
T | C | 1 | a0017c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.224-838A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47978771 | ||||||
chr3:47979178
|
G | T | 1 | a0019c0031t0003g0109 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.224-1245C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979178 | ||||||
chr3:47979184
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0156 | 2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.224-1251C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979184 | ||||||
chr3:47979206
|
AAGTTTCT others(31): Show |
A | 1 | a0002c0002t0002g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.224-1311_224-1274d others(40): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979206 | ||||||
chr3:47979528
|
G | A | 104 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(101): Show | 104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.224-1595C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979528 | ||||||
chr3:47979599
|
G | C | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.224-1666C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979599 | ||||||
chr3:47979604
|
G | A | 2 | a0004c0004t0012g0049a0004c0004t0012g0050 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.224-1671C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979604 | ||||||
chr3:47979613
|
C | A | 2 | a0012c0013t0011g0222a0017c0028t0002g0224 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.224-1680G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979613 | ||||||
chr3:47979624
|
T | A | 1 | a0001c0001t0010g0205 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.224-1691A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979624 | ||||||
chr3:47979792
|
C | T | 40 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(37): Show | 40 | HG00544.hp1 HG00609.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.224-1859G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979792 | ||||||
chr3:47979901
|
T | C | 1 | a0001c0007t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.224-1968A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979901 | ||||||
chr3:47981083
|
A | C | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.224-3150T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47981083 | ||||||
chr3:47981217
|
T | C | 104 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(101): Show | 104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.224-3284A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47981217 | ||||||
chr3:47981478
|
A | T | 1 | a0001c0001t0001g0139 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.224-3545T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47981478 | ||||||
chr3:47981719
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG01123.hp1 HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.224-3786G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47981719 | ||||||
chr3:47981766
|
C | CA | 7 | a0001c0001t0001g0157a0002c0002t0002g0035a0002c0002t0002g0039others(4): Show | 7 | HG02135.hp1 HG02145.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.224-3834dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47981766 | ||||||
chr3:47982083
|
G | A | 1 | a0004c0004t0005g0086 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.224-4150C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47982083 | ||||||
chr3:47982271
|
C | A | 29 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(26): Show | 29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.224-4338G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47982271 | ||||||
chr3:47982434
|
G | C | 57 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(54): Show | 57 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.224-4501C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47982434 | ||||||
chr3:47982841
|
T | G | 29 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(26): Show | 29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.224-4908A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47982841 | ||||||
chr3:47982870
|
A | C | 1 | a0011c0014t0001g0142 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.224-4937T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47982870 | ||||||
chr3:47982934
|
A | G | 6 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(3): Show | 6 | NA18943.hp1 NA18946.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.224-5001T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47982934 | ||||||
chr3:47983053
|
C | G | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.224-5120G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983053 | ||||||
chr3:47983139
|
A | T | 105 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(102): Show | 105 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.224-5206T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983139 | ||||||
chr3:47983482
|
G | A | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.224-5549C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983482 | ||||||
chr3:47983490
|
G | A | 1 | a0004c0004t0021g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.224-5557C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983490 | ||||||
chr3:47983533
|
T | C | 228 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(225): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.224-5600A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983533 | ||||||
chr3:47983547
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.224-5614G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983547 | ||||||
chr3:47983639
|
C | T | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.224-5706G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983639 | ||||||
chr3:47983654
|
C | T | 1 | a0027c0021t0002g0011 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.224-5721G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983654 | ||||||
chr3:47983661
|
T | G | 1 | a0002c0002t0006g0040 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.224-5728A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983661 | ||||||
chr3:47983822
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.224-5889A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983822 | ||||||
chr3:47984632
|
G | C | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.224-6699C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47984632 | ||||||
chr3:47984669
|
T | TA | 10 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(7): Show | 10 | HG01934.hp1 HG02040.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.224-6737dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47984669 | ||||||
chr3:47984682
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.224-6749T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47984682 | ||||||
chr3:47984684
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.224-6751T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47984684 | ||||||
chr3:47984796
|
C | A | 1 | a0004c0004t0018g0083 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.224-6863G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47984796 | ||||||
chr3:47985117
|
C | T | 222 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.224-7184G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47985117 | ||||||
chr3:47985125
|
C | G | 2 | a0004c0004t0019g0060a0004c0004t0021g0080 | 2 | HG01934.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.224-7192G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47985125 | ||||||
chr3:47985383
|
G | T | 1 | a0001c0001t0001g0210 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.224-7450C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47985383 | ||||||
chr3:47985475
|
T | A | 1 | a0002c0002t0002g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.224-7542A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47985475 | ||||||
chr3:47985915
|
T | C | 1 | a0004c0004t0005g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.224-7982A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47985915 | ||||||
chr3:47986159
|
G | A | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.224-8226C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986159 | ||||||
chr3:47986342
|
G | T | 148 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(145): Show | 148 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.224-8409C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986342 | ||||||
chr3:47986353
|
T | A | 1 | a0001c0001t0001g0172 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.224-8420A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986353 | ||||||
chr3:47986361
|
G | T | 104 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(101): Show | 104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.224-8428C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986361 | ||||||
chr3:47986474
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG01109.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.224-8541C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986474 | ||||||
chr3:47986481
|
C | T | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.224-8548G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986481 | ||||||
chr3:47986486
|
G | A | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.224-8553C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986486 | ||||||
chr3:47986654
|
T | A | 104 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(101): Show | 104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.224-8721A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986654 | ||||||
chr3:47986696
|
G | A | 1 | a0001c0007t0001g0221 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.224-8763C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986696 | ||||||
chr3:47986698
|
TA | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG01123.hp1 HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.224-8766delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986698 | ||||||
chr3:47986878
|
C | T | 3 | a0002c0002t0002g0021a0002c0002t0002g0024a0025c0018t0002g0023 | 3 | HG01496.hp2 HG01943.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.224-8945G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986878 | ||||||
chr3:47987146
|
T | C | 7 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.224-9213A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47987146 | ||||||
chr3:47987214
|
T | C | 1 | a0002c0002t0002g0039 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.224-9281A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47987214 | ||||||
chr3:47987287
|
G | C | 2 | a0001c0001t0001g0206a0001c0001t0001g0217 | 2 | NA18983.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.224-9354C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47987287 | ||||||
chr3:47987307
|
G | A | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.224-9374C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47987307 | ||||||
chr3:47987337
|
A | G | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.224-9404T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47987337 | ||||||
chr3:47987421
|
G | A | 1 | a0004c0004t0005g0085 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.224-9488C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47987421 | ||||||
chr3:47987628
|
A | C | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.224-9695T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47987628 | ||||||
chr3:47987916
|
C | G | 1 | a0013c0012t0002g0078 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.224-9983G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47987916 | ||||||
chr3:47988257
|
ATT | A | 104 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(101): Show | 104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.224-10326_224-1032 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47988257 | ||||||
chr3:47988282
|
T | A | 1 | a0004c0004t0005g0085 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.224-10349A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47988282 | ||||||
chr3:47988456
|
T | C | 1 | a0002c0002t0002g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.223+10182A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47988456 | ||||||
chr3:47988512
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0217 | 2 | NA18983.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.223+10126C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47988512 | ||||||
chr3:47988660
|
A | G | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.223+9978T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47988660 | ||||||
chr3:47988861
|
T | G | 148 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(145): Show | 148 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.223+9777A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47988861 | ||||||
chr3:47988970
|
C | T | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.223+9668G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47988970 | ||||||
chr3:47989046
|
G | A | 2 | a0012c0013t0011g0222a0017c0028t0002g0224 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.223+9592C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47989046 | ||||||
chr3:47989409
|
A | T | 1 | a0002c0002t0002g0018 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.223+9229T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47989409 | ||||||
chr3:47989590
|
T | C | 1 | a0004c0004t0019g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.223+9048A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47989590 | ||||||
chr3:47989676
|
C | T | 2 | a0008c0010t0008g0111a0008c0010t0008g0112 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.223+8962G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47989676 | ||||||
chr3:47989677
|
G | GT | 2 | a0001c0001t0001g0127a0001c0001t0001g0136 | 2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.223+8960dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47989677 | ||||||
chr3:47989806
|
A | G | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.223+8832T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47989806 | ||||||
chr3:47990202
|
A | T | 4 | a0001c0001t0001g0134a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | HG00639.hp2 HG00733.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+8436T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47990202 | ||||||
chr3:47990309
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.223+8329T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47990309 | ||||||
chr3:47990561
|
G | A | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.223+8077C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47990561 | ||||||
chr3:47990677
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.223+7961T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47990677 | ||||||
chr3:47990723
|
G | A | 2 | a0002c0002t0004g0015a0002c0002t0004g0016 | 2 | NA19005.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.223+7915C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47990723 | ||||||
chr3:47990842
|
A | AT | 226 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.223+7795dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47990842 | ||||||
chr3:47990867
|
G | T | 104 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(101): Show | 104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.223+7771C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47990867 | ||||||
chr3:47991451
|
G | A | 4 | a0002c0002t0002g0091a0012c0013t0011g0002a0012c0013t0011g0222others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+7187C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47991451 | ||||||
chr3:47991459
|
C | T | 1 | a0002c0002t0002g0063 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.223+7179G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47991459 | ||||||
chr3:47991686
|
C | T | 2 | a0004c0004t0019g0060a0004c0004t0021g0080 | 2 | HG01934.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.223+6952G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47991686 | ||||||
chr3:47991713
|
G | A | 1 | a0004c0004t0019g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.223+6925C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47991713 | ||||||
chr3:47992036
|
G | A | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.223+6602C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47992036 | ||||||
chr3:47992300
|
G | A | 2 | a0004c0004t0019g0060a0004c0004t0021g0080 | 2 | HG01934.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.223+6338C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47992300 | ||||||
chr3:47992563
|
G | T | 1 | a0002c0002t0002g0012 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.223+6075C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47992563 | ||||||
chr3:47992584
|
C | T | 2 | a0010c0015t0003g0096a0010c0015t0003g0097 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.223+6054G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47992584 | ||||||
chr3:47992685
|
T | C | 31 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0010others(28): Show | 31 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.223+5953A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47992685 | ||||||
chr3:47992903
|
T | TA | 22 | a0001c0001t0001g0229a0002c0002t0004g0017a0002c0002t0022g0064others(19): Show | 22 | HG01109.hp2 HG02040.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.223+5734dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47992903 | ||||||
chr3:47992903
|
TA | T | 6 | a0001c0024t0001g0133a0002c0002t0002g0004a0002c0002t0002g0005others(3): Show | 6 | HG00280.hp1 HG01074.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+5734delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47992903 | ||||||
chr3:47993195
|
G | A | 1 | a0003c0003t0023g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.223+5443C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47993195 | ||||||
chr3:47993927
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.223+4711G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47993927 | ||||||
chr3:47993961
|
A | G | 1 | a0004c0004t0005g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.223+4677T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47993961 | ||||||
chr3:47994068
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.223+4570A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47994068 | ||||||
chr3:47994948
|
C | CA | 23 | a0001c0001t0001g0129a0001c0001t0001g0158a0001c0001t0001g0162others(20): Show | 23 | HG01109.hp2 HG01516.hp2 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.223+3689dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47994948 | ||||||
chr3:47995250
|
C | CT | 13 | a0002c0002t0002g0030a0002c0002t0002g0036a0002c0002t0002g0039others(10): Show | 13 | HG01891.hp2 HG02135.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.223+3387dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995250 | ||||||
chr3:47995250
|
CT | C | 103 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.223+3387delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995250 | ||||||
chr3:47995399
|
C | T | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.223+3239G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995399 | ||||||
chr3:47995531
|
G | A | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.223+3107C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995531 | ||||||
chr3:47995588
|
G | A | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.223+3050C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995588 | ||||||
chr3:47995621
|
C | G | 2 | a0011c0014t0001g0142a0011c0014t0001g0143 | 2 | NA19007.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.223+3017G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995621 | ||||||
chr3:47995697
|
C | T | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.223+2941G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995697 | ||||||
chr3:47995722
|
A | G | 1 | a0008c0010t0008g0112 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.223+2916T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995722 | ||||||
chr3:47995851
|
T | C | 1 | a0002c0002t0002g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.223+2787A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995851 | ||||||
chr3:47996042
|
T | C | 1 | a0002c0002t0002g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.223+2596A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996042 | ||||||
chr3:47996124
|
T | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | NA18963.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.223+2514A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996124 | ||||||
chr3:47996599
|
G | C | 1 | a0001c0007t0001g0221 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.223+2039C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996599 | ||||||
chr3:47996737
|
G | GAC | 5 | a0001c0001t0001g0227a0002c0002t0002g0055a0002c0011t0002g0073others(2): Show | 5 | HG00733.hp1 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+1899_223+1900d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | ||||||
chr3:47996737
|
G | GACAC | 39 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0010others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.223+1897_223+1900d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | ||||||
chr3:47996737
|
G | GACACAC | 9 | a0004c0004t0005g0084a0004c0004t0005g0085a0004c0004t0005g0086others(6): Show | 9 | HG00597.hp2 HG01934.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.223+1895_223+1900d others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | ||||||
chr3:47996737
|
G | GACACACA others(1): Show |
18 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(15): Show | 18 | HG01109.hp2 HG01891.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.223+1893_223+1900d others(10): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | ||||||
chr3:47996737
|
G | GACACACA others(3): Show |
9 | a0004c0004t0012g0049a0004c0004t0019g0060a0005c0005t0003g0114others(6): Show | 9 | HG02258.hp1 HG02486.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.223+1891_223+1900d others(12): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | ||||||
chr3:47996737
|
G | GACACACA others(5): Show |
2 | a0003c0003t0003g0107a0005c0005t0003g0121 | 2 | HG02055.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.223+1889_223+1900d others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | ||||||
chr3:47996737
|
G | GACACACA others(9): Show |
2 | a0005c0005t0003g0115a0005c0005t0003g0117 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.223+1885_223+1900d others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | ||||||
chr3:47996737
|
G | GACACACA others(11): Show |
1 | a0008c0010t0008g0112 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.223+1883_223+1900d others(20): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | ||||||
chr3:47996737
|
G | GACACACA others(13): Show |
1 | a0008c0010t0008g0113 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.223+1881_223+1900d others(22): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | ||||||
chr3:47996737
|
GAC | G | 10 | a0001c0001t0001g0126a0001c0001t0001g0161a0001c0001t0001g0162others(7): Show | 10 | HG00609.hp1 HG00609.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.223+1899_223+1900d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | ||||||
chr3:47996737
|
GACAC | G | 94 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.223+1897_223+1900d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | ||||||
chr3:47997224
|
C | T | 104 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(101): Show | 104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.223+1414G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997224 | ||||||
chr3:47997276
|
CAAG | C | 2 | a0002c0002t0002g0037a0002c0002t0002g0039 | 2 | HG02135.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.223+1359_223+1361d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997276 | ||||||
chr3:47997326
|
T | TAAAAAA | 5 | a0002c0002t0002g0063a0002c0002t0006g0040a0002c0002t0022g0064others(2): Show | 5 | HG00280.hp2 HG01074.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+1306_223+1311d others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(2): Show |
10 | a0005c0005t0003g0114a0005c0005t0003g0115a0005c0005t0003g0117others(7): Show | 10 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.223+1303_223+1311d others(11): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(3): Show |
13 | a0003c0003t0003g0095a0003c0003t0003g0100a0003c0003t0003g0101others(10): Show | 13 | HG01109.hp2 HG02717.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.223+1302_223+1311d others(12): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(4): Show |
8 | a0002c0002t0002g0082a0002c0002t0002g0091a0003c0003t0003g0107others(5): Show | 8 | HG01891.hp2 HG01934.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+1301_223+1311d others(13): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(5): Show |
2 | a0004c0004t0012g0049a0015c0030t0025g0044 | 2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.223+1300_223+1311d others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(6): Show |
6 | a0002c0002t0014g0065a0004c0004t0005g0084a0004c0004t0005g0085others(3): Show | 6 | HG02071.hp2 HG02083.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+1299_223+1311d others(15): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(7): Show |
1 | a0004c0004t0005g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.223+1298_223+1311d others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(8): Show |
2 | a0002c0002t0002g0094a0004c0004t0005g0086 | 2 | NA19000.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.223+1297_223+1311d others(17): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(9): Show |
1 | a0002c0002t0002g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.223+1296_223+1311d others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(10): Show |
2 | a0002c0002t0002g0092a0002c0002t0002g0093 | 2 | NA18970.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.223+1295_223+1311d others(19): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(12): Show |
1 | a0002c0002t0002g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.223+1293_223+1311d others(21): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(14): Show |
6 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0032others(3): Show | 6 | HG00544.hp2 HG02145.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+1311_223+1312i others(23): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(15): Show |
14 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0025others(11): Show | 14 | HG00099.hp2 HG02015.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.223+1311_223+1312i others(24): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(16): Show |
11 | a0002c0002t0002g0001a0002c0002t0002g0010a0002c0002t0002g0020others(8): Show | 12 | HG00597.hp2 HG01257.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.223+1311_223+1312i others(25): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(17): Show |
7 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(4): Show | 7 | HG00673.hp2 HG00735.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.223+1311_223+1312i others(26): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(18): Show |
7 | a0002c0002t0002g0061a0002c0002t0006g0026a0002c0002t0006g0028others(4): Show | 7 | HG01123.hp2 HG01169.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.223+1311_223+1312i others(27): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(19): Show |
1 | a0002c0011t0002g0087 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.223+1311_223+1312i others(28): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(20): Show |
3 | a0001c0001t0001g0067a0002c0002t0002g0045a0024c0019t0002g0077 | 3 | HG01516.hp1 HG03540.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.223+1311_223+1312i others(29): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(21): Show |
4 | a0002c0002t0002g0068a0002c0002t0002g0069a0002c0002t0002g0070others(1): Show | 4 | HG01099.hp1 HG02615.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+1311_223+1312i others(30): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(22): Show |
1 | a0002c0002t0004g0016 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.223+1311_223+1312i others(31): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(23): Show |
3 | a0002c0002t0002g0051a0006c0006t0002g0062a0013c0012t0002g0071 | 3 | HG02300.hp1 HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.223+1311_223+1312i others(32): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(25): Show |
3 | a0002c0002t0002g0055a0002c0002t0002g0072a0002c0002t0002g0090 | 3 | HG03098.hp1 NA18998.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.223+1311_223+1312i others(34): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(26): Show |
1 | a0002c0002t0002g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.223+1311_223+1312i others(35): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(27): Show |
1 | a0002c0002t0002g0089 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.223+1311_223+1312i others(36): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(28): Show |
2 | a0002c0002t0002g0056a0002c0011t0002g0073 | 2 | HG00733.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.223+1311_223+1312i others(37): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(29): Show |
1 | a0002c0002t0002g0231 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.223+1311_223+1312i others(38): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(31): Show |
1 | a0002c0002t0002g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.223+1311_223+1312i others(40): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(32): Show |
1 | a0013c0012t0002g0078 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.223+1311_223+1312i others(41): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997326
|
T | TAAAAAAA others(34): Show |
3 | a0002c0002t0002g0125a0002c0020t0002g0054a0014c0032t0002g0059 | 3 | HG02723.hp2 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.223+1311_223+1312i others(43): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | ||||||
chr3:47997397
|
T | C | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.223+1241A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997397 | ||||||
chr3:47997707
|
C | CAAAG | 11 | a0002c0002t0002g0090a0004c0004t0005g0084a0004c0004t0005g0085others(8): Show | 11 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.223+927_223+930dup others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997707 | ||||||
chr3:47997707
|
C | CAAAGAAA others(5): Show |
3 | a0004c0004t0012g0049a0004c0004t0012g0050a0004c0004t0018g0083 | 3 | HG03041.hp2 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.223+919_223+930dup others(12): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997707 | ||||||
chr3:47997809
|
T | G | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.223+829A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997809 | ||||||
chr3:47998418
|
A | G | 4 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG01255.hp1 HG02015.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+220T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47998418 | ||||||
chr3:47998540
|
A | G | 1 | a0004c0004t0019g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.223+98T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47998540 | ||||||
chr3:47999238
|
T | C | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-19-359A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 47999238 | ||||||
chr3:47999772
|
C | A | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-19-893G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 47999772 | ||||||
chr3:47999845
|
TA | T | 122 | a0001c0001t0001g0067a0001c0001t0001g0229a0002c0002t0002g0001others(119): Show | 123 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.-19-967delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 47999845 | ||||||
chr3:47999845
|
TAA | T | 104 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(101): Show | 104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-19-968_-19-967del others(2): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 47999845 | ||||||
chr3:47999981
|
G | A | 16 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(13): Show | 16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19-1102C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 47999981 | ||||||
chr3:48000025
|
G | T | 1 | a0002c0002t0002g0039 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-19-1146C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000025 | ||||||
chr3:48000130
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19-1251C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000130 | ||||||
chr3:48000221
|
C | CA | 45 | a0001c0001t0001g0132a0001c0001t0001g0227a0002c0002t0002g0018others(42): Show | 45 | HG00544.hp2 HG00738.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.-19-1343dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000221 | ||||||
chr3:48000221
|
C | CAA | 51 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0161others(48): Show | 51 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.-19-1344_-19-1343d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000221 | ||||||
chr3:48000221
|
C | CAAA | 11 | a0001c0001t0001g0042a0001c0001t0001g0169a0001c0001t0001g0170others(8): Show | 11 | HG01074.hp1 HG02280.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19-1345_-19-1343d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000221 | ||||||
chr3:48000221
|
CAAAAAAA others(2): Show |
C | 44 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(41): Show | 44 | HG00544.hp1 HG00639.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.-19-1351_-19-1343d others(11): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000221 | ||||||
chr3:48000257
|
G | T | 1 | a0002c0002t0006g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-19-1378C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000257 | ||||||
chr3:48000455
|
G | T | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-19-1576C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000455 | ||||||
chr3:48000702
|
T | C | 13 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19-1823A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000702 | ||||||
chr3:48001018
|
T | C | 1 | a0001c0001t0010g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-19-2139A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48001018 | ||||||
chr3:48001232
|
G | A | 1 | a0006c0006t0002g0079 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-19-2353C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48001232 | ||||||
chr3:48001350
|
T | C | 1 | a0003c0003t0003g0108 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-19-2471A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48001350 | ||||||
chr3:48001568
|
T | C | 148 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(145): Show | 148 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.-19-2689A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48001568 | ||||||
chr3:48001917
|
C | A | 1 | a0001c0001t0001g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-19-3038G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48001917 | ||||||
chr3:48002206
|
A | C | 1 | a0001c0001t0001g0162 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-19-3327T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002206 | ||||||
chr3:48002241
|
C | CA | 3 | a0001c0001t0001g0206a0001c0001t0001g0229a0018c0023t0005g0053 | 3 | HG02071.hp2 HG02738.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-19-3363dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002241 | ||||||
chr3:48002246
|
AG | A | 5 | a0001c0001t0001g0137a0004c0004t0012g0049a0004c0004t0012g0050others(2): Show | 5 | HG01934.hp1 HG02015.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-3368delC | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002246 | ||||||
chr3:48002247
|
G | A | 143 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(140): Show | 143 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.-19-3368C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002247 | ||||||
chr3:48002258
|
G | GA | 11 | a0005c0005t0003g0114a0005c0005t0003g0115a0005c0005t0003g0117others(8): Show | 11 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19-3380dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002258 | ||||||
chr3:48002606
|
T | C | 1 | a0002c0011t0002g0087 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-19-3727A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002606 | ||||||
chr3:48002755
|
C | T | 1 | a0017c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-19-3876G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002755 | ||||||
chr3:48002769
|
T | TACTC | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.-19-3891_-19-3890i others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002769 | ||||||
chr3:48002912
|
A | T | 2 | a0004c0004t0019g0060a0004c0004t0021g0080 | 2 | HG01934.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-19-4033T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002912 | ||||||
chr3:48002954
|
A | AAAAT | 75 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.-19-4079_-19-4076d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002954 | ||||||
chr3:48002954
|
A | AAAATAAA others(1): Show |
42 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0129others(39): Show | 42 | HG00609.hp1 HG00609.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-19-4083_-19-4076d others(10): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002954 | ||||||
chr3:48002954
|
A | AAAATAAA others(5): Show |
6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0216others(3): Show | 6 | HG02015.hp1 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-4087_-19-4076d others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002954 | ||||||
chr3:48002954
|
A | AAAATAAA others(9): Show |
1 | a0021c0025t0001g0215 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-19-4091_-19-4076d others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002954 | ||||||
chr3:48002954
|
A | AAAATAAA others(13): Show |
2 | a0001c0001t0001g0214a0001c0001t0024g0213 | 2 | NA19006.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.-19-4095_-19-4076d others(22): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002954 | ||||||
chr3:48002954
|
AAAAT | A | 13 | a0001c0001t0001g0162a0001c0001t0001g0163a0005c0005t0003g0114others(10): Show | 13 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-4079_-19-4076d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002954 | ||||||
chr3:48002954
|
AAAATAAA others(1): Show |
A | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0002c0002t0002g0231 | 3 | HG00738.hp2 HG00741.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-19-4083_-19-4076d others(10): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002954 | ||||||
chr3:48002977
|
A | ATAAAT | 3 | a0001c0001t0001g0127a0001c0001t0001g0136a0001c0001t0017g0135 | 3 | HG03139.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-19-4103_-19-4099d others(7): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002977 | ||||||
chr3:48002991
|
A | AAATAAAT others(5): Show |
1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-19-4113_-19-4112i others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002991 | ||||||
chr3:48002991
|
A | AAATTAAT others(5): Show |
2 | a0012c0013t0011g0222a0017c0028t0002g0224 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-19-4113_-19-4112i others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002991 | ||||||
chr3:48003453
|
C | CA | 31 | a0002c0002t0002g0082a0002c0002t0002g0123a0002c0002t0002g0130others(28): Show | 31 | HG00639.hp1 HG01123.hp2 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.-19-4575dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003453 | ||||||
chr3:48003453
|
CA | C | 5 | a0002c0020t0002g0054a0009c0009t0002g0046a0009c0009t0002g0047others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-4575delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003453 | ||||||
chr3:48003453
|
CAA | C | 5 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(2): Show | 5 | HG01257.hp2 HG01934.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-4576_-19-4575d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003453 | ||||||
chr3:48003453
|
CAAA | C | 94 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-19-4577_-19-4575d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003453 | ||||||
chr3:48003453
|
CAAAA | C | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG01074.hp1 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-4578_-19-4575d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003453 | ||||||
chr3:48003573
|
CT | C | 27 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0010others(24): Show | 27 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.-19-4695delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003573 | ||||||
chr3:48003647
|
C | A | 105 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(102): Show | 105 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-19-4768G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003647 | ||||||
chr3:48003805
|
A | G | 1 | a0020c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-19-4926T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003805 | ||||||
chr3:48003962
|
C | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-19-5083G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003962 | ||||||
chr3:48004066
|
T | C | 222 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-19-5187A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48004066 | ||||||
chr3:48004402
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-19-5523T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48004402 | ||||||
chr3:48004541
|
G | A | 1 | a0004c0004t0005g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-19-5662C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48004541 | ||||||
chr3:48004543
|
T | C | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-19-5664A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48004543 | ||||||
chr3:48004576
|
A | G | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19-5697T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48004576 | ||||||
chr3:48004820
|
C | T | 1 | a0002c0002t0002g0027 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-19-5941G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48004820 | ||||||
chr3:48004854
|
A | G | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19-5975T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48004854 | ||||||
chr3:48005114
|
T | C | 222 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-19-6235A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005114 | ||||||
chr3:48005186
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-19-6307G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005186 | ||||||
chr3:48005218
|
G | C | 16 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(13): Show | 16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19-6339C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005218 | ||||||
chr3:48005254
|
G | A | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19-6375C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005254 | ||||||
chr3:48005255
|
G | A | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19-6376C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005255 | ||||||
chr3:48005256
|
C | G | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19-6377G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005256 | ||||||
chr3:48005258
|
G | C | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19-6379C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005258 | ||||||
chr3:48005261
|
T | A | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19-6382A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005261 | ||||||
chr3:48005305
|
G | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-19-6426C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005305 | ||||||
chr3:48005335
|
T | TG | 138 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.-19-6457dupC | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005335 | ||||||
chr3:48005410
|
A | C | 104 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(101): Show | 104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-19-6531T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005410 | ||||||
chr3:48005553
|
A | G | 29 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(26): Show | 29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.-19-6674T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005553 | ||||||
chr3:48005698
|
A | G | 2 | a0012c0013t0011g0222a0017c0028t0002g0224 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-19-6819T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005698 | ||||||
chr3:48006151
|
T | C | 1 | a0002c0002t0002g0025 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-19-7272A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48006151 | ||||||
chr3:48006231
|
C | CCA | 60 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.-19-7353_-19-7352i others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48006231 | ||||||
chr3:48006384
|
C | T | 108 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(105): Show | 108 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.-19-7505G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48006384 | ||||||
chr3:48006498
|
T | C | 1 | a0002c0002t0002g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-19-7619A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48006498 | ||||||
chr3:48007037
|
C | T | 3 | a0008c0010t0008g0111a0008c0010t0008g0112a0008c0010t0008g0113 | 3 | HG00738.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-19-8158G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48007037 | ||||||
chr3:48007676
|
C | CT | 30 | a0002c0002t0006g0026a0003c0003t0003g0095a0003c0003t0003g0098others(27): Show | 30 | HG00738.hp1 HG01109.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.-20+8657dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48007676 | ||||||
chr3:48007676
|
CT | C | 107 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(104): Show | 107 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.-20+8657delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48007676 | ||||||
chr3:48007840
|
T | A | 1 | a0002c0002t0002g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-20+8494A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48007840 | ||||||
chr3:48007940
|
A | G | 1 | a0002c0002t0002g0045 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-20+8394T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48007940 | ||||||
chr3:48008006
|
G | A | 9 | a0002c0002t0002g0052a0002c0002t0002g0089a0002c0002t0002g0090others(6): Show | 9 | HG02015.hp2 NA18747.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8328C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48008006 | ||||||
chr3:48008612
|
C | A | 4 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0024g0213others(1): Show | 4 | HG00544.hp1 NA18982.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+7722G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48008612 | ||||||
chr3:48008701
|
G | A | 1 | a0015c0030t0025g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-20+7633C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48008701 | ||||||
chr3:48008703
|
G | A | 1 | a0003c0003t0003g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-20+7631C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48008703 | ||||||
chr3:48008740
|
C | T | 2 | a0001c0001t0001g0132a0007c0008t0007g0131 | 2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-20+7594G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48008740 | ||||||
chr3:48008767
|
C | A | 1 | a0001c0001t0001g0217 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-20+7567G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48008767 | ||||||
chr3:48008950
|
T | C | 1 | a0002c0002t0002g0094 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-20+7384A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48008950 | ||||||
chr3:48009066
|
A | G | 16 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(13): Show | 16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-20+7268T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48009066 | ||||||
chr3:48009440
|
G | A | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-20+6894C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48009440 | ||||||
chr3:48009566
|
A | C | 1 | a0002c0002t0002g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-20+6768T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48009566 | ||||||
chr3:48010238
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-20+6096T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48010238 | ||||||
chr3:48010321
|
A | G | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-20+6013T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48010321 | ||||||
chr3:48010495
|
T | A | 26 | a0003c0003t0003g0095a0003c0003t0003g0098a0003c0003t0003g0099others(23): Show | 26 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.-20+5839A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48010495 | ||||||
chr3:48010843
|
C | T | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-20+5491G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48010843 | ||||||
chr3:48010902
|
G | A | 2 | a0001c0007t0001g0218a0001c0007t0001g0219 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-20+5432C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48010902 | ||||||
chr3:48011344
|
C | T | 1 | a0002c0002t0002g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-20+4990G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48011344 | ||||||
chr3:48011529
|
C | T | 1 | a0002c0002t0004g0003 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-20+4805G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48011529 | ||||||
chr3:48011575
|
A | G | 1 | a0005c0005t0003g0119 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-20+4759T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48011575 | ||||||
chr3:48011644
|
T | C | 2 | a0001c0007t0001g0220a0001c0007t0001g0221 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-20+4690A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48011644 | ||||||
chr3:48012057
|
C | T | 2 | a0004c0004t0012g0049a0004c0004t0012g0050 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-20+4277G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48012057 | ||||||
chr3:48012214
|
A | G | 3 | a0009c0009t0002g0046a0009c0009t0002g0047a0009c0009t0002g0048 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-20+4120T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48012214 | ||||||
chr3:48012429
|
T | G | 23 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0010others(20): Show | 23 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.-20+3905A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48012429 | ||||||
chr3:48012966
|
CTGT | C | 104 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(101): Show | 104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-20+3365_-20+3367d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48012966 | ||||||
chr3:48012981
|
T | C | 5 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0024others(2): Show | 5 | HG00099.hp2 HG00673.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+3353A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48012981 | ||||||
chr3:48013015
|
G | A | 1 | a0002c0002t0002g0118 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-20+3319C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48013015 | ||||||
chr3:48013054
|
A | G | 1 | a0002c0002t0002g0045 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-20+3280T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48013054 | ||||||
chr3:48013063
|
A | G | 106 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(103): Show | 106 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.-20+3271T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48013063 | ||||||
chr3:48013709
|
T | TA | 106 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(103): Show | 106 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.-20+2624dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48013709 | ||||||
chr3:48013765
|
C | G | 229 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-20+2569G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48013765 | ||||||
chr3:48013776
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-20+2558G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48013776 | ||||||
chr3:48013829
|
A | G | 23 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0010others(20): Show | 23 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.-20+2505T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48013829 | ||||||
chr3:48014621
|
T | C | 1 | a0002c0002t0002g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-20+1713A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48014621 | ||||||
chr3:48014812
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-20+1522T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48014812 | ||||||
chr3:48014911
|
C | T | 229 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-20+1423G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48014911 | ||||||
chr3:48014919
|
T | C | 105 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(102): Show | 105 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-20+1415A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48014919 | ||||||
chr3:48014966
|
G | A | 3 | a0012c0013t0011g0002a0012c0013t0011g0222a0017c0028t0002g0224 | 3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-20+1368C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48014966 | ||||||
chr3:48015149
|
C | A | 1 | a0004c0004t0005g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-20+1185G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48015149 | ||||||
chr3:48015196
|
T | A | 1 | a0017c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-20+1138A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48015196 | ||||||
chr3:48015321
|
T | G | 4 | a0001c0001t0001g0225a0001c0001t0001g0227a0001c0001t0001g0228others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+1013A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48015321 | ||||||
chr3:48015354
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-20+980C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48015354 | ||||||
chr3:48015413
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-20+921A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48015413 | ||||||
chr3:48015657
|
A | C | 41 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(38): Show | 41 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.-20+677T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48015657 | ||||||
chr3:48015957
|
C | A | 1 | a0001c0001t0001g0230 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-20+377G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48015957 | ||||||
chr3:48016113
|
G | A | 1 | a0002c0002t0002g0231 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-20+221C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48016113 | ||||||
chr3:48016220
|
C | T | 1 | a0012c0013t0011g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-20+114G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48016220 |