geneid | 4214 |
---|---|
ensemblid | ENSG00000095015.6 |
hgncid | 6848 |
symbol | MAP3K1 |
name | mitogen-activated protein kinase kinase kinase 1 |
refseq_nuc | NM_005921.2 |
refseq_prot | NP_005912.1 |
ensembl_nuc | ENST00000399503.4 |
ensembl_prot | ENSP00000382423.3 |
mane_status | MANE Select |
chr | chr5 |
start | 56815549 |
end | 56896152 |
strand | + |
ver | v1.2 |
region | chr5:56815549-56896152 |
region5000 | chr5:56810549-56901152 |
regionname0 | MAP3K1_chr5_56815549_56896152 |
regionname5000 | MAP3K1_chr5_56810549_56901152 |
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 | 0/0 | 1511 | 149 | 42 | 30 | 51 | 8 | 18 | 42 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002 | 1/0 | 1512 | 133 | 20 | 25 | 73 | 2 | 12 | 54 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0003 | 0/0 | 1511 | 86 | 18 | 9 | 44 | 2 | 13 | 33 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0004 | 0/0 | 1511 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0005 | 0/0 | 1511 | 4 | 0 | 3 | 1 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0006 | 0/1 | 1511 | 2 | 0 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0007 | 0/0 | 1512 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0008 | 0/0 | 1512 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0009 | 0/0 | 1511 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0010 | 0/0 | 1512 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0011 | 0/0 | 1511 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0012 | 0/0 | 1512 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 4536 | 93 | 26 | 26 | 21 | 6 | 14 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0002 | 0/0 | 4536 | 82 | 15 | 8 | 44 | 2 | 13 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0003 | 1/0 | 4539 | 80 | 16 | 10 | 47 | 1 | 5 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0004 | 0/0 | 4539 | 45 | 3 | 8 | 26 | 1 | 7 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0005 | 0/0 | 4536 | 26 | 5 | 0 | 18 | 0 | 3 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0006 | 0/0 | 4536 | 21 | 3 | 3 | 12 | 2 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0007 | 0/0 | 4539 | 8 | 1 | 7 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0008 | 0/0 | 4536 | 5 | 5 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0009 | 0/0 | 4536 | 4 | 3 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0010 | 0/0 | 4536 | 4 | 0 | 3 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0011 | 0/0 | 4536 | 4 | 3 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0012 | 0/0 | 4536 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0013 | 0/1 | 4536 | 2 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0014 | 0/0 | 4539 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0015 | 0/0 | 4536 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0016 | 0/0 | 4536 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0017 | 0/0 | 4536 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0018 | 0/0 | 4539 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0019 | 0/0 | 4539 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
c0020 | 0/0 | 4539 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2498 | 74 | 18 | 15 | 34 | 2 | 5 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0002 | 0/1 | 2497 | 72 | 11 | 26 | 13 | 6 | 15 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0003 | 0/0 | 2496 | 53 | 0 | 6 | 35 | 2 | 10 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0004 | 0/0 | 2500 | 38 | 4 | 5 | 24 | 2 | 3 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0005 | 0/0 | 2499 | 30 | 1 | 4 | 18 | 0 | 7 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0006 | 1/0 | 2498 | 20 | 0 | 0 | 19 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0007 | 0/0 | 2497 | 16 | 9 | 1 | 6 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0008 | 0/0 | 2498 | 12 | 6 | 0 | 6 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0009 | 0/0 | 2500 | 9 | 9 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0010 | 0/0 | 2499 | 9 | 9 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0011 | 0/0 | 2497 | 8 | 0 | 0 | 7 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0012 | 0/0 | 2498 | 5 | 0 | 2 | 3 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0013 | 0/0 | 2497 | 5 | 3 | 1 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0014 | 0/0 | 2502 | 5 | 5 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0015 | 0/0 | 2499 | 4 | 1 | 2 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0016 | 0/0 | 2496 | 4 | 2 | 1 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0017 | 0/0 | 2498 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0018 | 0/0 | 2498 | 3 | 0 | 0 | 2 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0019 | 0/0 | 2501 | 2 | 1 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0020 | 0/0 | 2499 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0021 | 0/0 | 2500 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0022 | 0/0 | 2496 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0023 | 0/0 | 2496 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0024 | 0/0 | 2500 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0025 | 0/0 | 2501 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0026 | 0/0 | 2497 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0027 | 0/0 | 2497 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0028 | 0/0 | 2497 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0029 | 0/0 | 2498 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
t0030 | 0/0 | 2498 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
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 | 6 | 0 | 0 | 5 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0002 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0005 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0006 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0010 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0013 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0017 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0299 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4536 | 93 | 26 | 26 | 21 | 6 | 14 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0005 | 0/0 | 4536 | 26 | 5 | 0 | 18 | 0 | 3 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0006 | 0/0 | 4536 | 21 | 3 | 3 | 12 | 2 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0008 | 0/0 | 4536 | 5 | 5 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0011 | 0/0 | 4536 | 4 | 3 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0003 | 1/0 | 4539 | 80 | 16 | 10 | 47 | 1 | 5 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0004 | 0/0 | 4539 | 45 | 3 | 8 | 26 | 1 | 7 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0007 | 0/0 | 4539 | 8 | 1 | 7 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0003c0002 | 0/0 | 4536 | 82 | 15 | 8 | 44 | 2 | 13 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0003c0009 | 0/0 | 4536 | 4 | 3 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0004c0012 | 0/0 | 4536 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0004c0015 | 0/0 | 4536 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0005c0010 | 0/0 | 4536 | 4 | 0 | 3 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0006c0013 | 0/1 | 4536 | 2 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0007c0018 | 0/0 | 4539 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0008c0019 | 0/0 | 4539 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0009c0016 | 0/0 | 4536 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0010c0020 | 0/0 | 4539 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0011c0017 | 0/0 | 4536 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0012c0014 | 0/0 | 4539 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 7032 | 68 | 11 | 25 | 13 | 6 | 13 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0001t0008 | 0/0 | 7033 | 9 | 3 | 0 | 6 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0001t0009 | 0/0 | 7035 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0001t0010 | 0/0 | 7034 | 9 | 9 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0001t0016 | 0/0 | 7031 | 3 | 1 | 1 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0001t0017 | 0/0 | 7033 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0001t0026 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0001t0028 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0005t0001 | 0/0 | 7033 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0005t0004 | 0/0 | 7035 | 15 | 0 | 0 | 13 | 0 | 2 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0005t0005 | 0/0 | 7034 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0005t0012 | 0/0 | 7033 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0005t0014 | 0/0 | 7037 | 5 | 5 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0005t0021 | 0/0 | 7035 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0006t0001 | 0/0 | 7033 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0006t0004 | 0/0 | 7035 | 16 | 3 | 2 | 8 | 2 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0006t0005 | 0/0 | 7034 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0008t0009 | 0/0 | 7035 | 4 | 4 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0008t0017 | 0/0 | 7033 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0011t0009 | 0/0 | 7035 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0001c0011t0025 | 0/0 | 7036 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0003t0001 | 0/0 | 7036 | 40 | 12 | 4 | 19 | 1 | 4 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0003t0005 | 0/0 | 7037 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0003t0006 | 1/0 | 7036 | 19 | 0 | 0 | 18 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0003t0007 | 0/0 | 7035 | 7 | 0 | 1 | 6 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0003t0013 | 0/0 | 7035 | 4 | 3 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0003t0018 | 0/0 | 7036 | 2 | 0 | 0 | 1 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0003t0020 | 0/0 | 7037 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0003t0023 | 0/0 | 7034 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0003t0027 | 0/0 | 7035 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0003t0029 | 0/0 | 7036 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0003t0030 | 0/0 | 7036 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0004t0001 | 0/0 | 7036 | 20 | 3 | 3 | 12 | 1 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0004t0004 | 0/0 | 7038 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0004t0005 | 0/0 | 7037 | 19 | 0 | 3 | 11 | 0 | 5 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0004t0006 | 0/0 | 7036 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0004t0015 | 0/0 | 7037 | 3 | 0 | 2 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0002c0007t0001 | 0/0 | 7036 | 8 | 1 | 7 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0003c0002t0001 | 0/0 | 7033 | 4 | 2 | 0 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0003c0002t0003 | 0/0 | 7031 | 53 | 0 | 6 | 35 | 2 | 10 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0003c0002t0004 | 0/0 | 7035 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0003c0002t0005 | 0/0 | 7034 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0003c0002t0007 | 0/0 | 7032 | 9 | 9 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0003c0002t0009 | 0/0 | 7035 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0003c0002t0011 | 0/0 | 7032 | 8 | 0 | 0 | 7 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0003c0002t0012 | 0/0 | 7033 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0003c0002t0013 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0003c0002t0017 | 0/0 | 7033 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0003c0002t0022 | 0/0 | 7031 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0003c0009t0015 | 0/0 | 7034 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0003c0009t0019 | 0/0 | 7036 | 2 | 1 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0003c0009t0024 | 0/0 | 7035 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0004c0012t0008 | 0/0 | 7033 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0004c0012t0016 | 0/0 | 7031 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0004c0015t0008 | 0/0 | 7033 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0005c0010t0004 | 0/0 | 7035 | 4 | 0 | 3 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0006c0013t0002 | 0/1 | 7032 | 2 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0007c0018t0005 | 0/0 | 7037 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0008c0019t0005 | 0/0 | 7037 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0009c0016t0002 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0010c0020t0018 | 0/0 | 7036 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0011c0017t0002 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
a0012c0014t0005 | 0/0 | 7037 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | copy fasta | chr5 | 56810549 | 56901152 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0005 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0010 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0008g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0008g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0008g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0008g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0008g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0008g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0008g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0008g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0008g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0009g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0010g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0010g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0010g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0010g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0010g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0010g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0010g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0010g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0016g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0016g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0016g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0017g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0026g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0001t0028g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0012g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0012g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0012g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0014g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0014g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0014g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0014g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0014g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0005t0021g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0004g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0004g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0005g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0006t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0008t0009g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0008t0009g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0008t0009g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0008t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0008t0017g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0011t0009g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0011t0009g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0011t0009g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0001c0011t0025g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0005g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0006g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0006g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0006g0017 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0006g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0007g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0007g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0007g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0007g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0007g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0013g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0013g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0013g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0018g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0018g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0020g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0020g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0023g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0027g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0029g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0003t0030g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0005g0001 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0005g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0005g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0005g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0005g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0015g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0015g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0004t0015g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0007t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0007t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0007t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0007t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0007t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0007t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0002c0007t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0007g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0009g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0011g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0011g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0011g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0011g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0011g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0011g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0011g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0011g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0012g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0013g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0017g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0002t0022g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0009t0015g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0009t0019g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0009t0019g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0003c0009t0024g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0004c0012t0008g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0004c0012t0008g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0004c0012t0016g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0004c0015t0008g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0005c0010t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0005c0010t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0005c0010t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0005c0010t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0006c0013t0002g0299 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0006c0013t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0007c0018t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0008c0019t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0009c0016t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0010c0020t0018g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0011c0017t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
a0012c0014t0005g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0002 | t0003 | g0196 | EUR | GBR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0264 | EUR | FIN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00280 | hp2 | a0002 | c0004 | t0001 | g0044 | EUR | FIN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00423 | hp1 | a0002 | c0003 | t0007 | g0016 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00423 | hp2 | a0001 | c0006 | t0005 | g0009 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00438 | hp1 | a0001 | c0001 | t0008 | g0274 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00438 | hp2 | a0003 | c0002 | t0003 | g0008 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00544 | hp1 | a0002 | c0003 | t0006 | g0004 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00544 | hp2 | a0002 | c0004 | t0004 | g0077 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00558 | hp1 | a0003 | c0002 | t0003 | g0011 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00558 | hp2 | a0002 | c0003 | t0029 | g0003 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00597 | hp1 | a0002 | c0003 | t0006 | g0004 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00597 | hp2 | a0003 | c0002 | t0011 | g0173 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00609 | hp2 | a0002 | c0003 | t0007 | g0116 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00621 | hp1 | a0003 | c0002 | t0003 | g0157 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00621 | hp2 | a0002 | c0004 | t0001 | g0107 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00639 | hp1 | a0003 | c0002 | t0003 | g0165 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00642 | hp1 | a0002 | c0003 | t0001 | g0059 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00642 | hp2 | a0006 | c0013 | t0002 | g0302 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00673 | hp1 | a0003 | c0002 | t0003 | g0155 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00673 | hp2 | a0001 | c0005 | t0001 | g0235 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00738 | hp1 | a0002 | c0004 | t0001 | g0078 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG00741 | hp2 | a0002 | c0003 | t0023 | g0120 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01069 | hp1 | a0002 | c0004 | t0001 | g0075 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01069 | hp2 | a0003 | c0002 | t0012 | g0020 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01071 | hp1 | a0003 | c0002 | t0012 | g0020 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01081 | hp1 | a0002 | c0007 | t0001 | g0053 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01081 | hp2 | a0001 | c0011 | t0025 | g0205 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01109 | hp2 | a0003 | c0002 | t0003 | g0189 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01167 | hp2 | a0002 | c0003 | t0013 | g0054 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01168 | hp1 | a0002 | c0004 | t0015 | g0083 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01168 | hp2 | a0003 | c0002 | t0003 | g0195 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01169 | hp1 | a0002 | c0004 | t0015 | g0067 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01192 | hp1 | a0003 | c0002 | t0003 | g0198 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01243 | hp2 | a0003 | c0009 | t0019 | g0326 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01255 | hp1 | a0003 | c0002 | t0003 | g0008 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01256 | hp1 | a0002 | c0004 | t0001 | g0148 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01261 | hp1 | a0001 | c0006 | t0001 | g0245 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01261 | hp2 | a0002 | c0003 | t0007 | g0055 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01346 | hp1 | a0002 | c0003 | t0001 | g0061 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01361 | hp1 | a0002 | c0007 | t0001 | g0096 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01361 | hp2 | a0001 | c0006 | t0004 | g0249 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01433 | hp1 | a0001 | c0006 | t0004 | g0251 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01433 | hp2 | a0002 | c0007 | t0001 | g0014 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01496 | hp1 | a0002 | c0003 | t0005 | g0060 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01496 | hp2 | a0003 | c0002 | t0003 | g0002 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01516 | hp1 | a0001 | c0006 | t0004 | g0023 | EUR | IBS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0307 | EUR | IBS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01517 | hp1 | a0001 | c0006 | t0004 | g0023 | EUR | IBS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0298 | EUR | IBS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01884 | hp1 | a0002 | c0003 | t0001 | g0144 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01884 | hp2 | a0001 | c0005 | t0014 | g0325 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01891 | hp1 | a0001 | c0001 | t0016 | g0313 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01891 | hp2 | a0003 | c0002 | t0004 | g0038 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01928 | hp1 | a0005 | c0010 | t0004 | g0257 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01928 | hp2 | a0002 | c0003 | t0020 | g0134 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01934 | hp2 | a0002 | c0007 | t0001 | g0098 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01943 | hp1 | a0005 | c0010 | t0004 | g0256 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01943 | hp2 | a0002 | c0004 | t0005 | g0073 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0316 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01978 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0305 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01981 | hp2 | a0002 | c0004 | t0005 | g0080 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01993 | hp1 | a0002 | c0007 | t0001 | g0095 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02015 | hp1 | a0002 | c0004 | t0004 | g0122 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02015 | hp2 | a0010 | c0020 | t0018 | g0131 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02040 | hp1 | a0002 | c0003 | t0001 | g0118 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02040 | hp2 | a0002 | c0003 | t0001 | g0097 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02055 | hp2 | a0002 | c0003 | t0027 | g0099 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02056 | hp1 | a0002 | c0003 | t0006 | g0004 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02056 | hp2 | a0001 | c0006 | t0005 | g0253 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02071 | hp1 | a0002 | c0004 | t0005 | g0013 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02071 | hp2 | a0002 | c0003 | t0005 | g0115 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02080 | hp1 | a0001 | c0005 | t0004 | g0230 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02080 | hp2 | a0002 | c0004 | t0005 | g0074 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02083 | hp1 | a0003 | c0002 | t0003 | g0161 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02083 | hp2 | a0002 | c0004 | t0005 | g0071 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02129 | hp1 | a0001 | c0001 | t0008 | g0200 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02129 | hp2 | a0002 | c0004 | t0005 | g0001 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02132 | hp1 | a0003 | c0002 | t0003 | g0166 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02132 | hp2 | a0002 | c0003 | t0007 | g0117 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02135 | hp1 | a0003 | c0002 | t0011 | g0163 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02135 | hp2 | a0001 | c0006 | t0005 | g0009 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02145 | hp1 | a0004 | c0012 | t0016 | g0057 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02145 | hp2 | a0001 | c0001 | t0009 | g0335 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02148 | hp1 | a0002 | c0004 | t0005 | g0006 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02148 | hp2 | a0002 | c0003 | t0020 | g0135 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02155 | hp1 | a0001 | c0006 | t0005 | g0009 | EAS | CDX | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02155 | hp2 | a0003 | c0002 | t0003 | g0154 | EAS | CDX | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02273 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0285 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02293 | hp1 | a0002 | c0007 | t0001 | g0014 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02293 | hp2 | a0005 | c0010 | t0004 | g0259 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02300 | hp1 | a0002 | c0007 | t0001 | g0087 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02300 | hp2 | a0001 | c0001 | t0016 | g0026 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02451 | hp1 | a0001 | c0005 | t0014 | g0324 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02523 | hp1 | a0003 | c0002 | t0011 | g0002 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02523 | hp2 | a0002 | c0003 | t0006 | g0140 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02572 | hp1 | a0001 | c0001 | t0010 | g0029 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02572 | hp2 | a0002 | c0004 | t0001 | g0006 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02615 | hp1 | a0002 | c0004 | t0001 | g0013 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02615 | hp2 | a0003 | c0002 | t0007 | g0041 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02622 | hp1 | a0002 | c0004 | t0001 | g0103 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02622 | hp2 | a0003 | c0002 | t0009 | g0036 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02630 | hp1 | a0003 | c0002 | t0007 | g0012 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02630 | hp2 | a0004 | c0012 | t0008 | g0058 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0317 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02647 | hp2 | a0002 | c0003 | t0001 | g0145 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02683 | hp1 | a0002 | c0003 | t0001 | g0085 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0277 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02698 | hp2 | a0001 | c0005 | t0005 | g0239 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02717 | hp1 | a0001 | c0011 | t0009 | g0206 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02717 | hp2 | a0003 | c0002 | t0007 | g0042 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02723 | hp1 | a0001 | c0005 | t0014 | g0323 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02723 | hp2 | a0001 | c0011 | t0009 | g0204 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02735 | hp2 | a0002 | c0004 | t0005 | g0047 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02738 | hp1 | a0003 | c0002 | t0003 | g0188 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02738 | hp2 | a0011 | c0017 | t0002 | g0311 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02809 | hp1 | a0001 | c0008 | t0009 | g0208 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02818 | hp1 | a0001 | c0001 | t0008 | g0217 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0300 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02886 | hp2 | a0001 | c0001 | t0010 | g0333 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02895 | hp2 | a0002 | c0003 | t0001 | g0048 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02896 | hp1 | a0002 | c0003 | t0001 | g0146 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02896 | hp2 | a0003 | c0002 | t0005 | g0037 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02897 | hp2 | a0002 | c0003 | t0001 | g0019 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02965 | hp1 | a0002 | c0003 | t0001 | g0091 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02965 | hp2 | a0001 | c0001 | t0010 | g0331 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02970 | hp1 | a0002 | c0003 | t0001 | g0052 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0334 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02976 | hp1 | a0002 | c0003 | t0013 | g0125 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02976 | hp2 | a0003 | c0009 | t0019 | g0327 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03017 | hp1 | a0002 | c0003 | t0001 | g0090 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03041 | hp1 | a0003 | c0002 | t0007 | g0012 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03041 | hp2 | a0001 | c0005 | t0014 | g0322 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03098 | hp1 | a0003 | c0002 | t0001 | g0031 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03098 | hp2 | a0004 | c0015 | t0008 | g0216 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03139 | hp1 | a0003 | c0009 | t0015 | g0028 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03139 | hp2 | a0003 | c0002 | t0007 | g0039 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03195 | hp1 | a0003 | c0002 | t0001 | g0030 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03195 | hp2 | a0003 | c0009 | t0024 | g0028 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03209 | hp1 | a0001 | c0011 | t0009 | g0207 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03209 | hp2 | a0002 | c0003 | t0001 | g0019 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03225 | hp1 | a0001 | c0008 | t0009 | g0209 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03225 | hp2 | a0001 | c0001 | t0008 | g0314 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03239 | hp1 | a0003 | c0002 | t0022 | g0002 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03239 | hp2 | a0001 | c0005 | t0004 | g0233 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03453 | hp2 | a0001 | c0001 | t0010 | g0029 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03486 | hp1 | a0003 | c0002 | t0007 | g0035 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03486 | hp2 | a0001 | c0001 | t0010 | g0336 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03491 | hp2 | a0002 | c0004 | t0001 | g0072 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03492 | hp2 | a0002 | c0004 | t0005 | g0076 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03540 | hp1 | a0001 | c0008 | t0009 | g0210 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03540 | hp2 | a0001 | c0001 | t0010 | g0329 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03579 | hp1 | a0002 | c0003 | t0013 | g0089 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03579 | hp2 | a0001 | c0001 | t0017 | g0328 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03654 | hp1 | a0003 | c0002 | t0013 | g0199 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0263 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03669 | hp1 | a0003 | c0002 | t0003 | g0152 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03669 | hp2 | a0002 | c0003 | t0018 | g0127 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03688 | hp1 | a0003 | c0002 | t0003 | g0177 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03688 | hp2 | a0009 | c0016 | t0002 | g0287 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03704 | hp1 | a0002 | c0004 | t0005 | g0106 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03704 | hp2 | a0001 | c0006 | t0004 | g0260 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0297 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03710 | hp2 | a0002 | c0003 | t0001 | g0093 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0269 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03831 | hp2 | a0001 | c0005 | t0004 | g0237 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03834 | hp1 | a0002 | c0004 | t0005 | g0123 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03834 | hp2 | a0003 | c0002 | t0003 | g0162 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03927 | hp1 | a0003 | c0002 | t0003 | g0153 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03927 | hp2 | a0001 | c0001 | t0028 | g0312 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03942 | hp1 | a0003 | c0002 | t0011 | g0192 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03942 | hp2 | a0012 | c0014 | t0005 | g0082 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG04115 | hp1 | a0002 | c0004 | t0015 | g0102 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG04115 | hp2 | a0003 | c0002 | t0003 | g0186 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0315 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG04184 | hp2 | a0002 | c0003 | t0001 | g0112 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG04199 | hp2 | a0003 | c0002 | t0003 | g0193 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG04204 | hp1 | a0003 | c0002 | t0003 | g0185 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG04204 | hp2 | a0003 | c0002 | t0003 | g0151 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG04228 | hp1 | a0003 | c0002 | t0003 | g0187 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0289 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18522 | hp1 | a0002 | c0003 | t0001 | g0046 | AFR | YRI | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18522 | hp2 | a0003 | c0002 | t0007 | g0040 | AFR | YRI | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18612 | hp1 | a0003 | c0002 | t0011 | g0158 | EAS | CHB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18612 | hp2 | a0002 | c0003 | t0001 | g0015 | EAS | CHB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18942 | hp1 | a0002 | c0003 | t0030 | g0126 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18942 | hp2 | a0003 | c0002 | t0001 | g0171 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18945 | hp1 | a0003 | c0002 | t0003 | g0021 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18945 | hp2 | a0001 | c0005 | t0004 | g0229 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18946 | hp1 | a0003 | c0002 | t0001 | g0174 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18946 | hp2 | a0002 | c0004 | t0001 | g0050 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18947 | hp1 | a0002 | c0004 | t0001 | g0109 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18947 | hp2 | a0003 | c0002 | t0011 | g0008 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18948 | hp1 | a0001 | c0005 | t0012 | g0224 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18948 | hp2 | a0002 | c0004 | t0005 | g0081 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18953 | hp2 | a0002 | c0003 | t0006 | g0137 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18956 | hp1 | a0001 | c0006 | t0004 | g0254 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18956 | hp2 | a0003 | c0002 | t0003 | g0168 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18957 | hp1 | a0003 | c0002 | t0003 | g0181 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18957 | hp2 | a0002 | c0004 | t0001 | g0068 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18959 | hp1 | a0002 | c0004 | t0001 | g0064 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18959 | hp2 | a0001 | c0005 | t0004 | g0228 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18960 | hp1 | a0001 | c0001 | t0026 | g0272 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18960 | hp2 | a0001 | c0005 | t0004 | g0232 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18961 | hp1 | a0002 | c0003 | t0006 | g0084 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18961 | hp2 | a0002 | c0003 | t0001 | g0129 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18962 | hp1 | a0001 | c0001 | t0016 | g0275 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18962 | hp2 | a0002 | c0003 | t0006 | g0007 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18963 | hp1 | a0003 | c0002 | t0003 | g0191 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18964 | hp1 | a0003 | c0002 | t0003 | g0032 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18964 | hp2 | a0002 | c0004 | t0001 | g0066 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18965 | hp1 | a0002 | c0003 | t0001 | g0100 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18965 | hp2 | a0003 | c0002 | t0003 | g0033 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18966 | hp1 | a0002 | c0004 | t0001 | g0149 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18966 | hp2 | a0002 | c0003 | t0001 | g0110 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18968 | hp1 | a0001 | c0005 | t0004 | g0236 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18968 | hp2 | a0002 | c0003 | t0001 | g0111 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18969 | hp1 | a0001 | c0006 | t0004 | g0244 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18969 | hp2 | a0002 | c0004 | t0001 | g0143 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18971 | hp1 | a0002 | c0003 | t0006 | g0017 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18972 | hp1 | a0001 | c0006 | t0004 | g0241 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18972 | hp2 | a0002 | c0003 | t0007 | g0015 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18973 | hp1 | a0003 | c0002 | t0003 | g0150 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18973 | hp2 | a0002 | c0004 | t0005 | g0001 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18974 | hp1 | a0003 | c0002 | t0003 | g0011 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18974 | hp2 | a0002 | c0003 | t0001 | g0049 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18975 | hp1 | a0002 | c0004 | t0005 | g0001 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18975 | hp2 | a0003 | c0002 | t0003 | g0180 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18977 | hp1 | a0003 | c0002 | t0003 | g0179 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18977 | hp2 | a0002 | c0004 | t0001 | g0079 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18979 | hp1 | a0002 | c0003 | t0006 | g0136 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18979 | hp2 | a0003 | c0002 | t0003 | g0160 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18981 | hp2 | a0001 | c0005 | t0004 | g0022 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18982 | hp1 | a0003 | c0002 | t0003 | g0167 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18982 | hp2 | a0001 | c0005 | t0004 | g0226 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18983 | hp1 | a0002 | c0003 | t0006 | g0132 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18983 | hp2 | a0003 | c0002 | t0003 | g0002 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18985 | hp1 | a0001 | c0005 | t0004 | g0231 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18985 | hp2 | a0002 | c0003 | t0001 | g0119 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18986 | hp1 | a0003 | c0002 | t0003 | g0183 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18986 | hp2 | a0002 | c0003 | t0001 | g0065 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18987 | hp1 | a0002 | c0003 | t0006 | g0130 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18989 | hp1 | a0003 | c0002 | t0003 | g0172 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18989 | hp2 | a0002 | c0004 | t0001 | g0062 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18990 | hp1 | a0002 | c0003 | t0001 | g0139 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18990 | hp2 | a0002 | c0004 | t0006 | g0070 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18992 | hp1 | a0003 | c0002 | t0003 | g0169 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18992 | hp2 | a0002 | c0004 | t0005 | g0001 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18993 | hp1 | a0003 | c0002 | t0011 | g0194 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18993 | hp2 | a0001 | c0001 | t0008 | g0203 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18995 | hp2 | a0002 | c0003 | t0006 | g0004 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18998 | hp1 | a0003 | c0002 | t0003 | g0002 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18998 | hp2 | a0001 | c0006 | t0004 | g0250 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18999 | hp1 | a0003 | c0002 | t0003 | g0164 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18999 | hp2 | a0002 | c0004 | t0005 | g0001 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19001 | hp1 | a0001 | c0005 | t0004 | g0238 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19001 | hp2 | a0002 | c0003 | t0007 | g0016 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19002 | hp1 | a0005 | c0010 | t0004 | g0258 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19002 | hp2 | a0007 | c0018 | t0005 | g0063 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19003 | hp1 | a0001 | c0005 | t0004 | g0234 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19003 | hp2 | a0003 | c0002 | t0003 | g0156 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19005 | hp1 | a0003 | c0002 | t0011 | g0176 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19005 | hp2 | a0001 | c0001 | t0008 | g0278 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19006 | hp1 | a0003 | c0002 | t0003 | g0182 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19006 | hp2 | a0001 | c0006 | t0004 | g0243 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19007 | hp1 | a0001 | c0005 | t0004 | g0022 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19007 | hp2 | a0002 | c0003 | t0006 | g0142 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19009 | hp1 | a0003 | c0002 | t0003 | g0021 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19009 | hp2 | a0001 | c0005 | t0021 | g0240 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19011 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19011 | hp2 | a0003 | c0002 | t0003 | g0190 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19012 | hp1 | a0002 | c0003 | t0001 | g0121 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19043 | hp1 | a0001 | c0008 | t0009 | g0212 | AFR | LWK | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19043 | hp2 | a0001 | c0005 | t0014 | g0321 | AFR | LWK | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19054 | hp1 | a0001 | c0006 | t0004 | g0255 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19054 | hp2 | a0001 | c0001 | t0008 | g0201 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19056 | hp1 | a0003 | c0002 | t0003 | g0159 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19056 | hp2 | a0002 | c0003 | t0006 | g0007 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19057 | hp1 | a0008 | c0019 | t0005 | g0069 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19057 | hp2 | a0002 | c0003 | t0006 | g0007 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19058 | hp1 | a0002 | c0003 | t0001 | g0124 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19060 | hp1 | a0003 | c0002 | t0003 | g0002 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19060 | hp2 | a0001 | c0005 | t0012 | g0222 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19063 | hp1 | a0001 | c0006 | t0004 | g0246 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19063 | hp2 | a0002 | c0004 | t0001 | g0108 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19068 | hp1 | a0002 | c0003 | t0006 | g0138 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19068 | hp2 | a0003 | c0002 | t0003 | g0170 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19076 | hp1 | a0001 | c0005 | t0012 | g0223 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19076 | hp2 | a0002 | c0003 | t0001 | g0104 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19077 | hp1 | a0003 | c0002 | t0003 | g0178 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19077 | hp2 | a0002 | c0003 | t0001 | g0051 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19078 | hp2 | a0002 | c0004 | t0005 | g0113 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19079 | hp2 | a0002 | c0003 | t0001 | g0105 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19080 | hp1 | a0001 | c0005 | t0004 | g0225 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19080 | hp2 | a0003 | c0002 | t0003 | g0175 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19081 | hp1 | a0002 | c0003 | t0007 | g0114 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19084 | hp1 | a0002 | c0003 | t0001 | g0128 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19084 | hp2 | a0002 | c0003 | t0018 | g0086 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19085 | hp2 | a0002 | c0004 | t0001 | g0045 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19088 | hp1 | a0002 | c0004 | t0005 | g0006 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19088 | hp2 | a0001 | c0005 | t0004 | g0227 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19090 | hp1 | a0002 | c0003 | t0006 | g0133 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19090 | hp2 | a0001 | c0001 | t0008 | g0202 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19091 | hp1 | a0002 | c0003 | t0006 | g0101 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19091 | hp2 | a0002 | c0003 | t0001 | g0141 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19240 | hp1 | a0003 | c0002 | t0017 | g0215 | AFR | YRI | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA19240 | hp2 | a0003 | c0002 | t0007 | g0034 | AFR | YRI | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA20129 | hp1 | a0002 | c0003 | t0001 | g0018 | AFR | ASW | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA20129 | hp2 | a0002 | c0007 | t0001 | g0094 | AFR | ASW | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0296 | EUR | TSI | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0214 | EUR | TSI | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA20805 | hp1 | a0002 | c0003 | t0001 | g0147 | EUR | TSI | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA20805 | hp2 | a0003 | c0002 | t0003 | g0197 | EUR | TSI | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA20905 | hp1 | a0002 | c0004 | t0005 | g0001 | SAS | GIH | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | GIH | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02109 | hp1 | a0001 | c0006 | t0004 | g0252 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02109 | hp2 | a0004 | c0012 | t0008 | g0056 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02486 | hp1 | a0001 | c0006 | t0004 | g0247 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02486 | hp2 | a0002 | c0003 | t0001 | g0018 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02559 | hp1 | a0002 | c0003 | t0001 | g0092 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG02559 | hp2 | a0003 | c0002 | t0007 | g0043 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03471 | hp1 | a0001 | c0001 | t0010 | g0330 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG03471 | hp2 | a0001 | c0008 | t0017 | g0211 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG06807 | hp1 | a0001 | c0006 | t0004 | g0248 | AFR | USA | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | USA | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18955 | hp1 | a0003 | c0002 | t0003 | g0184 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA18955 | hp2 | a0001 | c0006 | t0004 | g0242 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA20300 | hp1 | a0001 | c0001 | t0010 | g0332 | AFR | USA | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | USA | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | LWK | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
NA21309 | hp2 | a0002 | c0003 | t0013 | g0088 | AFR | LWK | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
homoSapiens_chm13v2 | hp1 | a0006 | c0013 | t0002 | g0299 | REF | REF | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
homoSapiens_grch38 | hp1 | a0002 | c0003 | t0006 | g0017 | REF | REF | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:56815806
|
T | C | 1 | a0005 | 4 | HG01928.hp1 HG01943.hp1 HG02293.hp2 others(1): Show |
missense_variant | MODERATE | c.233T>C | p.Leu78Pro | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/20 | 258/7036 | 233/4539 | 78/1512 | chr5 | 56815806 | ||
chr5:56815877
|
G | A | 1 | a0012 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.304G>A | p.Gly102Arg | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/20 | 329/7036 | 304/4539 | 102/1512 | chr5 | 56815877 | ||
chr5:56815967
|
G | C | 1 | a0012 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.394G>C | p.Asp132His | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/20 | 419/7036 | 394/4539 | 132/1512 | chr5 | 56815967 | ||
chr5:56859845
|
A | G | 1 | a0004 | 4 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
missense_variant | MODERATE | c.764A>G | p.Asn255Ser | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/20 | 789/7036 | 764/4539 | 255/1512 | chr5 | 56859845 | ||
chr5:56864836
|
C | T | 1 | a0011 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.937C>T | p.Arg313Trp | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 4/20 | 962/7036 | 937/4539 | 313/1512 | chr5 | 56864836 | ||
chr5:56881185
|
T | C | 1 | a0010 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.2282T>C | p.Ile761Thr | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 13/20 | 2307/7036 | 2282/4539 | 761/1512 | chr5 | 56881185 | ||
chr5:56881616
|
G | A | 6 | a0001a0004a0005others(3): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(158): Show |
missense_variant | MODERATE | c.2416G>A | p.Asp806Asn | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 2441/7036 | 2416/4539 | 806/1512 | chr5 | 56881616 | ||
chr5:56881647
|
C | G | 1 | a0009 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.2447C>G | p.Ser816Cys | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 2472/7036 | 2447/4539 | 816/1512 | chr5 | 56881647 | ||
chr5:56881916
|
G | A | 7 | a0001a0003a0004others(4): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
missense_variant | MODERATE | c.2716G>A | p.Val906Ile | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 2741/7036 | 2716/4539 | 906/1512 | chr5 | 56881916 | ||
chr5:56882016
|
C | G | 1 | a0006 | 2 | HG00642.hp2 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.2816C>G | p.Ser939Cys | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 2841/7036 | 2816/4539 | 939/1512 | chr5 | 56882016 | ||
chr5:56882021
|
TCAA | T | 7 | a0001a0003a0004others(4): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
conservative_inframe_deletion | MODERATE | c.2845_2847delACA | p.Thr949del | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 2870/7036 | 2845/4539 | 949/1512 | INFO_REALIGN_3_PRIME | chr5 | 56882021 | |
chr5:56882315
|
T | C | 1 | a0007 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.3115T>C | p.Ser1039Pro | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 3140/7036 | 3115/4539 | 1039/1512 | chr5 | 56882315 | ||
chr5:56883573
|
G | A | 1 | a0008 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.3713G>A | p.Arg1238Lys | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/20 | 3738/7036 | 3713/4539 | 1238/1512 | chr5 | 56883573 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:56815618
|
G | A | 1 | a0003c0009 | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
synonymous_variant | LOW | c.45G>A | p.Pro15Pro | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/20 | 70/7036 | 45/4539 | 15/1512 | chr5 | 56815618 | ||
chr5:56815654
|
C | T | 1 | a0002c0007 | 8 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(5): Show |
synonymous_variant | LOW | c.81C>T | p.Gly27Gly | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/20 | 106/7036 | 81/4539 | 27/1512 | chr5 | 56815654 | ||
chr5:56815738
|
G | A | 1 | a0003c0009 | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
synonymous_variant | LOW | c.165G>A | p.Ala55Ala | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/20 | 190/7036 | 165/4539 | 55/1512 | chr5 | 56815738 | ||
chr5:56815807
|
C | T | 1 | a0005c0010 | 4 | HG01928.hp1 HG01943.hp1 HG02293.hp2 others(1): Show |
synonymous_variant | LOW | c.234C>T | p.Leu78Leu | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/20 | 259/7036 | 234/4539 | 78/1512 | chr5 | 56815807 | ||
chr5:56815924
|
G | C | 11 | a0001c0001a0001c0005a0001c0006others(8): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
synonymous_variant | LOW | c.351G>C | p.Ala117Ala | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/20 | 376/7036 | 351/4539 | 117/1512 | chr5 | 56815924 | ||
chr5:56859801
|
G | A | 2 | a0004c0012a0004c0015 | 4 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
synonymous_variant | LOW | c.720G>A | p.Ala240Ala | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/20 | 745/7036 | 720/4539 | 240/1512 | chr5 | 56859801 | ||
chr5:56865960
|
G | A | 17 | a0001c0001a0001c0005a0001c0006others(14): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
synonymous_variant | LOW | c.1284G>A | p.Thr428Thr | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/20 | 1309/7036 | 1284/4539 | 428/1512 | chr5 | 56865960 | ||
chr5:56872885
|
C | T | 2 | a0001c0006a0005c0010 | 25 | HG00423.hp2 HG01261.hp1 HG01361.hp2 others(22): Show |
synonymous_variant | LOW | c.1566C>T | p.Thr522Thr | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/20 | 1591/7036 | 1566/4539 | 522/1512 | chr5 | 56872885 | ||
chr5:56872963
|
A | G | 1 | a0003c0009 | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
synonymous_variant | LOW | c.1644A>G | p.Gln548Gln | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/20 | 1669/7036 | 1644/4539 | 548/1512 | chr5 | 56872963 | ||
chr5:56875262
|
G | A | 2 | a0001c0008a0001c0011 | 9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
synonymous_variant | LOW | c.1917G>A | p.Leu639Leu | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/20 | 1942/7036 | 1917/4539 | 639/1512 | chr5 | 56875262 | ||
chr5:56882284
|
A | G | 5 | a0001c0005a0001c0006a0001c0008others(2): Show | 60 | HG00423.hp2 HG00673.hp2 HG01081.hp2 others(57): Show |
synonymous_variant | LOW | c.3084A>G | p.Gln1028Gln | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 3109/7036 | 3084/4539 | 1028/1512 | chr5 | 56882284 | ||
chr5:56882287
|
C | T | 1 | a0001c0011 | 4 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
synonymous_variant | LOW | c.3087C>T | p.Phe1029Phe | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 3112/7036 | 3087/4539 | 1029/1512 | chr5 | 56882287 | ||
chr5:56882390
|
A | C | 13 | a0001c0001a0001c0005a0001c0006others(10): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
synonymous_variant | LOW | c.3190A>C | p.Arg1064Arg | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 3215/7036 | 3190/4539 | 1064/1512 | chr5 | 56882390 | ||
chr5:56882839
|
A | G | 1 | a0004c0015 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.3639A>G | p.Gly1213Gly | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 3664/7036 | 3639/4539 | 1213/1512 | chr5 | 56882839 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:56894072
|
G | T | 1 | a0002c0003t0030 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*392G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 392 | chr5 | 56894072 | |||||
chr5:56894081
|
T | C | 1 | a0001c0005t0021 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*401T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 401 | chr5 | 56894081 | |||||
chr5:56894704
|
G | A | 57 | a0001c0001t0002a0001c0001t0008a0001c0001t0009others(54): Show | 358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
3_prime_UTR_variant | MODIFIER | c.*1024G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1024 | chr5 | 56894704 | |||||
chr5:56895007
|
A | G | 1 | a0002c0003t0029 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1327A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1327 | chr5 | 56895007 | |||||
chr5:56895063
|
G | C | 1 | a0003c0002t0022 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1383G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1383 | chr5 | 56895063 | |||||
chr5:56895159
|
A | G | 22 | a0001c0001t0002a0001c0001t0008a0001c0001t0009others(19): Show | 118 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*1479A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1479 | chr5 | 56895159 | |||||
chr5:56895283
|
G | T | 2 | a0002c0003t0018a0010c0020t0018 | 3 | HG02015.hp2 HG03669.hp2 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1603G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1603 | chr5 | 56895283 | |||||
chr5:56895364
|
TTG | T | 12 | a0001c0001t0002a0001c0001t0008a0001c0001t0016others(9): Show | 91 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1686_*1687delGT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1686 | INFO_REALIGN_3_PRIME | chr5 | 56895364 | ||||
chr5:56895366
|
G | GT | 4 | a0001c0011t0025a0002c0003t0020a0002c0004t0015others(1): Show | 7 | HG01081.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1701dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1702 | INFO_REALIGN_3_PRIME | chr5 | 56895366 | ||||
chr5:56895366
|
G | GTT | 3 | a0001c0005t0014a0003c0009t0019a0003c0009t0024 | 8 | HG01243.hp2 HG01884.hp2 HG02451.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1700_*1701dupTT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1702 | INFO_REALIGN_3_PRIME | chr5 | 56895366 | ||||
chr5:56895366
|
GT | G | 3 | a0002c0003t0013a0002c0003t0023a0003c0002t0013 | 6 | HG00741.hp2 HG01167.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1701delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1701 | INFO_REALIGN_3_PRIME | chr5 | 56895366 | ||||
chr5:56895366
|
GTT | G | 5 | a0001c0005t0012a0003c0002t0003a0003c0002t0011others(2): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1700_*1701delTT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1700 | INFO_REALIGN_3_PRIME | chr5 | 56895366 | ||||
chr5:56895373
|
T | A | 12 | a0001c0001t0002a0001c0001t0008a0001c0001t0016others(9): Show | 91 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1693T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1693 | chr5 | 56895373 | |||||
chr5:56895559
|
T | G | 1 | a0001c0001t0026 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1879T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1879 | chr5 | 56895559 | |||||
chr5:56895634
|
T | C | 1 | a0002c0003t0027 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1954T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1954 | chr5 | 56895634 | |||||
chr5:56895976
|
C | CA | 18 | a0001c0001t0002a0001c0001t0010a0001c0001t0026others(15): Show | 124 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*2314dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 2315 | INFO_REALIGN_3_PRIME | chr5 | 56895976 | ||||
chr5:56895976
|
C | CAA | 17 | a0001c0001t0008a0001c0001t0009a0001c0005t0004others(14): Show | 71 | HG00438.hp1 HG00544.hp2 HG01069.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2313_*2314dupAA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 2315 | INFO_REALIGN_3_PRIME | chr5 | 56895976 | ||||
chr5:56895976
|
CA | C | 3 | a0002c0003t0007a0002c0003t0023a0003c0002t0007 | 17 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2314delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 2314 | INFO_REALIGN_3_PRIME | chr5 | 56895976 | ||||
chr5:56896108
|
T | C | 1 | a0001c0001t0028 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2428T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 2428 | chr5 | 56896108 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:56816100
|
C | T | 150 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(147): Show | 163 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.482+45C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816100 | ||||||
chr5:56816118
|
C | T | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.482+63C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816118 | ||||||
chr5:56816171
|
G | A | 4 | a0001c0001t0008g0200a0001c0001t0008g0201a0001c0001t0008g0202others(1): Show | 4 | HG02129.hp1 NA18993.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+116G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816171 | ||||||
chr5:56816270
|
G | A | 2 | a0003c0002t0001g0030a0003c0002t0001g0031 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.482+215G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816270 | ||||||
chr5:56816462
|
G | A | 4 | a0001c0011t0009g0204a0001c0011t0009g0206a0001c0011t0009g0207others(1): Show | 4 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+407G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816462 | ||||||
chr5:56816554
|
G | T | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+499G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816554 | ||||||
chr5:56816717
|
G | C | 1 | a0001c0011t0009g0204 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.482+662G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816717 | ||||||
chr5:56816718
|
T | A | 1 | a0001c0011t0009g0204 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.482+663T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816718 | ||||||
chr5:56816762
|
G | A | 9 | a0001c0008t0009g0208a0001c0008t0009g0209a0001c0008t0009g0210others(6): Show | 9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+707G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816762 | ||||||
chr5:56816767
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.482+712G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816767 | ||||||
chr5:56816791
|
A | C | 1 | a0003c0002t0013g0199 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.482+736A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816791 | ||||||
chr5:56816824
|
G | A | 3 | a0003c0002t0003g0011a0003c0002t0003g0032a0003c0002t0003g0033 | 4 | HG00558.hp1 NA18964.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+769G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816824 | ||||||
chr5:56816871
|
C | T | 59 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(56): Show | 65 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.482+816C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816871 | ||||||
chr5:56816907
|
C | T | 1 | a0002c0004t0001g0149 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.482+852C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816907 | ||||||
chr5:56817033
|
G | A | 13 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(10): Show | 14 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.482+978G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56817033 | ||||||
chr5:56817087
|
C | T | 4 | a0001c0008t0009g0209a0001c0008t0009g0210a0001c0008t0009g0212others(1): Show | 4 | HG03225.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+1032C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56817087 | ||||||
chr5:56817211
|
CTTGT | C | 7 | a0001c0005t0014g0321a0001c0005t0014g0322a0001c0005t0014g0323others(4): Show | 7 | HG01192.hp1 HG01884.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+1167_482+1170d others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56817211 | |||||
chr5:56817262
|
C | A | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+1207C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56817262 | ||||||
chr5:56817615
|
C | T | 14 | a0003c0002t0003g0185a0003c0002t0003g0186a0003c0002t0003g0187others(11): Show | 14 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.482+1560C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56817615 | ||||||
chr5:56817683
|
T | G | 2 | a0003c0002t0003g0185a0003c0002t0003g0186 | 2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.482+1628T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56817683 | ||||||
chr5:56817736
|
T | A | 1 | a0001c0001t0002g0214 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.482+1681T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56817736 | ||||||
chr5:56817737
|
G | T | 6 | a0003c0002t0007g0012a0003c0002t0007g0039a0003c0002t0007g0040others(3): Show | 7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+1682G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56817737 | ||||||
chr5:56817962
|
G | C | 9 | a0001c0008t0009g0208a0001c0008t0009g0209a0001c0008t0009g0210others(6): Show | 9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+1907G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56817962 | ||||||
chr5:56818023
|
G | T | 73 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(70): Show | 81 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.482+1968G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818023 | ||||||
chr5:56818176
|
G | A | 1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.482+2121G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818176 | ||||||
chr5:56818313
|
C | A | 1 | a0002c0004t0001g0044 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.482+2258C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818313 | ||||||
chr5:56818348
|
G | T | 2 | a0002c0004t0001g0044a0002c0004t0001g0148 | 2 | HG00280.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.482+2293G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818348 | ||||||
chr5:56818435
|
C | T | 1 | a0002c0003t0001g0147 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.482+2380C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818435 | ||||||
chr5:56818594
|
G | A | 1 | a0003c0002t0003g0150 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.482+2539G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818594 | ||||||
chr5:56818699
|
T | G | 84 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(81): Show | 92 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.482+2644T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818699 | ||||||
chr5:56818717
|
G | C | 1 | a0001c0005t0012g0222 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.482+2662G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818717 | ||||||
chr5:56818734
|
A | G | 1 | a0001c0001t0010g0029 | 2 | HG02572.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.482+2679A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818734 | ||||||
chr5:56818756
|
A | G | 13 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(10): Show | 14 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.482+2701A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818756 | ||||||
chr5:56818761
|
A | G | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+2706A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818761 | ||||||
chr5:56818908
|
C | T | 1 | a0001c0001t0002g0320 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.482+2853C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818908 | ||||||
chr5:56818959
|
A | G | 219 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(216): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.482+2904A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818959 | ||||||
chr5:56818993
|
T | C | 1 | a0002c0004t0001g0045 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.482+2938T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818993 | ||||||
chr5:56819023
|
A | G | 9 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(6): Show | 10 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.482+2968A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819023 | ||||||
chr5:56819041
|
TC | T | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.482+2988delC | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56819041 | |||||
chr5:56819158
|
G | A | 1 | a0002c0003t0001g0046 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.482+3103G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819158 | ||||||
chr5:56819209
|
A | G | 219 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(216): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.482+3154A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819209 | ||||||
chr5:56819243
|
G | T | 2 | a0001c0001t0002g0318a0001c0001t0002g0319 | 2 | NA18981.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.482+3188G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819243 | ||||||
chr5:56819438
|
CA | C | 218 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(215): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.482+3393delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56819438 | |||||
chr5:56819525
|
A | G | 3 | a0003c0002t0004g0038a0003c0002t0005g0037a0003c0002t0009g0036 | 3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+3470A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819525 | ||||||
chr5:56819635
|
ATCT | A | 5 | a0002c0003t0001g0018a0002c0003t0001g0019a0002c0003t0001g0144others(2): Show | 7 | HG01884.hp1 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.482+3585_482+3587d others(5): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56819635 | |||||
chr5:56819675
|
T | A | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+3620T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819675 | ||||||
chr5:56819707
|
C | G | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+3652C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819707 | ||||||
chr5:56819714
|
C | G | 1 | a0001c0008t0009g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.482+3659C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819714 | ||||||
chr5:56819829
|
A | G | 13 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(10): Show | 14 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.482+3774A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819829 | ||||||
chr5:56819952
|
A | G | 1 | a0001c0006t0004g0260 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.482+3897A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819952 | ||||||
chr5:56820129
|
T | C | 1 | a0001c0011t0025g0205 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.482+4074T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820129 | ||||||
chr5:56820145
|
A | G | 1 | a0001c0008t0009g0208 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.482+4090A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820145 | ||||||
chr5:56820258
|
A | G | 223 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(220): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.482+4203A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820258 | ||||||
chr5:56820277
|
A | G | 2 | a0003c0002t0007g0034a0003c0002t0007g0035 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.482+4222A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820277 | ||||||
chr5:56820319
|
A | G | 1 | a0002c0004t0001g0143 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.482+4264A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820319 | ||||||
chr5:56820384
|
T | G | 20 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(17): Show | 21 | HG00673.hp2 HG02080.hp1 HG02698.hp2 others(18): Show |
intron_variant | MODIFIER | c.482+4329T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820384 | ||||||
chr5:56820424
|
A | G | 3 | a0003c0002t0004g0038a0003c0002t0005g0037a0003c0002t0009g0036 | 3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+4369A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820424 | ||||||
chr5:56820580
|
A | G | 1 | a0001c0011t0025g0205 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.482+4525A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820580 | ||||||
chr5:56820706
|
C | T | 3 | a0003c0002t0003g0182a0003c0002t0003g0183a0003c0002t0003g0184 | 3 | NA18955.hp1 NA18986.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.482+4651C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820706 | ||||||
chr5:56820806
|
T | C | 1 | a0002c0003t0001g0144 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.482+4751T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820806 | ||||||
chr5:56820918
|
C | T | 1 | a0003c0002t0012g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.482+4863C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820918 | ||||||
chr5:56820945
|
C | A | 223 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(220): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.482+4890C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820945 | ||||||
chr5:56821079
|
G | A | 1 | a0001c0001t0002g0261 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.482+5024G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821079 | ||||||
chr5:56821271
|
A | C | 1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.482+5216A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821271 | ||||||
chr5:56821281
|
G | C | 325 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(322): Show | 358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.482+5226G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821281 | ||||||
chr5:56821327
|
G | A | 1 | a0001c0001t0002g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.482+5272G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821327 | ||||||
chr5:56821490
|
G | A | 1 | a0001c0001t0002g0263 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.482+5435G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821490 | ||||||
chr5:56821510
|
A | T | 1 | a0001c0001t0002g0317 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.482+5455A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821510 | ||||||
chr5:56821542
|
A | C | 1 | a0002c0003t0006g0142 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.482+5487A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821542 | ||||||
chr5:56821808
|
C | T | 1 | a0002c0003t0013g0125 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.482+5753C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821808 | ||||||
chr5:56821895
|
A | C | 1 | a0001c0005t0021g0240 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.482+5840A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821895 | ||||||
chr5:56821991
|
T | G | 3 | a0003c0002t0003g0151a0003c0002t0003g0152a0003c0002t0003g0153 | 3 | HG03669.hp1 HG03927.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.482+5936T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821991 | ||||||
chr5:56822013
|
C | T | 9 | a0001c0008t0009g0208a0001c0008t0009g0209a0001c0008t0009g0210others(6): Show | 9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+5958C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56822013 | ||||||
chr5:56822100
|
A | G | 1 | a0002c0003t0001g0124 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.482+6045A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56822100 | ||||||
chr5:56822125
|
A | G | 94 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(91): Show | 103 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.482+6070A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56822125 | ||||||
chr5:56822398
|
A | G | 3 | a0002c0003t0001g0019a0002c0003t0001g0144a0002c0003t0001g0146 | 4 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+6343A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56822398 | ||||||
chr5:56822439
|
G | A | 1 | a0002c0004t0005g0047 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.482+6384G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56822439 | ||||||
chr5:56822509
|
G | A | 1 | a0001c0001t0002g0264 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.482+6454G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56822509 | ||||||
chr5:56822906
|
A | T | 223 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(220): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.482+6851A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56822906 | ||||||
chr5:56822922
|
G | T | 1 | a0001c0005t0005g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.482+6867G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56822922 | ||||||
chr5:56823037
|
A | G | 13 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(10): Show | 14 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.482+6982A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56823037 | ||||||
chr5:56823048
|
G | A | 84 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(81): Show | 92 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.482+6993G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56823048 | ||||||
chr5:56823068
|
C | T | 4 | a0005c0010t0004g0256a0005c0010t0004g0257a0005c0010t0004g0258others(1): Show | 4 | HG01928.hp1 HG01943.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+7013C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56823068 | ||||||
chr5:56823203
|
G | A | 1 | a0003c0002t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.482+7148G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56823203 | ||||||
chr5:56823266
|
C | T | 1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.482+7211C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56823266 | ||||||
chr5:56823363
|
C | A | 84 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(81): Show | 92 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.482+7308C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56823363 | ||||||
chr5:56823649
|
A | G | 2 | a0001c0005t0014g0324a0001c0005t0014g0325 | 2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.482+7594A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56823649 | ||||||
chr5:56824045
|
A | G | 1 | a0001c0001t0002g0261 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.482+7990A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824045 | ||||||
chr5:56824140
|
C | G | 3 | a0003c0002t0004g0038a0003c0002t0005g0037a0003c0002t0009g0036 | 3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+8085C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824140 | ||||||
chr5:56824326
|
G | A | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+8271G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824326 | ||||||
chr5:56824419
|
T | C | 1 | a0001c0005t0005g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.482+8364T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824419 | ||||||
chr5:56824523
|
A | C | 5 | a0002c0003t0001g0018a0002c0003t0001g0019a0002c0003t0001g0144others(2): Show | 7 | HG01884.hp1 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.482+8468A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824523 | ||||||
chr5:56824528
|
A | G | 45 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(42): Show | 51 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.482+8473A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824528 | ||||||
chr5:56824546
|
G | A | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.482+8491G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824546 | ||||||
chr5:56824586
|
C | T | 219 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(216): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.482+8531C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824586 | ||||||
chr5:56824597
|
A | G | 1 | a0002c0004t0005g0123 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.482+8542A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824597 | ||||||
chr5:56824625
|
T | G | 1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.482+8570T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824625 | ||||||
chr5:56824819
|
G | A | 84 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(81): Show | 92 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.482+8764G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824819 | ||||||
chr5:56824859
|
T | C | 84 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(81): Show | 92 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.482+8804T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824859 | ||||||
chr5:56824919
|
C | G | 3 | a0001c0005t0004g0236a0001c0005t0004g0237a0001c0005t0004g0238 | 3 | HG03831.hp2 NA18968.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.482+8864C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824919 | ||||||
chr5:56824933
|
T | A | 1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.482+8878T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824933 | ||||||
chr5:56824942
|
T | A | 218 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(215): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.482+8887T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824942 | ||||||
chr5:56824943
|
T | A | 157 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(154): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.482+8888T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824943 | ||||||
chr5:56824967
|
G | A | 1 | a0001c0001t0002g0265 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.482+8912G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824967 | ||||||
chr5:56824976
|
A | G | 1 | a0001c0001t0002g0317 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.482+8921A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824976 | ||||||
chr5:56825170
|
A | G | 1 | a0001c0001t0002g0213 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.482+9115A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825170 | ||||||
chr5:56825304
|
T | C | 223 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(220): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.482+9249T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825304 | ||||||
chr5:56825416
|
G | A | 1 | a0001c0001t0002g0266 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.482+9361G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825416 | ||||||
chr5:56825635
|
T | C | 3 | a0003c0002t0004g0038a0003c0002t0005g0037a0003c0002t0009g0036 | 3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+9580T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825635 | ||||||
chr5:56825785
|
C | T | 1 | a0002c0004t0004g0122 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.482+9730C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825785 | ||||||
chr5:56825821
|
C | A | 1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.482+9766C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825821 | ||||||
chr5:56825927
|
A | G | 223 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(220): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.482+9872A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825927 | ||||||
chr5:56825959
|
C | T | 3 | a0001c0011t0025g0205a0003c0002t0003g0195a0003c0002t0003g0196 | 3 | HG00099.hp1 HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.482+9904C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825959 | ||||||
chr5:56825961
|
G | C | 219 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(216): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.482+9906G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825961 | ||||||
chr5:56825967
|
CT | C | 64 | a0001c0001t0002g0267a0002c0003t0001g0048a0002c0003t0001g0049others(61): Show | 71 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.482+9924delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56825967 | |||||
chr5:56826006
|
T | G | 1 | a0002c0004t0001g0050 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.482+9951T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56826006 | ||||||
chr5:56826395
|
G | C | 1 | a0001c0001t0002g0268 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.482+10340G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56826395 | ||||||
chr5:56826475
|
C | CA | 3 | a0001c0005t0012g0222a0001c0005t0012g0223a0001c0005t0012g0224 | 3 | NA18948.hp1 NA19060.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.482+10421dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56826475 | |||||
chr5:56826489
|
CAGGGAA | C | 84 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(81): Show | 92 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.482+10436_482+1044 others(10): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56826489 | |||||
chr5:56826517
|
A | G | 42 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(39): Show | 46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.482+10462A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56826517 | ||||||
chr5:56826529
|
T | A | 1 | a0002c0003t0001g0051 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.482+10474T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56826529 | ||||||
chr5:56826664
|
C | T | 2 | a0001c0006t0004g0254a0001c0006t0004g0255 | 2 | NA18956.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.482+10609C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56826664 | ||||||
chr5:56826749
|
G | A | 6 | a0003c0002t0007g0012a0003c0002t0007g0039a0003c0002t0007g0040others(3): Show | 7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+10694G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56826749 | ||||||
chr5:56826817
|
G | T | 1 | a0003c0002t0003g0181 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.482+10762G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56826817 | ||||||
chr5:56827064
|
G | A | 1 | a0003c0002t0003g0187 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.482+11009G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827064 | ||||||
chr5:56827096
|
C | T | 1 | a0001c0001t0017g0328 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.482+11041C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827096 | ||||||
chr5:56827189
|
A | AGCTG | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.482+11136_482+1113 others(8): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56827189 | |||||
chr5:56827218
|
G | A | 1 | a0002c0003t0001g0052 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.482+11163G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827218 | ||||||
chr5:56827231
|
G | A | 9 | a0001c0008t0009g0208a0001c0008t0009g0209a0001c0008t0009g0210others(6): Show | 9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+11176G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827231 | ||||||
chr5:56827260
|
C | T | 1 | a0003c0002t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.482+11205C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827260 | ||||||
chr5:56827282
|
C | T | 1 | a0003c0002t0001g0031 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.482+11227C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827282 | ||||||
chr5:56827605
|
C | T | 84 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(81): Show | 92 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.482+11550C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827605 | ||||||
chr5:56827616
|
T | C | 337 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(334): Show | 372 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.482+11561T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827616 | ||||||
chr5:56827678
|
A | T | 12 | a0002c0003t0001g0015a0002c0003t0001g0118a0002c0003t0001g0119others(9): Show | 13 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.482+11623A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827678 | ||||||
chr5:56827752
|
T | C | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+11697T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827752 | ||||||
chr5:56827864
|
C | CA | 13 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(10): Show | 14 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.482+11821dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56827864 | |||||
chr5:56827875
|
A | T | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.482+11820A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827875 | ||||||
chr5:56827919
|
C | T | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.482+11864C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827919 | ||||||
chr5:56828038
|
T | TA | 3 | a0003c0002t0004g0038a0003c0002t0005g0037a0003c0002t0009g0036 | 3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+11984dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56828038 | |||||
chr5:56828130
|
A | G | 2 | a0003c0002t0007g0034a0003c0002t0007g0035 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.482+12075A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828130 | ||||||
chr5:56828197
|
G | A | 1 | a0002c0007t0001g0053 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.482+12142G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828197 | ||||||
chr5:56828284
|
T | C | 223 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(220): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.482+12229T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828284 | ||||||
chr5:56828526
|
A | G | 9 | a0001c0008t0009g0208a0001c0008t0009g0209a0001c0008t0009g0210others(6): Show | 9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+12471A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828526 | ||||||
chr5:56828596
|
T | A | 219 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(216): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.482+12541T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828596 | ||||||
chr5:56828622
|
A | G | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.482+12567A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828622 | ||||||
chr5:56828788
|
G | A | 8 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0007g0012others(5): Show | 9 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.482+12733G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828788 | ||||||
chr5:56828809
|
TA | T | 9 | a0001c0008t0009g0208a0001c0008t0009g0209a0001c0008t0009g0210others(6): Show | 9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+12760delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56828809 | |||||
chr5:56828816
|
G | T | 9 | a0001c0008t0009g0208a0001c0008t0009g0209a0001c0008t0009g0210others(6): Show | 9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+12761G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828816 | ||||||
chr5:56828828
|
ACTT | A | 3 | a0001c0005t0001g0235a0002c0003t0020g0134a0002c0003t0020g0135 | 3 | HG00673.hp2 HG01928.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.482+12780_482+1278 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56828828 | |||||
chr5:56828882
|
CTTTTT | C | 219 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(216): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.482+12833_482+1283 others(9): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56828882 | |||||
chr5:56828902
|
A | G | 2 | a0003c0002t0007g0034a0003c0002t0007g0035 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.482+12847A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828902 | ||||||
chr5:56828967
|
G | C | 42 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(39): Show | 46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.482+12912G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828967 | ||||||
chr5:56829287
|
A | G | 1 | a0001c0001t0010g0336 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.482+13232A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56829287 | ||||||
chr5:56829349
|
A | AT | 149 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(146): Show | 163 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.482+13313dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56829349 | |||||
chr5:56829349
|
A | ATT | 8 | a0001c0001t0002g0221a0001c0001t0002g0268a0001c0001t0002g0315others(5): Show | 8 | HG02056.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.482+13312_482+1331 others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56829349 | |||||
chr5:56829437
|
C | T | 1 | a0002c0003t0001g0110 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.482+13382C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56829437 | ||||||
chr5:56829526
|
A | G | 81 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(78): Show | 89 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.482+13471A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56829526 | ||||||
chr5:56829529
|
A | T | 1 | a0003c0002t0011g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.482+13474A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56829529 | ||||||
chr5:56829662
|
T | C | 2 | a0002c0003t0007g0055a0002c0003t0013g0054 | 2 | HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.482+13607T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56829662 | ||||||
chr5:56829698
|
G | A | 1 | a0001c0001t0010g0329 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.482+13643G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56829698 | ||||||
chr5:56829869
|
T | A | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.482+13814T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56829869 | ||||||
chr5:56830077
|
T | C | 86 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(83): Show | 94 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.482+14022T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56830077 | ||||||
chr5:56830101
|
G | T | 5 | a0001c0005t0014g0321a0001c0005t0014g0322a0001c0005t0014g0323others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.482+14046G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56830101 | ||||||
chr5:56830164
|
A | G | 2 | a0001c0001t0008g0314a0001c0001t0016g0313 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.482+14109A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56830164 | ||||||
chr5:56830813
|
A | G | 4 | a0002c0004t0001g0107a0002c0004t0001g0108a0002c0004t0001g0109others(1): Show | 4 | HG00621.hp2 NA18947.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+14758A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56830813 | ||||||
chr5:56830885
|
G | GT | 11 | a0003c0002t0004g0038a0003c0002t0005g0037a0003c0002t0007g0012others(8): Show | 12 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.482+14840dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56830885 | |||||
chr5:56830885
|
G | T | 2 | a0003c0002t0001g0030a0003c0002t0001g0031 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.482+14830G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56830885 | ||||||
chr5:56830916
|
A | AT | 64 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(61): Show | 70 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.482+14873dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56830916 | |||||
chr5:56830964
|
A | G | 3 | a0003c0002t0004g0038a0003c0002t0005g0037a0003c0002t0009g0036 | 3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+14909A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56830964 | ||||||
chr5:56831003
|
C | T | 1 | a0010c0020t0018g0131 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.482+14948C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831003 | ||||||
chr5:56831013
|
A | G | 59 | a0001c0001t0028g0312a0002c0004t0005g0106a0003c0002t0001g0171others(56): Show | 65 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.482+14958A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831013 | ||||||
chr5:56831107
|
T | C | 5 | a0003c0002t0017g0215a0003c0009t0015g0028a0003c0009t0019g0326others(2): Show | 5 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.482+15052T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831107 | ||||||
chr5:56831184
|
G | GT | 6 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0001g0112others(3): Show | 6 | HG02622.hp1 HG04115.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.482+15147dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56831184 | |||||
chr5:56831184
|
GT | G | 121 | a0001c0001t0002g0316a0001c0001t0009g0335a0001c0001t0010g0029others(118): Show | 132 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.482+15147delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56831184 | |||||
chr5:56831184
|
GTT | G | 96 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(93): Show | 106 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.482+15146_482+1514 others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56831184 | |||||
chr5:56831286
|
A | G | 2 | a0001c0001t0002g0264a0003c0002t0003g0196 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.482+15231A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831286 | ||||||
chr5:56831403
|
C | G | 1 | a0001c0001t0002g0310 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.482+15348C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831403 | ||||||
chr5:56831458
|
C | T | 1 | a0001c0001t0002g0309 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.482+15403C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831458 | ||||||
chr5:56831734
|
C | T | 9 | a0001c0008t0009g0208a0001c0008t0009g0209a0001c0008t0009g0210others(6): Show | 9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+15679C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831734 | ||||||
chr5:56831852
|
C | G | 1 | a0001c0001t0002g0010 | 3 | HG01952.hp2 NA20300.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.482+15797C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831852 | ||||||
chr5:56831971
|
T | C | 3 | a0003c0002t0004g0038a0003c0002t0005g0037a0003c0002t0009g0036 | 3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+15916T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831971 | ||||||
chr5:56832039
|
G | A | 59 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(56): Show | 66 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.482+15984G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832039 | ||||||
chr5:56832214
|
A | C | 2 | a0002c0003t0001g0100a0002c0003t0006g0101 | 2 | NA18965.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.482+16159A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832214 | ||||||
chr5:56832258
|
G | T | 2 | a0003c0002t0001g0030a0003c0002t0001g0031 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.482+16203G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832258 | ||||||
chr5:56832314
|
A | G | 3 | a0001c0001t0002g0214a0001c0001t0002g0266a0001c0001t0002g0308 | 3 | HG00639.hp2 HG01175.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.482+16259A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832314 | ||||||
chr5:56832320
|
G | A | 6 | a0003c0002t0007g0012a0003c0002t0007g0039a0003c0002t0007g0040others(3): Show | 7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+16265G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832320 | ||||||
chr5:56832578
|
T | C | 1 | a0003c0002t0003g0185 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.482+16523T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832578 | ||||||
chr5:56832628
|
G | A | 1 | a0002c0003t0001g0046 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.482+16573G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832628 | ||||||
chr5:56832714
|
G | T | 5 | a0001c0005t0014g0321a0001c0005t0014g0322a0001c0005t0014g0323others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.482+16659G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832714 | ||||||
chr5:56832903
|
C | T | 10 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0007g0012others(7): Show | 11 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.482+16848C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832903 | ||||||
chr5:56833021
|
A | G | 59 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(56): Show | 65 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.482+16966A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833021 | ||||||
chr5:56833070
|
C | T | 1 | a0001c0005t0004g0234 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.482+17015C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833070 | ||||||
chr5:56833093
|
A | T | 1 | a0011c0017t0002g0311 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.482+17038A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833093 | ||||||
chr5:56833112
|
C | T | 42 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(39): Show | 46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.482+17057C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833112 | ||||||
chr5:56833149
|
C | T | 2 | a0001c0001t0002g0220a0001c0001t0002g0221 | 2 | HG01109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.482+17094C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833149 | ||||||
chr5:56833172
|
G | C | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.482+17117G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833172 | ||||||
chr5:56833224
|
C | T | 2 | a0003c0002t0003g0178a0003c0002t0003g0179 | 2 | NA18977.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.482+17169C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833224 | ||||||
chr5:56833270
|
G | A | 4 | a0002c0003t0001g0059a0002c0003t0001g0061a0002c0003t0001g0112others(1): Show | 4 | HG00642.hp1 HG01346.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+17215G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833270 | ||||||
chr5:56833333
|
G | A | 1 | a0002c0004t0001g0062 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.482+17278G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833333 | ||||||
chr5:56833358
|
A | G | 3 | a0003c0002t0004g0038a0003c0002t0005g0037a0003c0002t0009g0036 | 3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+17303A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833358 | ||||||
chr5:56833499
|
A | G | 4 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0001t0002g0307others(1): Show | 4 | HG00735.hp2 HG01516.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+17444A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833499 | ||||||
chr5:56833507
|
A | G | 1 | a0001c0001t0008g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.482+17452A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833507 | ||||||
chr5:56833533
|
C | T | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.482+17478C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833533 | ||||||
chr5:56833869
|
T | G | 1 | a0001c0001t0002g0315 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.482+17814T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833869 | ||||||
chr5:56833942
|
G | A | 1 | a0001c0008t0009g0208 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.482+17887G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833942 | ||||||
chr5:56833976
|
T | A | 59 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(56): Show | 65 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.482+17921T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833976 | ||||||
chr5:56834139
|
G | GTAA | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.482+18086_482+1808 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56834139 | |||||
chr5:56834150
|
C | A | 1 | a0001c0001t0002g0269 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.482+18095C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56834150 | ||||||
chr5:56834311
|
G | C | 1 | a0001c0001t0002g0309 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.482+18256G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56834311 | ||||||
chr5:56834413
|
A | G | 1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.482+18358A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56834413 | ||||||
chr5:56834436
|
G | A | 1 | a0003c0002t0003g0157 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.482+18381G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56834436 | ||||||
chr5:56834495
|
T | C | 269 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(266): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.482+18440T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56834495 | ||||||
chr5:56834707
|
T | G | 42 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(39): Show | 46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.482+18652T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56834707 | ||||||
chr5:56834713
|
CAAA | C | 4 | a0001c0005t0014g0322a0001c0005t0014g0323a0001c0005t0014g0324others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+18659_482+1866 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56834713 | ||||||
chr5:56834844
|
A | ATTT | 5 | a0001c0005t0014g0321a0001c0005t0014g0322a0001c0005t0014g0323others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.482+18791_482+1879 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56834844 | |||||
chr5:56834856
|
T | C | 14 | a0001c0001t0002g0024a0001c0001t0002g0270a0001c0001t0002g0271others(11): Show | 15 | HG00438.hp1 HG01175.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.482+18801T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56834856 | ||||||
chr5:56835097
|
T | G | 20 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(17): Show | 21 | HG00673.hp2 HG02080.hp1 HG02698.hp2 others(18): Show |
intron_variant | MODIFIER | c.482+19042T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835097 | ||||||
chr5:56835284
|
A | AGACAGGA others(59): Show |
2 | a0002c0003t0006g0136a0002c0003t0030g0126 | 2 | NA18942.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.482+19344_482+1940 others(70): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835284 | |||||
chr5:56835284
|
AGACAGGA others(59): Show |
A | 202 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(199): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.482+19344_482+1940 others(70): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835284 | |||||
chr5:56835289
|
G | A | 1 | a0001c0001t0017g0328 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.482+19234G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835289 | ||||||
chr5:56835306
|
AGACAGGA others(37): Show |
A | 1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.482+19278_482+1932 others(48): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835306 | |||||
chr5:56835319
|
G | A | 1 | a0002c0003t0006g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19264G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835319 | ||||||
chr5:56835323
|
A | G | 1 | a0002c0003t0006g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19268A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835323 | ||||||
chr5:56835324
|
G | C | 1 | a0002c0003t0006g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19269G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835324 | ||||||
chr5:56835325
|
A | C | 1 | a0002c0003t0006g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19270A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835325 | ||||||
chr5:56835326
|
G | T | 1 | a0002c0003t0006g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19271G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835326 | ||||||
chr5:56835331
|
CAAGGAGG others(56): Show |
C | 1 | a0003c0002t0003g0198 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.482+19277_482+1933 others(67): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835331 | ||||||
chr5:56835332
|
A | C | 1 | a0002c0003t0006g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19277A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835332 | ||||||
chr5:56835336
|
A | C | 1 | a0002c0003t0006g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19281A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835336 | ||||||
chr5:56835337
|
G | T | 1 | a0002c0003t0006g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19282G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835337 | ||||||
chr5:56835345
|
A | T | 1 | a0002c0003t0006g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19290A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835345 | ||||||
chr5:56835346
|
G | T | 1 | a0002c0003t0006g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19291G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835346 | ||||||
chr5:56835349
|
T | G | 1 | a0002c0003t0006g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19294T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835349 | ||||||
chr5:56835350
|
T | A | 1 | a0002c0003t0006g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19295T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835350 | ||||||
chr5:56835350
|
TGACAGGA others(81): Show |
T | 11 | a0001c0001t0002g0269a0001c0001t0009g0335a0001c0001t0010g0029others(8): Show | 12 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.482+19328_482+1941 others(92): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835350 | |||||
chr5:56835357
|
AAGGCAGG others(37): Show |
A | 2 | a0003c0002t0004g0038a0003c0002t0005g0037 | 2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+19316_482+1935 others(48): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835357 | |||||
chr5:56835372
|
A | AGACAGGA others(15): Show |
2 | a0001c0001t0002g0218a0001c0001t0008g0217 | 2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.482+19337_482+1933 others(26): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835372 | |||||
chr5:56835372
|
AGACAGGA others(37): Show |
A | 1 | a0001c0001t0028g0312 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.482+19344_482+1938 others(48): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835372 | |||||
chr5:56835393
|
G | T | 10 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0007g0012others(7): Show | 11 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.482+19338G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835393 | ||||||
chr5:56835394
|
A | T | 10 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0007g0012others(7): Show | 11 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.482+19339A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835394 | ||||||
chr5:56835394
|
AGACAAGG others(15): Show |
A | 1 | a0001c0001t0016g0313 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.482+19344_482+1936 others(26): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835394 | |||||
chr5:56835399
|
A | G | 12 | a0001c0001t0002g0218a0001c0001t0008g0217a0003c0002t0001g0030others(9): Show | 13 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.482+19344A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835399 | ||||||
chr5:56835401
|
G | A | 12 | a0001c0001t0002g0218a0001c0001t0008g0217a0003c0002t0001g0030others(9): Show | 13 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.482+19346G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835401 | ||||||
chr5:56835413
|
A | G | 5 | a0001c0005t0004g0231a0001c0005t0004g0232a0001c0005t0004g0236others(2): Show | 5 | HG03831.hp2 NA18960.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.482+19358A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835413 | ||||||
chr5:56835416
|
TGACAGGA others(15): Show |
T | 1 | a0002c0004t0004g0122 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.482+19394_482+1941 others(26): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835416 | |||||
chr5:56835523
|
G | T | 59 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(56): Show | 66 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.482+19468G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835523 | ||||||
chr5:56835594
|
A | G | 337 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(334): Show | 372 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.482+19539A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835594 | ||||||
chr5:56835608
|
T | A | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.482+19553T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835608 | ||||||
chr5:56835702
|
G | C | 1 | a0003c0002t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.482+19647G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835702 | ||||||
chr5:56835725
|
G | A | 1 | a0003c0002t0001g0031 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.482+19670G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835725 | ||||||
chr5:56835978
|
T | A | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.482+19923T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835978 | ||||||
chr5:56836288
|
C | G | 99 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(96): Show | 108 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.482+20233C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56836288 | ||||||
chr5:56836327
|
A | AG | 269 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(266): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.482+20272_483-2027 others(5): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56836327 | ||||||
chr5:56836353
|
G | A | 1 | a0011c0017t0002g0311 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.483-20247G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56836353 | ||||||
chr5:56836621
|
G | A | 1 | a0003c0002t0009g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.483-19979G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56836621 | ||||||
chr5:56836629
|
G | C | 1 | a0002c0003t0001g0059 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.483-19971G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56836629 | ||||||
chr5:56836800
|
T | C | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.483-19800T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56836800 | ||||||
chr5:56837039
|
A | G | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-19561A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56837039 | ||||||
chr5:56837049
|
C | G | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-19551C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56837049 | ||||||
chr5:56837212
|
A | G | 1 | a0001c0001t0002g0304 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.483-19388A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56837212 | ||||||
chr5:56837391
|
T | C | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-19209T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56837391 | ||||||
chr5:56837728
|
G | A | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.483-18872G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56837728 | ||||||
chr5:56837786
|
C | T | 1 | a0001c0011t0009g0204 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.483-18814C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56837786 | ||||||
chr5:56837921
|
G | C | 87 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(84): Show | 95 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.483-18679G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56837921 | ||||||
chr5:56837934
|
G | A | 1 | a0002c0003t0023g0120 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.483-18666G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56837934 | ||||||
chr5:56838040
|
T | G | 2 | a0003c0002t0003g0183a0003c0002t0017g0215 | 2 | NA18986.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.483-18560T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838040 | ||||||
chr5:56838127
|
G | C | 1 | a0003c0002t0003g0181 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.483-18473G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838127 | ||||||
chr5:56838243
|
T | TTC | 222 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(219): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.483-18356_483-1835 others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56838243 | |||||
chr5:56838317
|
A | G | 6 | a0003c0002t0007g0012a0003c0002t0007g0039a0003c0002t0007g0040others(3): Show | 7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.483-18283A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838317 | ||||||
chr5:56838342
|
A | C | 3 | a0001c0001t0002g0219a0001c0001t0002g0220a0001c0001t0002g0221 | 3 | HG01109.hp1 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.483-18258A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838342 | ||||||
chr5:56838380
|
A | G | 2 | a0003c0002t0004g0038a0003c0002t0005g0037 | 2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.483-18220A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838380 | ||||||
chr5:56838449
|
A | G | 42 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(39): Show | 46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.483-18151A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838449 | ||||||
chr5:56838476
|
T | A | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-18124T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838476 | ||||||
chr5:56838539
|
G | A | 1 | a0001c0005t0014g0321 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.483-18061G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838539 | ||||||
chr5:56838733
|
T | G | 22 | a0001c0006t0001g0245a0001c0006t0004g0023a0001c0006t0004g0241others(19): Show | 25 | HG00423.hp2 HG01261.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.483-17867T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838733 | ||||||
chr5:56838895
|
T | TTTTTG | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-17689_483-1768 others(9): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56838895 | |||||
chr5:56838943
|
T | C | 2 | a0001c0001t0002g0220a0001c0001t0002g0221 | 2 | HG01109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.483-17657T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838943 | ||||||
chr5:56838995
|
C | A | 3 | a0001c0001t0002g0219a0001c0001t0002g0220a0001c0001t0002g0221 | 3 | HG01109.hp1 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.483-17605C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838995 | ||||||
chr5:56839008
|
G | A | 1 | a0001c0006t0004g0241 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.483-17592G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839008 | ||||||
chr5:56839037
|
T | C | 1 | a0004c0012t0008g0056 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.483-17563T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839037 | ||||||
chr5:56839072
|
G | C | 1 | a0002c0003t0001g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.483-17528G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839072 | ||||||
chr5:56839099
|
G | C | 1 | a0002c0003t0018g0086 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.483-17501G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839099 | ||||||
chr5:56839219
|
C | T | 1 | a0011c0017t0002g0311 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.483-17381C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839219 | ||||||
chr5:56839238
|
T | C | 4 | a0004c0012t0008g0056a0004c0012t0008g0058a0004c0012t0016g0057others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-17362T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839238 | ||||||
chr5:56839429
|
T | A | 1 | a0002c0007t0001g0087 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.483-17171T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839429 | ||||||
chr5:56839627
|
A | G | 2 | a0002c0003t0001g0018a0002c0003t0001g0145 | 3 | HG02486.hp2 HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.483-16973A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839627 | ||||||
chr5:56839719
|
T | C | 3 | a0002c0003t0013g0088a0002c0003t0013g0089a0002c0003t0013g0125 | 3 | HG02976.hp1 HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.483-16881T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839719 | ||||||
chr5:56839750
|
A | G | 2 | a0003c0002t0004g0038a0003c0002t0005g0037 | 2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.483-16850A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839750 | ||||||
chr5:56839815
|
A | C | 1 | a0002c0003t0001g0110 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.483-16785A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839815 | ||||||
chr5:56839904
|
C | CTTG | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.483-16694_483-1669 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56839904 | |||||
chr5:56839978
|
C | T | 2 | a0001c0001t0002g0220a0001c0001t0002g0221 | 2 | HG01109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.483-16622C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839978 | ||||||
chr5:56839989
|
G | T | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-16611G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839989 | ||||||
chr5:56839998
|
T | A | 1 | a0002c0003t0001g0111 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.483-16602T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839998 | ||||||
chr5:56840246
|
C | G | 1 | a0001c0001t0002g0303 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.483-16354C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840246 | ||||||
chr5:56840408
|
A | G | 87 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(84): Show | 95 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.483-16192A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840408 | ||||||
chr5:56840448
|
AAAT | A | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-16148_483-1614 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56840448 | |||||
chr5:56840513
|
C | T | 1 | a0003c0002t0003g0191 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.483-16087C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840513 | ||||||
chr5:56840516
|
G | T | 222 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(219): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.483-16084G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840516 | ||||||
chr5:56840588
|
C | A | 1 | a0001c0006t0004g0241 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.483-16012C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840588 | ||||||
chr5:56840665
|
A | G | 87 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(84): Show | 95 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.483-15935A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840665 | ||||||
chr5:56840737
|
C | G | 1 | a0003c0002t0003g0150 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.483-15863C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840737 | ||||||
chr5:56840741
|
T | C | 3 | a0003c0002t0004g0038a0003c0002t0005g0037a0003c0002t0009g0036 | 3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.483-15859T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840741 | ||||||
chr5:56840776
|
C | G | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-15824C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840776 | ||||||
chr5:56840870
|
G | GT | 68 | a0001c0001t0002g0024a0001c0001t0002g0303a0001c0006t0004g0251others(65): Show | 75 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.483-15712dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56840870 | |||||
chr5:56840870
|
GT | G | 19 | a0001c0001t0016g0275a0001c0006t0004g0260a0001c0008t0009g0208others(16): Show | 19 | HG01081.hp2 HG01496.hp1 HG02717.hp1 others(16): Show |
intron_variant | MODIFIER | c.483-15712delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56840870 | |||||
chr5:56841025
|
A | G | 1 | a0001c0001t0002g0303 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.483-15575A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841025 | ||||||
chr5:56841201
|
T | TAA | 6 | a0001c0001t0002g0263a0001c0001t0002g0276a0001c0001t0002g0277others(3): Show | 6 | HG02683.hp2 HG03654.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.483-15399_483-1539 others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841201 | ||||||
chr5:56841202
|
T | A | 7 | a0001c0001t0002g0263a0001c0001t0002g0276a0001c0001t0002g0277others(4): Show | 7 | HG02683.hp2 HG03654.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.483-15398T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841202 | ||||||
chr5:56841202
|
T | TA | 39 | a0001c0001t0002g0219a0001c0001t0002g0220a0001c0001t0002g0221others(36): Show | 42 | HG00423.hp2 HG01109.hp1 HG01256.hp2 others(39): Show |
intron_variant | MODIFIER | c.483-15384dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56841202 | |||||
chr5:56841202
|
T | TAA | 65 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(62): Show | 73 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.483-15385_483-1538 others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56841202 | |||||
chr5:56841202
|
TA | T | 43 | a0001c0005t0004g0238a0002c0004t0001g0006a0002c0004t0001g0013others(40): Show | 49 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.483-15384delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56841202 | |||||
chr5:56841273
|
T | G | 1 | a0002c0004t0001g0066 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.483-15327T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841273 | ||||||
chr5:56841278
|
C | T | 5 | a0001c0005t0014g0321a0001c0005t0014g0322a0001c0005t0014g0323others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.483-15322C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841278 | ||||||
chr5:56841343
|
G | C | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.483-15257G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841343 | ||||||
chr5:56841386
|
T | C | 2 | a0001c0005t0004g0231a0001c0005t0004g0232 | 2 | NA18960.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.483-15214T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841386 | ||||||
chr5:56841407
|
C | T | 1 | a0001c0006t0004g0250 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.483-15193C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841407 | ||||||
chr5:56841408
|
G | C | 1 | a0003c0002t0003g0160 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.483-15192G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841408 | ||||||
chr5:56841427
|
A | G | 9 | a0001c0008t0009g0208a0001c0008t0009g0209a0001c0008t0009g0210others(6): Show | 9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.483-15173A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841427 | ||||||
chr5:56841487
|
T | C | 1 | a0001c0001t0002g0270 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.483-15113T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841487 | ||||||
chr5:56841541
|
GGATTATA others(4): Show |
G | 1 | a0003c0002t0003g0157 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.483-15056_483-1504 others(15): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56841541 | |||||
chr5:56841605
|
C | T | 61 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(58): Show | 68 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.483-14995C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841605 | ||||||
chr5:56841626
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.483-14974C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841626 | ||||||
chr5:56841630
|
T | C | 3 | a0002c0003t0001g0052a0002c0003t0001g0091a0002c0003t0001g0092 | 3 | HG02559.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.483-14970T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841630 | ||||||
chr5:56841960
|
G | A | 222 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(219): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.483-14640G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841960 | ||||||
chr5:56842009
|
C | T | 1 | a0002c0004t0001g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.483-14591C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56842009 | ||||||
chr5:56842261
|
A | G | 1 | a0001c0001t0002g0265 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.483-14339A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56842261 | ||||||
chr5:56842507
|
C | T | 1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.483-14093C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56842507 | ||||||
chr5:56842650
|
T | C | 1 | a0001c0001t0010g0029 | 2 | HG02572.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.483-13950T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56842650 | ||||||
chr5:56842655
|
C | T | 10 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0007g0012others(7): Show | 11 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.483-13945C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56842655 | ||||||
chr5:56842951
|
C | T | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-13649C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56842951 | ||||||
chr5:56843147
|
G | T | 1 | a0003c0002t0003g0177 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.483-13453G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843147 | ||||||
chr5:56843255
|
C | T | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-13345C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843255 | ||||||
chr5:56843355
|
C | G | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-13245C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843355 | ||||||
chr5:56843366
|
A | T | 1 | a0003c0002t0003g0188 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.483-13234A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843366 | ||||||
chr5:56843373
|
T | C | 1 | a0002c0003t0013g0054 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.483-13227T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843373 | ||||||
chr5:56843419
|
T | C | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-13181T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843419 | ||||||
chr5:56843444
|
C | T | 1 | a0003c0009t0019g0327 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.483-13156C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843444 | ||||||
chr5:56843482
|
A | T | 2 | a0003c0002t0007g0034a0003c0002t0007g0035 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.483-13118A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843482 | ||||||
chr5:56843507
|
G | C | 1 | a0001c0001t0002g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.483-13093G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843507 | ||||||
chr5:56843512
|
A | G | 1 | a0002c0003t0001g0046 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.483-13088A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843512 | ||||||
chr5:56843717
|
G | A | 9 | a0001c0008t0009g0208a0001c0008t0009g0209a0001c0008t0009g0210others(6): Show | 9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.483-12883G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843717 | ||||||
chr5:56843746
|
T | C | 1 | a0001c0001t0008g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.483-12854T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843746 | ||||||
chr5:56843930
|
C | G | 1 | a0002c0003t0013g0089 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.483-12670C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843930 | ||||||
chr5:56843963
|
C | T | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-12637C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843963 | ||||||
chr5:56844082
|
T | C | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-12518T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844082 | ||||||
chr5:56844094
|
A | G | 2 | a0003c0002t0007g0034a0003c0002t0007g0035 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.483-12506A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844094 | ||||||
chr5:56844177
|
T | A | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-12423T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844177 | ||||||
chr5:56844182
|
G | GT | 2 | a0001c0006t0004g0023a0001c0006t0004g0254 | 3 | HG01516.hp1 HG01517.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.483-12418_483-1241 others(5): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844182 | ||||||
chr5:56844183
|
G | GT | 115 | a0001c0001t0002g0025a0001c0001t0002g0219a0001c0001t0002g0221others(112): Show | 129 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.483-12393dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56844183 | |||||
chr5:56844183
|
G | GTT | 68 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0026others(65): Show | 75 | HG00099.hp2 HG00639.hp2 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.483-12394_483-1239 others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56844183 | |||||
chr5:56844183
|
G | GTTT | 20 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0213others(17): Show | 22 | HG00438.hp1 HG00642.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.483-12395_483-1239 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56844183 | |||||
chr5:56844183
|
G | T | 9 | a0001c0006t0004g0023a0001c0006t0004g0249a0001c0006t0004g0254others(6): Show | 10 | HG01243.hp2 HG01361.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.483-12417G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844183 | ||||||
chr5:56844183
|
GT | G | 10 | a0001c0008t0009g0209a0001c0008t0009g0210a0001c0008t0009g0212others(7): Show | 10 | HG01081.hp2 HG01169.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.483-12393delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56844183 | |||||
chr5:56844183
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0008g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.483-12407_483-1239 others(19): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56844183 | |||||
chr5:56844229
|
G | A | 1 | a0003c0002t0009g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.483-12371G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844229 | ||||||
chr5:56844304
|
C | T | 2 | a0003c0002t0009g0036a0003c0002t0017g0215 | 2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.483-12296C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844304 | ||||||
chr5:56844336
|
T | C | 1 | a0002c0004t0001g0044 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.483-12264T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844336 | ||||||
chr5:56844374
|
T | C | 270 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(267): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.483-12226T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844374 | ||||||
chr5:56844383
|
G | C | 1 | a0002c0003t0013g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.483-12217G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844383 | ||||||
chr5:56844415
|
G | A | 1 | a0001c0005t0014g0322 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.483-12185G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844415 | ||||||
chr5:56844422
|
G | A | 1 | a0001c0001t0028g0312 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.483-12178G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844422 | ||||||
chr5:56844430
|
T | C | 1 | a0001c0001t0028g0312 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.483-12170T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844430 | ||||||
chr5:56844452
|
T | G | 1 | a0003c0002t0012g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.483-12148T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844452 | ||||||
chr5:56844458
|
T | C | 1 | a0003c0002t0003g0161 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.483-12142T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844458 | ||||||
chr5:56844460
|
T | A | 1 | a0002c0004t0001g0062 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.483-12140T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844460 | ||||||
chr5:56844511
|
G | C | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.483-12089G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844511 | ||||||
chr5:56844599
|
T | C | 1 | a0003c0002t0004g0038 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.483-12001T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844599 | ||||||
chr5:56844641
|
C | T | 1 | a0003c0002t0012g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.483-11959C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844641 | ||||||
chr5:56844646
|
G | A | 1 | a0010c0020t0018g0131 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.483-11954G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844646 | ||||||
chr5:56844831
|
C | T | 3 | a0001c0001t0002g0310a0001c0001t0008g0274a0001c0001t0026g0272 | 3 | HG00438.hp1 NA18960.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.483-11769C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844831 | ||||||
chr5:56844859
|
AAAG | A | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-11735_483-1173 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56844859 | |||||
chr5:56844900
|
A | G | 42 | a0002c0004t0001g0006a0002c0004t0001g0013a0002c0004t0001g0044others(39): Show | 48 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.483-11700A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844900 | ||||||
chr5:56844991
|
C | T | 1 | a0001c0001t0002g0309 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.483-11609C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844991 | ||||||
chr5:56845076
|
T | G | 1 | a0001c0001t0002g0318 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.483-11524T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845076 | ||||||
chr5:56845126
|
A | G | 3 | a0003c0002t0004g0038a0003c0002t0005g0037a0003c0002t0009g0036 | 3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.483-11474A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845126 | ||||||
chr5:56845206
|
A | G | 2 | a0006c0013t0002g0299a0006c0013t0002g0302 | 2 | HG00642.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.483-11394A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845206 | ||||||
chr5:56845328
|
A | G | 22 | a0001c0006t0001g0245a0001c0006t0004g0023a0001c0006t0004g0241others(19): Show | 25 | HG00423.hp2 HG01261.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.483-11272A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845328 | ||||||
chr5:56845420
|
CA | C | 9 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(6): Show | 10 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.483-11179delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845420 | ||||||
chr5:56845532
|
C | CTCTCTAG others(21): Show |
2 | a0003c0002t0009g0036a0003c0002t0017g0215 | 2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.483-11066_483-1103 others(32): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56845532 | |||||
chr5:56845540
|
G | T | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-11060G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845540 | ||||||
chr5:56845568
|
T | G | 1 | a0002c0004t0001g0078 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.483-11032T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845568 | ||||||
chr5:56845685
|
C | T | 2 | a0003c0002t0001g0030a0003c0002t0001g0031 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.483-10915C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845685 | ||||||
chr5:56845709
|
A | T | 9 | a0001c0008t0009g0208a0001c0008t0009g0209a0001c0008t0009g0210others(6): Show | 9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.483-10891A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845709 | ||||||
chr5:56845802
|
G | A | 1 | a0001c0001t0002g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.483-10798G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845802 | ||||||
chr5:56845843
|
G | A | 1 | a0001c0001t0008g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.483-10757G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845843 | ||||||
chr5:56845950
|
G | C | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.483-10650G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845950 | ||||||
chr5:56845958
|
A | G | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-10642A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845958 | ||||||
chr5:56846100
|
G | A | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.483-10500G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846100 | ||||||
chr5:56846169
|
A | C | 1 | a0003c0002t0012g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.483-10431A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846169 | ||||||
chr5:56846239
|
G | A | 1 | a0003c0002t0009g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.483-10361G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846239 | ||||||
chr5:56846304
|
G | C | 1 | a0001c0001t0002g0024 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.483-10296G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846304 | ||||||
chr5:56846534
|
A | G | 4 | a0003c0002t0003g0159a0003c0002t0003g0170a0003c0002t0003g0175others(1): Show | 4 | NA18975.hp2 NA19056.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-10066A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846534 | ||||||
chr5:56846554
|
A | G | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.483-10046A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846554 | ||||||
chr5:56846610
|
G | A | 1 | a0001c0001t0008g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.483-9990G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846610 | ||||||
chr5:56846720
|
G | C | 222 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(219): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.483-9880G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846720 | ||||||
chr5:56846774
|
G | A | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.483-9826G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846774 | ||||||
chr5:56846816
|
A | C | 4 | a0001c0011t0009g0204a0001c0011t0009g0206a0001c0011t0009g0207others(1): Show | 4 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-9784A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846816 | ||||||
chr5:56846866
|
T | G | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.483-9734T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846866 | ||||||
chr5:56846875
|
C | T | 1 | a0001c0001t0002g0277 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.483-9725C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846875 | ||||||
chr5:56846993
|
CTACATT | C | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-9605_483-9600d others(8): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56846993 | |||||
chr5:56847034
|
A | G | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-9566A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847034 | ||||||
chr5:56847172
|
C | T | 42 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(39): Show | 46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.483-9428C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847172 | ||||||
chr5:56847318
|
C | T | 1 | a0001c0011t0025g0205 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.483-9282C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847318 | ||||||
chr5:56847319
|
G | A | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-9281G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847319 | ||||||
chr5:56847332
|
C | T | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-9268C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847332 | ||||||
chr5:56847390
|
A | C | 42 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(39): Show | 46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.483-9210A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847390 | ||||||
chr5:56847592
|
T | C | 87 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(84): Show | 95 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.483-9008T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847592 | ||||||
chr5:56847609
|
A | G | 1 | a0004c0015t0008g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.483-8991A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847609 | ||||||
chr5:56847964
|
A | G | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-8636A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847964 | ||||||
chr5:56848058
|
A | G | 1 | a0002c0004t0004g0077 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.483-8542A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848058 | ||||||
chr5:56848091
|
G | A | 1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.483-8509G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848091 | ||||||
chr5:56848102
|
C | CA | 148 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(145): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.483-8488dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56848102 | |||||
chr5:56848102
|
C | CAA | 60 | a0001c0006t0004g0241a0003c0002t0001g0171a0003c0002t0001g0174others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-8489_483-8488d others(4): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56848102 | |||||
chr5:56848189
|
T | C | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-8411T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848189 | ||||||
chr5:56848230
|
T | A | 2 | a0001c0001t0002g0267a0001c0001t0002g0289 | 2 | HG01256.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.483-8370T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848230 | ||||||
chr5:56848325
|
G | A | 222 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(219): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.483-8275G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848325 | ||||||
chr5:56848409
|
T | C | 1 | a0003c0002t0012g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.483-8191T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848409 | ||||||
chr5:56848437
|
C | T | 1 | a0002c0004t0005g0076 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.483-8163C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848437 | ||||||
chr5:56848509
|
G | A | 1 | a0001c0001t0002g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.483-8091G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848509 | ||||||
chr5:56848526
|
T | G | 1 | a0003c0002t0003g0033 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.483-8074T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848526 | ||||||
chr5:56848582
|
C | T | 337 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(334): Show | 372 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.483-8018C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848582 | ||||||
chr5:56848701
|
T | G | 1 | a0002c0003t0001g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.483-7899T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848701 | ||||||
chr5:56848775
|
G | A | 1 | a0002c0007t0001g0094 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.483-7825G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848775 | ||||||
chr5:56849104
|
T | C | 1 | a0001c0006t0004g0242 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.483-7496T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849104 | ||||||
chr5:56849230
|
G | T | 162 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(159): Show | 176 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.483-7370G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849230 | ||||||
chr5:56849241
|
T | C | 162 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(159): Show | 176 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.483-7359T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849241 | ||||||
chr5:56849241
|
T | G | 14 | a0003c0002t0003g0185a0003c0002t0003g0186a0003c0002t0003g0187others(11): Show | 14 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.483-7359T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849241 | ||||||
chr5:56849243
|
G | A | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-7357G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849243 | ||||||
chr5:56849326
|
G | A | 2 | a0003c0002t0004g0038a0003c0002t0005g0037 | 2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.483-7274G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849326 | ||||||
chr5:56849353
|
TA | T | 197 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(194): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.483-7230delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56849353 | |||||
chr5:56849355
|
A | T | 72 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(69): Show | 80 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.483-7245A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849355 | ||||||
chr5:56849356
|
A | T | 1 | a0001c0001t0002g0267 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.483-7244A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849356 | ||||||
chr5:56849496
|
A | G | 1 | a0002c0004t0005g0074 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.483-7104A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849496 | ||||||
chr5:56849502
|
T | C | 1 | a0003c0002t0003g0032 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.483-7098T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849502 | ||||||
chr5:56849502
|
T | G | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-7098T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849502 | ||||||
chr5:56849602
|
G | A | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-6998G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849602 | ||||||
chr5:56849719
|
G | A | 1 | a0003c0002t0003g0184 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.483-6881G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849719 | ||||||
chr5:56849754
|
GTTTGGT | G | 73 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(70): Show | 81 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.483-6829_483-6824d others(8): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56849754 | |||||
chr5:56849783
|
G | C | 1 | a0003c0002t0009g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.483-6817G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849783 | ||||||
chr5:56849977
|
A | G | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.483-6623A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849977 | ||||||
chr5:56849985
|
C | T | 2 | a0003c0002t0009g0036a0003c0002t0017g0215 | 2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.483-6615C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849985 | ||||||
chr5:56850038
|
G | A | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-6562G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56850038 | ||||||
chr5:56850069
|
G | A | 2 | a0001c0005t0004g0233a0001c0005t0004g0234 | 2 | HG03239.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.483-6531G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56850069 | ||||||
chr5:56850170
|
G | A | 18 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0027others(15): Show | 24 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.483-6430G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56850170 | ||||||
chr5:56850203
|
T | C | 1 | a0003c0002t0007g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.483-6397T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56850203 | ||||||
chr5:56850301
|
T | A | 1 | a0003c0002t0009g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.483-6299T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56850301 | ||||||
chr5:56850866
|
A | G | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-5734A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56850866 | ||||||
chr5:56850989
|
C | T | 1 | a0002c0003t0005g0060 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.483-5611C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56850989 | ||||||
chr5:56851113
|
AT | A | 96 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(93): Show | 105 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.483-5483delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56851113 | |||||
chr5:56851156
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.483-5444G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56851156 | ||||||
chr5:56851226
|
A | G | 228 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(225): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.483-5374A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56851226 | ||||||
chr5:56851304
|
C | G | 1 | a0003c0002t0009g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.483-5296C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56851304 | ||||||
chr5:56851397
|
C | T | 2 | a0003c0002t0007g0034a0003c0002t0007g0035 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.483-5203C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56851397 | ||||||
chr5:56851595
|
A | G | 2 | a0002c0003t0001g0091a0002c0003t0001g0092 | 2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.483-5005A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56851595 | ||||||
chr5:56851618
|
G | A | 4 | a0001c0011t0009g0204a0001c0011t0009g0206a0001c0011t0009g0207others(1): Show | 4 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-4982G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56851618 | ||||||
chr5:56851768
|
G | A | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-4832G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56851768 | ||||||
chr5:56851937
|
G | A | 1 | a0002c0003t0001g0118 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.483-4663G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56851937 | ||||||
chr5:56852035
|
A | G | 20 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(17): Show | 21 | HG00673.hp2 HG02080.hp1 HG02698.hp2 others(18): Show |
intron_variant | MODIFIER | c.483-4565A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852035 | ||||||
chr5:56852083
|
GA | G | 168 | a0001c0001t0028g0312a0001c0005t0001g0235a0001c0005t0004g0022others(165): Show | 186 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.483-4503delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56852083 | |||||
chr5:56852083
|
GAA | G | 95 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(92): Show | 104 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.483-4504_483-4503d others(4): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56852083 | |||||
chr5:56852085
|
A | G | 1 | a0003c0002t0012g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.483-4515A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852085 | ||||||
chr5:56852086
|
A | G | 1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.483-4514A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852086 | ||||||
chr5:56852113
|
G | A | 3 | a0002c0003t0001g0128a0002c0003t0018g0127a0010c0020t0018g0131 | 3 | HG02015.hp2 HG03669.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.483-4487G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852113 | ||||||
chr5:56852125
|
T | C | 7 | a0002c0004t0001g0045a0002c0004t0001g0062a0002c0004t0001g0064others(4): Show | 7 | NA18957.hp2 NA18959.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.483-4475T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852125 | ||||||
chr5:56852289
|
G | A | 3 | a0001c0001t0002g0213a0001c0001t0002g0279a0001c0001t0008g0300 | 3 | HG00738.hp2 HG01074.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.483-4311G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852289 | ||||||
chr5:56852349
|
C | T | 2 | a0003c0002t0004g0038a0003c0002t0005g0037 | 2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.483-4251C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852349 | ||||||
chr5:56852605
|
T | C | 1 | a0002c0004t0001g0148 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.483-3995T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852605 | ||||||
chr5:56852681
|
G | A | 1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.483-3919G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852681 | ||||||
chr5:56852783
|
C | T | 2 | a0001c0001t0010g0332a0001c0001t0010g0334 | 2 | HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.483-3817C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852783 | ||||||
chr5:56852914
|
C | A | 82 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(79): Show | 90 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.483-3686C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852914 | ||||||
chr5:56853214
|
A | G | 14 | a0001c0005t0014g0321a0001c0005t0014g0322a0001c0005t0014g0323others(11): Show | 14 | HG01081.hp2 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.483-3386A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56853214 | ||||||
chr5:56853329
|
A | G | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-3271A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56853329 | ||||||
chr5:56853405
|
A | G | 1 | a0001c0001t0002g0304 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.483-3195A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56853405 | ||||||
chr5:56853580
|
G | C | 2 | a0003c0002t0009g0036a0003c0002t0017g0215 | 2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.483-3020G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56853580 | ||||||
chr5:56853602
|
T | G | 222 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(219): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.483-2998T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56853602 | ||||||
chr5:56853716
|
T | C | 1 | a0003c0002t0009g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.483-2884T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56853716 | ||||||
chr5:56853984
|
C | T | 1 | a0009c0016t0002g0287 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.483-2616C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56853984 | ||||||
chr5:56854306
|
G | T | 1 | a0001c0001t0002g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.483-2294G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56854306 | ||||||
chr5:56854384
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.483-2216A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56854384 | ||||||
chr5:56854432
|
C | CA | 53 | a0001c0001t0002g0261a0001c0001t0002g0286a0001c0001t0002g0298others(50): Show | 59 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.483-2150dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56854432 | |||||
chr5:56854432
|
C | CAA | 181 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(178): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.483-2151_483-2150d others(4): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56854432 | |||||
chr5:56854432
|
C | CAAA | 24 | a0001c0001t0002g0263a0001c0001t0002g0276a0001c0001t0002g0277others(21): Show | 25 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.483-2152_483-2150d others(5): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56854432 | |||||
chr5:56854447
|
A | G | 1 | a0002c0007t0001g0096 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.483-2153A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56854447 | ||||||
chr5:56854506
|
G | A | 2 | a0003c0002t0003g0011a0003c0002t0003g0032 | 3 | HG00558.hp1 NA18964.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.483-2094G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56854506 | ||||||
chr5:56854710
|
A | G | 267 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(264): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.483-1890A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56854710 | ||||||
chr5:56854765
|
G | A | 1 | a0001c0001t0002g0024 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.483-1835G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56854765 | ||||||
chr5:56854795
|
G | C | 82 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(79): Show | 90 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.483-1805G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56854795 | ||||||
chr5:56854976
|
T | G | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.483-1624T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56854976 | ||||||
chr5:56855133
|
CTCCTTTC others(6): Show |
C | 58 | a0003c0002t0003g0002a0003c0002t0003g0008a0003c0002t0003g0011others(55): Show | 65 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.483-1466_483-1454d others(15): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855133 | ||||||
chr5:56855173
|
C | T | 6 | a0003c0002t0007g0012a0003c0002t0007g0039a0003c0002t0007g0040others(3): Show | 7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.483-1427C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855173 | ||||||
chr5:56855230
|
A | T | 1 | a0002c0003t0006g0130 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.483-1370A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855230 | ||||||
chr5:56855272
|
A | G | 18 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0027others(15): Show | 24 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.483-1328A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855272 | ||||||
chr5:56855535
|
C | T | 1 | a0001c0001t0002g0265 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.483-1065C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855535 | ||||||
chr5:56855685
|
GGTATTTC others(5): Show |
G | 2 | a0002c0003t0007g0055a0002c0003t0013g0054 | 2 | HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.483-904_483-893del others(12): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56855685 | |||||
chr5:56855802
|
C | T | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-798C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855802 | ||||||
chr5:56855848
|
A | G | 1 | a0003c0002t0003g0152 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.483-752A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855848 | ||||||
chr5:56855853
|
A | G | 2 | a0001c0001t0002g0263a0001c0001t0002g0277 | 2 | HG02683.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.483-747A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855853 | ||||||
chr5:56855917
|
G | A | 82 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(79): Show | 90 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.483-683G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855917 | ||||||
chr5:56856271
|
A | G | 1 | a0001c0006t0004g0246 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.483-329A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56856271 | ||||||
chr5:56856466
|
G | A | 1 | a0003c0002t0003g0190 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.483-134G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56856466 | ||||||
chr5:56856583
|
T | G | 1 | a0002c0004t0004g0077 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.483-17T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56856583 | ||||||
chr5:56856589
|
C | A | 162 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(159): Show | 176 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.483-11C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56856589 | ||||||
chr5:56856968
|
G | A | 18 | a0001c0006t0001g0245a0001c0006t0004g0023a0001c0006t0004g0241others(15): Show | 21 | HG00423.hp2 HG01261.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.633+218G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56856968 | ||||||
chr5:56857161
|
A | G | 5 | a0001c0005t0014g0321a0001c0005t0014g0322a0001c0005t0014g0323others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.633+411A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857161 | ||||||
chr5:56857214
|
A | G | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.633+464A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857214 | ||||||
chr5:56857265
|
A | G | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.633+515A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857265 | ||||||
chr5:56857393
|
T | C | 2 | a0003c0002t0007g0034a0003c0002t0007g0035 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.633+643T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857393 | ||||||
chr5:56857539
|
G | T | 5 | a0003c0002t0003g0021a0003c0002t0003g0156a0003c0002t0003g0157others(2): Show | 6 | HG00621.hp1 NA18945.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.633+789G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857539 | ||||||
chr5:56857553
|
C | T | 2 | a0003c0002t0003g0190a0003c0002t0003g0191 | 2 | NA18963.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.633+803C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857553 | ||||||
chr5:56857565
|
T | C | 42 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(39): Show | 46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.633+815T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857565 | ||||||
chr5:56857643
|
T | C | 1 | a0001c0006t0004g0023 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.633+893T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857643 | ||||||
chr5:56857711
|
A | C | 1 | a0002c0004t0001g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.633+961A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857711 | ||||||
chr5:56857944
|
G | T | 4 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0154others(1): Show | 4 | HG02155.hp2 NA18942.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.633+1194G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857944 | ||||||
chr5:56857949
|
G | A | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.633+1199G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857949 | ||||||
chr5:56858020
|
G | C | 14 | a0003c0002t0003g0185a0003c0002t0003g0186a0003c0002t0003g0187others(11): Show | 14 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.633+1270G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858020 | ||||||
chr5:56858072
|
A | G | 1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.633+1322A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858072 | ||||||
chr5:56858294
|
G | C | 9 | a0001c0008t0009g0208a0001c0008t0009g0209a0001c0008t0009g0210others(6): Show | 9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.634-1421G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858294 | ||||||
chr5:56858438
|
G | A | 2 | a0001c0001t0002g0282a0001c0001t0002g0288 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.634-1277G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858438 | ||||||
chr5:56858548
|
G | A | 2 | a0001c0001t0002g0282a0001c0001t0002g0288 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.634-1167G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858548 | ||||||
chr5:56858757
|
T | A | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.634-958T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858757 | ||||||
chr5:56858808
|
G | A | 20 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(17): Show | 21 | HG00673.hp2 HG02080.hp1 HG02698.hp2 others(18): Show |
intron_variant | MODIFIER | c.634-907G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858808 | ||||||
chr5:56858817
|
T | C | 3 | a0001c0005t0004g0225a0001c0005t0004g0226a0001c0005t0004g0229 | 3 | NA18945.hp2 NA18982.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.634-898T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858817 | ||||||
chr5:56858993
|
C | T | 1 | a0001c0006t0004g0023 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.634-722C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858993 | ||||||
chr5:56859065
|
TA | T | 194 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(191): Show | 214 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.634-631delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 56859065 | |||||
chr5:56859065
|
TAA | T | 7 | a0001c0001t0002g0281a0001c0005t0014g0321a0001c0006t0004g0242others(4): Show | 7 | HG01243.hp2 HG02809.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.634-632_634-631del others(2): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 56859065 | |||||
chr5:56859199
|
A | AACAC | 162 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(159): Show | 176 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.634-508_634-505dup others(4): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 56859199 | |||||
chr5:56859199
|
A | AACACAC | 64 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(61): Show | 71 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.634-510_634-505dup others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 56859199 | |||||
chr5:56859422
|
T | C | 1 | a0001c0001t0002g0271 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.634-293T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56859422 | ||||||
chr5:56859455
|
T | A | 1 | a0001c0001t0002g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.634-260T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56859455 | ||||||
chr5:56859924
|
A | G | 2 | a0003c0002t0007g0034a0003c0002t0007g0035 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.834+9A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56859924 | ||||||
chr5:56860132
|
C | T | 1 | a0001c0001t0002g0297 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.834+217C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860132 | ||||||
chr5:56860385
|
A | C | 1 | a0003c0002t0012g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.834+470A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860385 | ||||||
chr5:56860545
|
C | T | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.834+630C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860545 | ||||||
chr5:56860581
|
G | A | 95 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(92): Show | 104 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.834+666G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860581 | ||||||
chr5:56860583
|
T | G | 1 | a0001c0008t0009g0208 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.834+668T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860583 | ||||||
chr5:56860592
|
T | C | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.834+677T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860592 | ||||||
chr5:56860628
|
G | A | 42 | a0002c0004t0001g0006a0002c0004t0001g0013a0002c0004t0001g0044others(39): Show | 48 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.834+713G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860628 | ||||||
chr5:56860650
|
C | T | 1 | a0001c0006t0001g0245 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.834+735C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860650 | ||||||
chr5:56860818
|
A | G | 1 | a0001c0006t0004g0248 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.834+903A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860818 | ||||||
chr5:56860856
|
AAAAAAAA others(1): Show |
A | 51 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(48): Show | 55 | HG00423.hp2 HG00673.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.834+954_834+961del others(8): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56860856 | |||||
chr5:56860871
|
A | G | 1 | a0003c0002t0012g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.834+956A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860871 | ||||||
chr5:56860883
|
T | G | 2 | a0002c0003t0007g0114a0002c0003t0007g0117 | 2 | HG02132.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.834+968T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860883 | ||||||
chr5:56860982
|
T | C | 9 | a0001c0008t0009g0208a0001c0008t0009g0209a0001c0008t0009g0210others(6): Show | 9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.834+1067T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860982 | ||||||
chr5:56860998
|
A | AT | 9 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(6): Show | 10 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.834+1084dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56860998 | |||||
chr5:56861205
|
T | C | 10 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0007g0012others(7): Show | 11 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.834+1290T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861205 | ||||||
chr5:56861374
|
T | C | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.834+1459T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861374 | ||||||
chr5:56861551
|
C | T | 2 | a0003c0002t0007g0034a0003c0002t0007g0035 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.834+1636C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861551 | ||||||
chr5:56861568
|
T | TA | 10 | a0002c0003t0001g0048a0002c0003t0001g0105a0002c0003t0005g0115others(7): Show | 10 | HG01361.hp1 HG02071.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.834+1675dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56861568 | |||||
chr5:56861568
|
TA | T | 9 | a0002c0003t0001g0119a0002c0003t0001g0121a0002c0003t0001g0124others(6): Show | 9 | HG01167.hp2 HG01261.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.834+1675delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56861568 | |||||
chr5:56861569
|
A | T | 1 | a0001c0001t0002g0297 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.834+1654A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861569 | ||||||
chr5:56861586
|
A | AG | 3 | a0003c0002t0003g0032a0003c0002t0003g0156a0003c0002t0003g0188 | 3 | HG02738.hp1 NA18964.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.834+1671_834+1672i others(3): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861586 | ||||||
chr5:56861587
|
A | AG | 47 | a0001c0001t0002g0263a0001c0001t0002g0276a0001c0001t0002g0277others(44): Show | 53 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.834+1672_834+1673i others(3): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861587 | ||||||
chr5:56861587
|
A | G | 18 | a0001c0001t0002g0303a0003c0002t0003g0032a0003c0002t0003g0156others(15): Show | 19 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.834+1672A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861587 | ||||||
chr5:56861588
|
A | AG | 73 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(70): Show | 82 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.834+1673_834+1674i others(3): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861588 | ||||||
chr5:56861588
|
A | AGG | 3 | a0003c0002t0003g0157a0003c0002t0003g0168a0003c0002t0003g0178 | 3 | HG00621.hp1 NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.834+1673_834+1674i others(4): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861588 | ||||||
chr5:56861588
|
A | G | 65 | a0001c0001t0002g0263a0001c0001t0002g0276a0001c0001t0002g0277others(62): Show | 72 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.834+1673A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861588 | ||||||
chr5:56861589
|
A | AG | 55 | a0001c0001t0002g0219a0001c0001t0002g0220a0001c0001t0002g0221others(52): Show | 59 | HG00423.hp2 HG00673.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.834+1674_834+1675i others(3): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861589 | ||||||
chr5:56861589
|
A | AGG | 10 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0268others(7): Show | 10 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.834+1674_834+1675i others(4): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861589 | ||||||
chr5:56861589
|
A | G | 141 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(138): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.834+1674A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861589 | ||||||
chr5:56861590
|
A | AAAGG | 10 | a0003c0002t0001g0030a0003c0002t0004g0038a0003c0002t0005g0037others(7): Show | 11 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.834+1675_834+1676i others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861590 | ||||||
chr5:56861590
|
A | AGG | 6 | a0001c0005t0004g0230a0001c0005t0004g0231a0001c0006t0004g0243others(3): Show | 6 | HG01361.hp2 HG02056.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.834+1678_834+1679d others(4): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56861590 | |||||
chr5:56861590
|
A | G | 207 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(204): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.834+1675A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861590 | ||||||
chr5:56861710
|
GAATCTTA others(17): Show |
G | 1 | a0003c0002t0011g0173 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.834+1796_834+1819d others(26): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861710 | ||||||
chr5:56861726
|
G | C | 1 | a0001c0001t0002g0297 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.834+1811G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861726 | ||||||
chr5:56861780
|
G | A | 4 | a0001c0001t0008g0200a0001c0001t0008g0201a0001c0001t0008g0202others(1): Show | 4 | HG02129.hp1 NA18993.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.834+1865G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861780 | ||||||
chr5:56862086
|
TGGGCAGG others(10): Show |
T | 1 | a0009c0016t0002g0287 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.834+2174_834+2190d others(19): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56862086 | |||||
chr5:56862108
|
G | A | 1 | a0009c0016t0002g0287 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.834+2193G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862108 | ||||||
chr5:56862110
|
T | A | 1 | a0009c0016t0002g0287 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.834+2195T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862110 | ||||||
chr5:56862124
|
T | C | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.834+2209T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862124 | ||||||
chr5:56862232
|
C | G | 1 | a0001c0001t0009g0335 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.834+2317C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862232 | ||||||
chr5:56862267
|
C | T | 1 | a0006c0013t0002g0302 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.834+2352C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862267 | ||||||
chr5:56862324
|
T | A | 1 | a0002c0003t0001g0100 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.834+2409T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862324 | ||||||
chr5:56862628
|
C | T | 2 | a0003c0002t0009g0036a0003c0002t0017g0215 | 2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.835-2106C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862628 | ||||||
chr5:56862668
|
C | T | 1 | a0003c0002t0003g0152 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.835-2066C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862668 | ||||||
chr5:56862788
|
TA | T | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.835-1945delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862788 | ||||||
chr5:56862880
|
A | G | 4 | a0001c0011t0009g0204a0001c0011t0009g0206a0001c0011t0009g0207others(1): Show | 4 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-1854A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862880 | ||||||
chr5:56862901
|
G | C | 1 | a0002c0003t0001g0059 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.835-1833G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862901 | ||||||
chr5:56862914
|
C | T | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.835-1820C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862914 | ||||||
chr5:56862944
|
A | G | 1 | a0002c0004t0004g0122 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.835-1790A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862944 | ||||||
chr5:56862953
|
T | C | 1 | a0005c0010t0004g0259 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.835-1781T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862953 | ||||||
chr5:56863023
|
A | G | 1 | a0002c0007t0001g0087 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.835-1711A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863023 | ||||||
chr5:56863210
|
T | A | 1 | a0003c0002t0011g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.835-1524T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863210 | ||||||
chr5:56863223
|
G | A | 2 | a0001c0005t0004g0233a0001c0005t0004g0234 | 2 | HG03239.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.835-1511G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863223 | ||||||
chr5:56863344
|
A | G | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.835-1390A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863344 | ||||||
chr5:56863353
|
A | C | 1 | a0001c0001t0002g0284 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.835-1381A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863353 | ||||||
chr5:56863429
|
T | A | 1 | a0003c0002t0003g0189 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.835-1305T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863429 | ||||||
chr5:56863491
|
T | G | 1 | a0002c0003t0001g0097 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.835-1243T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863491 | ||||||
chr5:56863593
|
A | G | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.835-1141A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863593 | ||||||
chr5:56863682
|
C | T | 1 | a0003c0002t0003g0189 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.835-1052C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863682 | ||||||
chr5:56863751
|
T | C | 150 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(147): Show | 163 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.835-983T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863751 | ||||||
chr5:56863786
|
A | G | 20 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(17): Show | 21 | HG00673.hp2 HG02080.hp1 HG02698.hp2 others(18): Show |
intron_variant | MODIFIER | c.835-948A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863786 | ||||||
chr5:56863995
|
C | T | 1 | a0003c0002t0007g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.835-739C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863995 | ||||||
chr5:56864055
|
G | A | 22 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0027others(19): Show | 28 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.835-679G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56864055 | ||||||
chr5:56864072
|
A | G | 2 | a0001c0001t0008g0314a0001c0001t0016g0313 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.835-662A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56864072 | ||||||
chr5:56864113
|
A | G | 1 | a0003c0002t0003g0184 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.835-621A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56864113 | ||||||
chr5:56864159
|
G | A | 1 | a0001c0005t0005g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.835-575G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56864159 | ||||||
chr5:56864325
|
G | T | 1 | a0002c0004t0005g0106 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.835-409G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56864325 | ||||||
chr5:56864377
|
TC | T | 4 | a0002c0003t0001g0118a0002c0003t0001g0121a0002c0003t0001g0124others(1): Show | 4 | HG02040.hp1 HG02071.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.835-356delC | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56864377 | ||||||
chr5:56864378
|
C | T | 1 | a0002c0003t0001g0119 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.835-356C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56864378 | ||||||
chr5:56864378
|
CT | C | 214 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(211): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.835-339delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56864378 | |||||
chr5:56864378
|
CTT | C | 6 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0316others(3): Show | 6 | HG00735.hp2 HG01168.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.835-340_835-339del others(2): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56864378 | |||||
chr5:56864446
|
C | T | 1 | a0001c0001t0017g0328 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.835-288C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56864446 | ||||||
chr5:56864714
|
T | TA | 14 | a0001c0005t0014g0321a0001c0005t0014g0322a0001c0005t0014g0323others(11): Show | 14 | HG01081.hp2 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.835-11dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56864714 | |||||
chr5:56865520
|
T | C | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+64T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 5/19 | chr5 | 56865520 | ||||||
chr5:56866148
|
C | T | 82 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(79): Show | 90 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1301+171C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56866148 | ||||||
chr5:56866204
|
G | A | 1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1301+227G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56866204 | ||||||
chr5:56866231
|
A | G | 2 | a0003c0002t0003g0195a0003c0002t0003g0196 | 2 | HG00099.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1301+254A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56866231 | ||||||
chr5:56866323
|
G | A | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1301+346G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56866323 | ||||||
chr5:56866419
|
GTGTA | G | 4 | a0004c0012t0008g0056a0004c0012t0008g0058a0004c0012t0016g0057others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301+454_1301+457d others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 56866419 | |||||
chr5:56866439
|
A | C | 1 | a0001c0005t0005g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1301+462A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56866439 | ||||||
chr5:56866463
|
A | T | 1 | a0001c0001t0002g0284 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1301+486A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56866463 | ||||||
chr5:56867014
|
T | C | 2 | a0003c0002t0007g0034a0003c0002t0007g0035 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1301+1037T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867014 | ||||||
chr5:56867150
|
A | G | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301+1173A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867150 | ||||||
chr5:56867224
|
C | T | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1301+1247C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867224 | ||||||
chr5:56867246
|
T | A | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1301+1269T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867246 | ||||||
chr5:56867333
|
G | A | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1301+1356G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867333 | ||||||
chr5:56867367
|
A | G | 1 | a0002c0003t0001g0059 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1301+1390A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867367 | ||||||
chr5:56867423
|
TA | T | 21 | a0001c0001t0002g0024a0001c0001t0002g0263a0001c0001t0002g0270others(18): Show | 22 | HG00438.hp1 HG01175.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1301+1447delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867423 | ||||||
chr5:56867428
|
C | A | 94 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(91): Show | 103 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1301+1451C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867428 | ||||||
chr5:56867468
|
A | G | 1 | a0002c0004t0001g0064 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1301+1491A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867468 | ||||||
chr5:56867482
|
G | A | 2 | a0003c0002t0007g0034a0003c0002t0007g0035 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1301+1505G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867482 | ||||||
chr5:56867573
|
T | C | 1 | a0003c0002t0009g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1301+1596T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867573 | ||||||
chr5:56867643
|
A | G | 37 | a0002c0003t0001g0003a0002c0003t0001g0015a0002c0003t0001g0049others(34): Show | 41 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1301+1666A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867643 | ||||||
chr5:56867960
|
G | A | 82 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(79): Show | 90 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1301+1983G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867960 | ||||||
chr5:56867986
|
A | G | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1301+2009A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867986 | ||||||
chr5:56868026
|
G | A | 8 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0007g0012others(5): Show | 9 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1301+2049G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868026 | ||||||
chr5:56868251
|
G | C | 4 | a0003c0002t0003g0151a0003c0002t0003g0152a0003c0002t0003g0153others(1): Show | 4 | HG03669.hp1 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301+2274G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868251 | ||||||
chr5:56868325
|
T | TAAAAAAA others(312): Show |
1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1301+2361_1301+236 others(323): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 56868325 | |||||
chr5:56868325
|
TA | T | 3 | a0002c0003t0001g0015a0002c0003t0007g0015a0002c0003t0007g0016 | 4 | HG00423.hp1 NA18612.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301+2356delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 56868325 | |||||
chr5:56868396
|
C | T | 222 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(219): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1301+2419C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868396 | ||||||
chr5:56868446
|
G | A | 7 | a0001c0001t0002g0219a0001c0001t0002g0220a0001c0001t0002g0221others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1301+2469G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868446 | ||||||
chr5:56868530
|
G | A | 1 | a0003c0002t0003g0157 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1301+2553G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868530 | ||||||
chr5:56868560
|
A | G | 2 | a0001c0001t0008g0202a0001c0001t0008g0203 | 2 | NA18993.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1301+2583A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868560 | ||||||
chr5:56868605
|
C | T | 1 | a0001c0008t0009g0208 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1301+2628C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868605 | ||||||
chr5:56868631
|
G | A | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1301+2654G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868631 | ||||||
chr5:56868777
|
T | A | 2 | a0001c0001t0002g0010a0001c0001t0002g0291 | 4 | HG01346.hp2 HG01952.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301+2800T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868777 | ||||||
chr5:56868817
|
G | T | 2 | a0001c0001t0002g0267a0001c0001t0002g0289 | 2 | HG01256.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1301+2840G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868817 | ||||||
chr5:56868858
|
C | T | 1 | a0001c0001t0002g0273 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1301+2881C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868858 | ||||||
chr5:56868877
|
G | C | 9 | a0001c0008t0009g0208a0001c0008t0009g0209a0001c0008t0009g0210others(6): Show | 9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1301+2900G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868877 | ||||||
chr5:56869086
|
C | CA | 11 | a0001c0006t0004g0251a0003c0002t0001g0030a0003c0002t0001g0031others(8): Show | 12 | HG01433.hp1 HG01891.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1302-2812dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 56869086 | |||||
chr5:56869097
|
A | G | 1 | a0003c0002t0003g0166 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1302-2813A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56869097 | ||||||
chr5:56869116
|
A | G | 96 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(93): Show | 104 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1302-2794A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56869116 | ||||||
chr5:56869189
|
T | C | 10 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0007g0012others(7): Show | 11 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302-2721T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56869189 | ||||||
chr5:56869230
|
C | T | 4 | a0001c0001t0002g0262a0001c0005t0004g0225a0001c0005t0004g0226others(1): Show | 4 | HG02055.hp1 NA18945.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302-2680C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56869230 | ||||||
chr5:56869370
|
A | G | 1 | a0003c0002t0003g0177 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1302-2540A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56869370 | ||||||
chr5:56869427
|
A | G | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1302-2483A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56869427 | ||||||
chr5:56869487
|
CA | C | 222 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(219): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1302-2415delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 56869487 | |||||
chr5:56869686
|
T | C | 1 | a0001c0001t0010g0029 | 2 | HG02572.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1302-2224T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56869686 | ||||||
chr5:56869928
|
C | T | 9 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(6): Show | 10 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1302-1982C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56869928 | ||||||
chr5:56870087
|
A | G | 42 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(39): Show | 46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.1302-1823A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870087 | ||||||
chr5:56870187
|
A | G | 4 | a0001c0001t0002g0218a0001c0001t0002g0262a0001c0001t0002g0281others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302-1723A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870187 | ||||||
chr5:56870201
|
A | G | 42 | a0002c0004t0001g0006a0002c0004t0001g0013a0002c0004t0001g0044others(39): Show | 48 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1302-1709A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870201 | ||||||
chr5:56870243
|
G | A | 6 | a0003c0002t0007g0012a0003c0002t0007g0039a0003c0002t0007g0040others(3): Show | 7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302-1667G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870243 | ||||||
chr5:56870277
|
G | A | 5 | a0003c0002t0013g0199a0004c0012t0008g0056a0004c0012t0008g0058others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302-1633G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870277 | ||||||
chr5:56870361
|
A | G | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1302-1549A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870361 | ||||||
chr5:56870367
|
C | T | 64 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(61): Show | 71 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1302-1543C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870367 | ||||||
chr5:56870368
|
G | A | 21 | a0001c0001t0002g0024a0001c0001t0002g0263a0001c0001t0002g0270others(18): Show | 22 | HG00438.hp1 HG01175.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1302-1542G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870368 | ||||||
chr5:56870795
|
G | A | 1 | a0001c0001t0010g0334 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1302-1115G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870795 | ||||||
chr5:56871005
|
A | G | 1 | a0003c0002t0003g0186 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1302-905A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56871005 | ||||||
chr5:56872160
|
A | G | 6 | a0001c0001t0002g0269a0001c0001t0002g0304a0001c0001t0002g0305others(3): Show | 6 | HG00735.hp2 HG01074.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1423+129A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 7/19 | chr5 | 56872160 | ||||||
chr5:56872161
|
A | G | 1 | a0002c0004t0001g0079 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1423+130A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 7/19 | chr5 | 56872161 | ||||||
chr5:56872242
|
G | A | 4 | a0001c0011t0009g0204a0001c0011t0009g0206a0001c0011t0009g0207others(1): Show | 4 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1423+211G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 7/19 | chr5 | 56872242 | ||||||
chr5:56872353
|
A | G | 1 | a0001c0001t0002g0307 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1424-288A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 7/19 | chr5 | 56872353 | ||||||
chr5:56872744
|
G | A | 1 | a0003c0002t0012g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1505+22G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 8/19 | chr5 | 56872744 | ||||||
chr5:56873756
|
C | T | 1 | a0003c0002t0003g0165 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1686+751C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56873756 | ||||||
chr5:56873864
|
TA | T | 9 | a0001c0008t0009g0208a0001c0008t0009g0209a0001c0008t0009g0210others(6): Show | 9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1686+860delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56873864 | ||||||
chr5:56873874
|
A | G | 1 | a0002c0003t0027g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1686+869A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56873874 | ||||||
chr5:56874095
|
C | G | 1 | a0002c0004t0001g0109 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1687-937C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874095 | ||||||
chr5:56874110
|
A | C | 1 | a0002c0004t0001g0109 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1687-922A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874110 | ||||||
chr5:56874229
|
T | G | 5 | a0001c0005t0014g0321a0001c0005t0014g0322a0001c0005t0014g0323others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1687-803T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874229 | ||||||
chr5:56874246
|
T | G | 1 | a0003c0002t0009g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1687-786T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874246 | ||||||
chr5:56874376
|
G | A | 2 | a0002c0004t0015g0067a0002c0004t0015g0083 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1687-656G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874376 | ||||||
chr5:56874473
|
C | T | 1 | a0003c0002t0003g0164 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1687-559C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874473 | ||||||
chr5:56874583
|
A | T | 1 | a0002c0003t0001g0112 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1687-449A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874583 | ||||||
chr5:56874648
|
A | G | 6 | a0003c0002t0007g0012a0003c0002t0007g0039a0003c0002t0007g0040others(3): Show | 7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1687-384A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874648 | ||||||
chr5:56874688
|
A | G | 2 | a0001c0006t0004g0254a0001c0006t0004g0255 | 2 | NA18956.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1687-344A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874688 | ||||||
chr5:56874931
|
G | A | 4 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0001t0002g0307others(1): Show | 4 | HG00735.hp2 HG01516.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1687-101G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874931 | ||||||
chr5:56874986
|
C | G | 43 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(40): Show | 47 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.1687-46C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874986 | ||||||
chr5:56875534
|
T | C | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1965+224T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56875534 | ||||||
chr5:56875564
|
G | T | 37 | a0002c0003t0001g0003a0002c0003t0001g0015a0002c0003t0001g0049others(34): Show | 41 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1965+254G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56875564 | ||||||
chr5:56875694
|
T | TAAAAC | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1965+401_1965+405d others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr5 | 56875694 | |||||
chr5:56876148
|
C | T | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1965+838C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876148 | ||||||
chr5:56876174
|
G | C | 42 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(39): Show | 46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.1965+864G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876174 | ||||||
chr5:56876359
|
T | C | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1965+1049T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876359 | ||||||
chr5:56876377
|
G | C | 4 | a0002c0004t0001g0107a0002c0004t0001g0108a0002c0004t0001g0109others(1): Show | 4 | HG00621.hp2 NA18947.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1965+1067G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876377 | ||||||
chr5:56876447
|
G | A | 4 | a0003c0002t0007g0039a0003c0002t0007g0041a0003c0002t0007g0042others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1965+1137G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876447 | ||||||
chr5:56876475
|
G | C | 1 | a0001c0001t0002g0294 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1965+1165G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876475 | ||||||
chr5:56876760
|
T | G | 4 | a0001c0011t0009g0204a0001c0011t0009g0206a0001c0011t0009g0207others(1): Show | 4 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1965+1450T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876760 | ||||||
chr5:56876819
|
T | C | 96 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(93): Show | 104 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1965+1509T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876819 | ||||||
chr5:56876874
|
C | T | 1 | a0001c0006t0004g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1965+1564C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876874 | ||||||
chr5:56876937
|
G | T | 4 | a0004c0012t0008g0056a0004c0012t0008g0058a0004c0012t0016g0057others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1965+1627G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876937 | ||||||
chr5:56876951
|
G | A | 162 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(159): Show | 176 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.1965+1641G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876951 | ||||||
chr5:56877119
|
C | T | 1 | a0003c0002t0011g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1965+1809C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56877119 | ||||||
chr5:56877343
|
G | A | 1 | a0001c0011t0009g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1966-1637G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56877343 | ||||||
chr5:56877411
|
C | T | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1966-1569C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56877411 | ||||||
chr5:56877413
|
A | C | 1 | a0001c0001t0008g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1966-1567A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56877413 | ||||||
chr5:56877479
|
T | G | 1 | a0001c0005t0014g0322 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1966-1501T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56877479 | ||||||
chr5:56877489
|
T | A | 1 | a0001c0001t0002g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1966-1491T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56877489 | ||||||
chr5:56877519
|
AAT | A | 3 | a0001c0001t0002g0319a0003c0002t0003g0185a0003c0002t0003g0186 | 3 | HG04115.hp2 HG04204.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1966-1460_1966-145 others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56877519 | ||||||
chr5:56877520
|
AT | A | 45 | a0001c0001t0002g0284a0001c0001t0002g0293a0001c0005t0001g0235others(42): Show | 49 | HG00423.hp2 HG00673.hp2 HG01169.hp1 others(46): Show |
intron_variant | MODIFIER | c.1966-1443delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr5 | 56877520 | |||||
chr5:56877520
|
ATT | A | 179 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(176): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1966-1444_1966-144 others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr5 | 56877520 | |||||
chr5:56877627
|
A | G | 1 | a0002c0003t0001g0118 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1966-1353A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56877627 | ||||||
chr5:56878083
|
A | G | 5 | a0001c0001t0008g0217a0004c0012t0008g0056a0004c0012t0008g0058others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1966-897A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878083 | ||||||
chr5:56878107
|
G | A | 1 | a0003c0002t0003g0188 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1966-873G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878107 | ||||||
chr5:56878169
|
A | G | 1 | a0001c0001t0002g0270 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1966-811A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878169 | ||||||
chr5:56878356
|
C | T | 3 | a0001c0001t0002g0214a0001c0001t0002g0266a0001c0001t0002g0308 | 3 | HG00639.hp2 HG01175.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1966-624C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878356 | ||||||
chr5:56878382
|
A | G | 1 | a0003c0002t0012g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1966-598A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878382 | ||||||
chr5:56878416
|
G | A | 1 | a0001c0005t0014g0323 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1966-564G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878416 | ||||||
chr5:56878618
|
C | T | 1 | a0001c0006t0001g0245 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1966-362C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878618 | ||||||
chr5:56878625
|
A | G | 18 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0027others(15): Show | 24 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1966-355A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878625 | ||||||
chr5:56878920
|
G | A | 1 | a0002c0004t0001g0064 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1966-60G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878920 | ||||||
chr5:56879395
|
G | A | 1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2087+294G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879395 | ||||||
chr5:56879399
|
A | G | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.2087+298A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879399 | ||||||
chr5:56879549
|
C | CACTGAAT | 9 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(6): Show | 10 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2087+448_2087+449i others(9): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879549 | ||||||
chr5:56879552
|
A | T | 9 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(6): Show | 10 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2087+451A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879552 | ||||||
chr5:56879557
|
A | G | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2087+456A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879557 | ||||||
chr5:56879565
|
C | CA | 87 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(84): Show | 95 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.2087+470dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr5 | 56879565 | |||||
chr5:56879614
|
C | G | 6 | a0003c0002t0007g0012a0003c0002t0007g0039a0003c0002t0007g0040others(3): Show | 7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2087+513C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879614 | ||||||
chr5:56879739
|
C | G | 82 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(79): Show | 90 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.2087+638C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879739 | ||||||
chr5:56879857
|
A | G | 2 | a0001c0008t0009g0212a0001c0008t0017g0211 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2087+756A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879857 | ||||||
chr5:56879873
|
C | T | 1 | a0002c0003t0007g0055 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2087+772C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879873 | ||||||
chr5:56879935
|
A | G | 1 | a0001c0006t0004g0251 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2088-776A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879935 | ||||||
chr5:56880046
|
T | C | 3 | a0001c0001t0002g0219a0001c0001t0002g0220a0001c0001t0002g0221 | 3 | HG01109.hp1 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2088-665T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56880046 | ||||||
chr5:56880144
|
T | A | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.2088-567T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56880144 | ||||||
chr5:56880163
|
A | G | 1 | a0001c0006t0004g0251 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2088-548A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56880163 | ||||||
chr5:56880479
|
T | C | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2088-232T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56880479 | ||||||
chr5:56880619
|
C | T | 42 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(39): Show | 46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.2088-92C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56880619 | ||||||
chr5:56880664
|
G | T | 1 | a0002c0003t0027g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2088-47G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56880664 | ||||||
chr5:56880667
|
T | G | 1 | a0001c0001t0016g0313 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2088-44T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56880667 | ||||||
chr5:56880815
|
C | T | 1 | a0001c0001t0002g0265 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2179+13C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 12/19 | chr5 | 56880815 | ||||||
chr5:56880871
|
C | T | 1 | a0001c0001t0002g0263 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2179+69C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 12/19 | chr5 | 56880871 | ||||||
chr5:56881321
|
A | G | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2369+49A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 13/19 | chr5 | 56881321 | ||||||
chr5:56881367
|
A | T | 1 | a0001c0001t0002g0285 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2369+95A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 13/19 | chr5 | 56881367 | ||||||
chr5:56881485
|
G | C | 2 | a0003c0009t0015g0028a0003c0009t0024g0028 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2370-85G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 13/19 | chr5 | 56881485 | ||||||
chr5:56881521
|
T | G | 1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2370-49T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 13/19 | chr5 | 56881521 | ||||||
chr5:56881542
|
T | C | 1 | a0002c0004t0001g0078 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2370-28T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 13/19 | chr5 | 56881542 | ||||||
chr5:56882891
|
T | C | 2 | a0001c0001t0002g0267a0001c0001t0002g0289 | 2 | HG01256.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.3666+25T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/19 | chr5 | 56882891 | ||||||
chr5:56883001
|
C | G | 9 | a0001c0008t0009g0208a0001c0008t0009g0209a0001c0008t0009g0210others(6): Show | 9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3666+135C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/19 | chr5 | 56883001 | ||||||
chr5:56883034
|
T | G | 1 | a0001c0008t0017g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3666+168T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/19 | chr5 | 56883034 | ||||||
chr5:56883277
|
A | G | 1 | a0002c0004t0005g0071 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3667-250A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/19 | chr5 | 56883277 | ||||||
chr5:56883385
|
C | T | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.3667-142C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/19 | chr5 | 56883385 | ||||||
chr5:56883486
|
C | G | 1 | a0005c0010t0004g0258 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3667-41C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/19 | chr5 | 56883486 | ||||||
chr5:56883514
|
G | A | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.3667-13G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/19 | chr5 | 56883514 | ||||||
chr5:56883760
|
T | C | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.3819+81T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56883760 | ||||||
chr5:56883812
|
T | C | 1 | a0003c0002t0017g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3819+133T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56883812 | ||||||
chr5:56883916
|
A | G | 1 | a0001c0001t0002g0213 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3819+237A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56883916 | ||||||
chr5:56884146
|
C | A | 3 | a0001c0001t0002g0214a0001c0001t0002g0266a0001c0001t0002g0308 | 3 | HG00639.hp2 HG01175.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.3819+467C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56884146 | ||||||
chr5:56884146
|
C | CA | 4 | a0001c0001t0028g0312a0001c0006t0001g0245a0001c0006t0004g0023others(1): Show | 5 | HG01261.hp1 HG01361.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3819+476dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr5 | 56884146 | |||||
chr5:56884207
|
C | A | 1 | a0001c0001t0002g0269 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3820-457C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56884207 | ||||||
chr5:56884284
|
GTGCGGTG others(6): Show |
G | 1 | a0001c0001t0002g0308 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3820-377_3820-365d others(15): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr5 | 56884284 | |||||
chr5:56884285
|
T | G | 225 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(222): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.3820-379T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56884285 | ||||||
chr5:56884298
|
T | G | 1 | a0001c0001t0002g0308 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3820-366T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56884298 | ||||||
chr5:56884469
|
T | C | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3820-195T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56884469 | ||||||
chr5:56884653
|
A | G | 64 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(61): Show | 71 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.3820-11A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56884653 | ||||||
chr5:56884954
|
A | G | 4 | a0002c0003t0001g0059a0002c0003t0001g0061a0002c0003t0001g0112others(1): Show | 4 | HG00642.hp1 HG01346.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.3982+128A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 16/19 | chr5 | 56884954 | ||||||
chr5:56885090
|
A | G | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.3982+264A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 16/19 | chr5 | 56885090 | ||||||
chr5:56885281
|
T | C | 1 | a0003c0002t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3982+455T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 16/19 | chr5 | 56885281 | ||||||
chr5:56885388
|
GTTC | G | 224 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(221): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.3983-541_3983-539d others(5): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr5 | 56885388 | |||||
chr5:56885542
|
T | G | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.3983-390T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 16/19 | chr5 | 56885542 | ||||||
chr5:56885604
|
T | G | 14 | a0001c0005t0014g0321a0001c0005t0014g0322a0001c0005t0014g0323others(11): Show | 14 | HG01081.hp2 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.3983-328T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 16/19 | chr5 | 56885604 | ||||||
chr5:56886096
|
A | G | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4114+33A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56886096 | ||||||
chr5:56886105
|
T | G | 1 | a0001c0005t0014g0321 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4114+42T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56886105 | ||||||
chr5:56886328
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4114+265C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56886328 | ||||||
chr5:56886529
|
A | G | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.4114+466A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56886529 | ||||||
chr5:56886585
|
A | T | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4114+522A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56886585 | ||||||
chr5:56886642
|
A | G | 1 | a0002c0004t0004g0122 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4114+579A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56886642 | ||||||
chr5:56886762
|
C | T | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.4115-616C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56886762 | ||||||
chr5:56886847
|
T | C | 14 | a0001c0005t0014g0321a0001c0005t0014g0322a0001c0005t0014g0323others(11): Show | 14 | HG01081.hp2 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.4115-531T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56886847 | ||||||
chr5:56887005
|
C | T | 1 | a0002c0004t0005g0076 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.4115-373C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56887005 | ||||||
chr5:56887046
|
A | G | 1 | a0001c0001t0010g0331 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4115-332A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56887046 | ||||||
chr5:56887186
|
G | A | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4115-192G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56887186 | ||||||
chr5:56887578
|
A | G | 1 | a0001c0001t0002g0317 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4257+58A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56887578 | ||||||
chr5:56887715
|
C | T | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.4257+195C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56887715 | ||||||
chr5:56887739
|
G | A | 1 | a0002c0003t0001g0052 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4257+219G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56887739 | ||||||
chr5:56887810
|
G | C | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.4257+290G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56887810 | ||||||
chr5:56887898
|
T | C | 1 | a0001c0006t0005g0253 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4258-328T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56887898 | ||||||
chr5:56887916
|
T | G | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.4258-310T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56887916 | ||||||
chr5:56887970
|
C | T | 1 | a0002c0003t0001g0144 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4258-256C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56887970 | ||||||
chr5:56888102
|
G | A | 1 | a0001c0001t0002g0273 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4258-124G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56888102 | ||||||
chr5:56888114
|
C | G | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.4258-112C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56888114 | ||||||
chr5:56888617
|
T | C | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.4389+260T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56888617 | ||||||
chr5:56888783
|
C | T | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.4389+426C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56888783 | ||||||
chr5:56888793
|
G | A | 5 | a0001c0005t0014g0321a0001c0005t0014g0322a0001c0005t0014g0323others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4389+436G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56888793 | ||||||
chr5:56888986
|
T | G | 1 | a0001c0001t0002g0265 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4389+629T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56888986 | ||||||
chr5:56889099
|
G | C | 42 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(39): Show | 46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.4389+742G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889099 | ||||||
chr5:56889175
|
G | A | 1 | a0008c0019t0005g0069 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.4389+818G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889175 | ||||||
chr5:56889201
|
C | T | 2 | a0003c0002t0009g0036a0003c0002t0017g0215 | 2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4389+844C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889201 | ||||||
chr5:56889210
|
C | T | 1 | a0001c0001t0002g0296 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4389+853C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889210 | ||||||
chr5:56889300
|
C | CT | 59 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(56): Show | 65 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.4389+944dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr5 | 56889300 | |||||
chr5:56889316
|
G | A | 106 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(103): Show | 115 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.4389+959G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889316 | ||||||
chr5:56889334
|
A | G | 1 | a0001c0001t0017g0328 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4389+977A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889334 | ||||||
chr5:56889454
|
T | A | 226 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.4389+1097T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889454 | ||||||
chr5:56889489
|
A | G | 14 | a0001c0005t0014g0321a0001c0005t0014g0322a0001c0005t0014g0323others(11): Show | 14 | HG01081.hp2 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.4389+1132A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889489 | ||||||
chr5:56889969
|
G | A | 1 | a0001c0001t0002g0265 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4389+1612G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889969 | ||||||
chr5:56889978
|
G | A | 4 | a0002c0004t0001g0107a0002c0004t0001g0108a0002c0004t0001g0109others(1): Show | 4 | HG00621.hp2 NA18947.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.4389+1621G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889978 | ||||||
chr5:56890035
|
A | T | 5 | a0001c0008t0009g0208a0001c0008t0009g0209a0001c0008t0009g0210others(2): Show | 5 | HG02809.hp1 HG03225.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.4389+1678A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890035 | ||||||
chr5:56890162
|
C | T | 2 | a0003c0002t0003g0156a0003c0002t0003g0169 | 2 | NA18992.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.4389+1805C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890162 | ||||||
chr5:56890212
|
C | T | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.4389+1855C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890212 | ||||||
chr5:56890435
|
C | G | 2 | a0002c0003t0020g0134a0002c0003t0020g0135 | 2 | HG01928.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.4389+2078C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890435 | ||||||
chr5:56890492
|
G | A | 1 | a0002c0004t0001g0107 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4389+2135G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890492 | ||||||
chr5:56890612
|
G | A | 42 | a0001c0005t0001g0235a0001c0005t0004g0022a0001c0005t0004g0225others(39): Show | 46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.4389+2255G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890612 | ||||||
chr5:56890662
|
C | T | 1 | a0002c0007t0001g0094 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4389+2305C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890662 | ||||||
chr5:56890819
|
A | G | 14 | a0001c0005t0014g0321a0001c0005t0014g0322a0001c0005t0014g0323others(11): Show | 14 | HG01081.hp2 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.4389+2462A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890819 | ||||||
chr5:56890881
|
C | A | 1 | a0001c0001t0002g0292 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.4389+2524C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890881 | ||||||
chr5:56891036
|
C | T | 2 | a0003c0002t0009g0036a0003c0002t0017g0215 | 2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4390-2495C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891036 | ||||||
chr5:56891148
|
A | AC | 18 | a0001c0011t0009g0204a0001c0011t0009g0207a0001c0011t0025g0205others(15): Show | 19 | HG00642.hp1 HG01081.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.4390-2371dupC | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr5 | 56891148 | |||||
chr5:56891148
|
A | C | 1 | a0002c0003t0006g0137 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.4390-2383A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891148 | ||||||
chr5:56891148
|
AC | A | 48 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0027others(45): Show | 61 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.4390-2371delC | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr5 | 56891148 | |||||
chr5:56891148
|
ACCC | A | 186 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(183): Show | 201 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.4390-2373_4390-237 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr5 | 56891148 | |||||
chr5:56891151
|
C | A | 1 | a0001c0001t0002g0293 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4390-2380C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891151 | ||||||
chr5:56891153
|
C | A | 3 | a0001c0001t0017g0328a0003c0002t0004g0038a0003c0002t0005g0037 | 3 | HG01891.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4390-2378C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891153 | ||||||
chr5:56891157
|
C | A | 81 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0027others(78): Show | 94 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.4390-2374C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891157 | ||||||
chr5:56891159
|
C | A | 143 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(140): Show | 158 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.4390-2372C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891159 | ||||||
chr5:56891160
|
CA | C | 4 | a0001c0008t0009g0209a0002c0004t0005g0076a0002c0004t0005g0106others(1): Show | 4 | HG03225.hp1 HG03492.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.4390-2370delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891160 | ||||||
chr5:56891160
|
CACA | C | 4 | a0001c0005t0014g0321a0001c0005t0014g0322a0001c0005t0014g0323others(1): Show | 4 | HG02451.hp1 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.4390-2370_4390-236 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891160 | ||||||
chr5:56891161
|
A | C | 15 | a0001c0008t0009g0208a0001c0008t0009g0210a0001c0008t0009g0212others(12): Show | 15 | HG01081.hp2 HG01943.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.4390-2370A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891161 | ||||||
chr5:56891163
|
A | C | 6 | a0001c0005t0014g0325a0001c0008t0009g0208a0001c0008t0009g0209others(3): Show | 6 | HG01884.hp2 HG02809.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.4390-2368A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891163 | ||||||
chr5:56891248
|
G | A | 3 | a0001c0001t0002g0213a0001c0001t0002g0279a0001c0001t0008g0300 | 3 | HG00738.hp2 HG01074.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.4390-2283G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891248 | ||||||
chr5:56891272
|
G | A | 1 | a0001c0001t0002g0219 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4390-2259G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891272 | ||||||
chr5:56891370
|
A | G | 1 | a0002c0003t0013g0125 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4390-2161A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891370 | ||||||
chr5:56891506
|
G | A | 1 | a0002c0004t0005g0047 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4390-2025G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891506 | ||||||
chr5:56891563
|
T | C | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.4390-1968T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891563 | ||||||
chr5:56891749
|
A | C | 1 | a0001c0005t0001g0235 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.4390-1782A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891749 | ||||||
chr5:56891988
|
TTTTGGCT others(8): Show |
T | 1 | a0001c0005t0004g0234 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.4390-1542_4390-152 others(19): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891988 | ||||||
chr5:56892021
|
C | T | 1 | a0002c0003t0027g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4390-1510C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892021 | ||||||
chr5:56892185
|
T | G | 12 | a0003c0002t0001g0030a0003c0002t0001g0031a0003c0002t0004g0038others(9): Show | 13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.4390-1346T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892185 | ||||||
chr5:56892544
|
C | G | 60 | a0003c0002t0001g0171a0003c0002t0001g0174a0003c0002t0003g0002others(57): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.4390-987C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892544 | ||||||
chr5:56892589
|
A | G | 1 | a0001c0001t0002g0284 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4390-942A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892589 | ||||||
chr5:56892742
|
G | C | 222 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(219): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.4390-789G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892742 | ||||||
chr5:56892916
|
T | C | 7 | a0003c0002t0003g0011a0003c0002t0003g0032a0003c0002t0003g0033others(4): Show | 8 | HG00558.hp1 HG00597.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.4390-615T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892916 | ||||||
chr5:56892967
|
CT | C | 23 | a0001c0001t0002g0288a0001c0001t0009g0335a0001c0001t0010g0029others(20): Show | 25 | HG00621.hp1 HG01167.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.4390-555delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr5 | 56892967 | |||||
chr5:56892972
|
T | TA | 15 | a0001c0005t0004g0234a0001c0005t0014g0321a0001c0005t0014g0322others(12): Show | 15 | HG01081.hp2 HG01884.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.4390-559_4390-558i others(3): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892972 | ||||||
chr5:56892973
|
T | A | 201 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(198): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.4390-558T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892973 | ||||||
chr5:56892974
|
T | A | 222 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(219): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.4390-557T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892974 | ||||||
chr5:56892975
|
T | A | 222 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(219): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.4390-556T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892975 | ||||||
chr5:56892976
|
T | A | 319 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(316): Show | 350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.4390-555T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892976 | ||||||
chr5:56893083
|
T | C | 2 | a0001c0001t0002g0280a0001c0001t0002g0295 | 2 | HG00609.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.4390-448T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893083 | ||||||
chr5:56893100
|
T | C | 1 | a0003c0002t0011g0163 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4390-431T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893100 | ||||||
chr5:56893104
|
T | C | 222 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(219): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.4390-427T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893104 | ||||||
chr5:56893150
|
G | A | 222 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0024others(219): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.4390-381G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893150 | ||||||
chr5:56893204
|
A | G | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.4390-327A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893204 | ||||||
chr5:56893290
|
G | C | 1 | a0002c0003t0001g0091 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4390-241G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893290 | ||||||
chr5:56893344
|
G | C | 4 | a0003c0009t0015g0028a0003c0009t0019g0326a0003c0009t0019g0327others(1): Show | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4390-187G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893344 | ||||||
chr5:56893383
|
C | T | 6 | a0003c0002t0007g0012a0003c0002t0007g0039a0003c0002t0007g0040others(3): Show | 7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.4390-148C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893383 | ||||||
chr5:56893423
|
C | T | 10 | a0001c0001t0009g0335a0001c0001t0010g0029a0001c0001t0010g0329others(7): Show | 11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.4390-108C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893423 |