geneid | 646851 |
---|---|
ensemblid | ENSG00000184949.18 |
hgncid | 44197 |
symbol | FAM227A |
name | family with sequence similarity 227 member A |
refseq_nuc | NM_001013647.2 |
refseq_prot | NP_001013669.1 |
ensembl_nuc | ENST00000535113.7 |
ensembl_prot | ENSP00000445093.1 |
mane_status | MANE Select |
chr | chr22 |
start | 38578118 |
end | 38656392 |
strand | - |
ver | v1.2 |
region | chr22:38578118-38656392 |
region5000 | chr22:38573118-38661392 |
regionname0 | FAM227A_chr22_38578118_38656392 |
regionname5000 | FAM227A_chr22_38573118_38661392 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 570 | 284 | 73 | 52 | 118 | 14 | 25 | 88 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0002 | 0/0 | 570 | 43 | 9 | 0 | 33 | 0 | 1 | 29 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0003 | 0/0 | 570 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1713 | 277 | 66 | 52 | 118 | 14 | 25 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
c0002 | 0/0 | 1713 | 42 | 8 | 0 | 33 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
c0003 | 0/0 | 1713 | 5 | 5 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
c0004 | 0/0 | 1713 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
c0005 | 0/0 | 1713 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
c0006 | 0/0 | 1713 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
c0007 | 0/0 | 1713 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 8375 | 81 | 8 | 13 | 45 | 6 | 8 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0002 | 0/0 | 8381 | 38 | 7 | 2 | 23 | 2 | 4 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0003 | 0/0 | 8380 | 38 | 0 | 4 | 30 | 0 | 4 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0004 | 0/0 | 8382 | 21 | 0 | 0 | 20 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0005 | 0/0 | 8376 | 12 | 2 | 7 | 0 | 1 | 2 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0006 | 0/0 | 8376 | 10 | 9 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0007 | 0/0 | 8376 | 10 | 6 | 1 | 2 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0008 | 0/0 | 8376 | 9 | 7 | 2 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0009 | 0/0 | 8381 | 9 | 9 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0010 | 0/0 | 8376 | 7 | 0 | 2 | 3 | 1 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0011 | 0/0 | 8382 | 7 | 7 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0012 | 0/0 | 8375 | 6 | 0 | 3 | 0 | 2 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0013 | 0/0 | 8378 | 5 | 5 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0014 | 0/0 | 8376 | 5 | 0 | 4 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0015 | 0/0 | 8381 | 5 | 0 | 0 | 5 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0016 | 0/0 | 8381 | 4 | 4 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0017 | 0/1 | 8381 | 4 | 1 | 1 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0018 | 0/0 | 8377 | 3 | 3 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0019 | 0/0 | 8375 | 3 | 0 | 3 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0020 | 0/0 | 8382 | 3 | 0 | 0 | 3 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0021 | 0/0 | 8382 | 3 | 1 | 1 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0022 | 0/0 | 8382 | 3 | 0 | 0 | 2 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0023 | 0/0 | 8377 | 2 | 2 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0024 | 0/0 | 8375 | 2 | 0 | 2 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0025 | 0/0 | 8383 | 2 | 0 | 0 | 2 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0026 | 0/0 | 8379 | 2 | 0 | 0 | 2 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0027 | 0/0 | 8381 | 2 | 1 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0028 | 0/0 | 8375 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0029 | 0/0 | 8375 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0030 | 0/0 | 8376 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0031 | 0/0 | 8375 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0032 | 0/0 | 8379 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0033 | 0/0 | 8376 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0034 | 0/0 | 8376 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0035 | 0/0 | 8377 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0036 | 0/0 | 8376 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0037 | 0/0 | 8376 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0038 | 0/0 | 8376 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0039 | 0/0 | 8376 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0040 | 0/0 | 8375 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0041 | 0/0 | 8375 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0042 | 0/0 | 8375 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0043 | 0/0 | 8375 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0044 | 0/0 | 8375 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0045 | 0/0 | 8376 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0046 | 0/0 | 8383 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0047 | 0/0 | 8382 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0048 | 0/0 | 8382 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0049 | 0/0 | 8379 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0050 | 0/0 | 8380 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0051 | 0/0 | 8381 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0052 | 0/0 | 8380 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0053 | 0/0 | 8381 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0054 | 0/0 | 8381 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0055 | 0/0 | 8381 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0056 | 0/0 | 8381 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0057 | 0/0 | 8380 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0058 | 0/0 | 8381 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
t0059 | 0/0 | 8381 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0093 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1713 | 277 | 66 | 52 | 118 | 14 | 25 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0003 | 0/0 | 1713 | 5 | 5 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0006 | 0/0 | 1713 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0007 | 0/0 | 1713 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0002c0002 | 0/0 | 1713 | 42 | 8 | 0 | 33 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0002c0004 | 0/0 | 1713 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0003c0005 | 0/0 | 1713 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 10087 | 81 | 8 | 13 | 45 | 6 | 8 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0002 | 0/0 | 10093 | 38 | 7 | 2 | 23 | 2 | 4 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0003 | 0/0 | 10092 | 38 | 0 | 4 | 30 | 0 | 4 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0005 | 0/0 | 10088 | 12 | 2 | 7 | 0 | 1 | 2 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0006 | 0/0 | 10088 | 10 | 9 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0007 | 0/0 | 10088 | 10 | 6 | 1 | 2 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0008 | 0/0 | 10088 | 8 | 6 | 2 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0009 | 0/0 | 10093 | 9 | 9 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0010 | 0/0 | 10088 | 7 | 0 | 2 | 3 | 1 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0012 | 0/0 | 10087 | 6 | 0 | 3 | 0 | 2 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0014 | 0/0 | 10088 | 5 | 0 | 4 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0016 | 0/0 | 10093 | 4 | 4 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0017 | 0/1 | 10093 | 4 | 1 | 1 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0018 | 0/0 | 10089 | 3 | 3 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0019 | 0/0 | 10087 | 3 | 0 | 3 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0021 | 0/0 | 10094 | 3 | 1 | 1 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0022 | 0/0 | 10094 | 3 | 0 | 0 | 2 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0023 | 0/0 | 10089 | 2 | 2 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0024 | 0/0 | 10087 | 2 | 0 | 2 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0027 | 0/0 | 10093 | 2 | 1 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0028 | 0/0 | 10087 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0029 | 0/0 | 10087 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0030 | 0/0 | 10088 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0031 | 0/0 | 10087 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0033 | 0/0 | 10088 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0034 | 0/0 | 10088 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0035 | 0/0 | 10089 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0036 | 0/0 | 10088 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0037 | 0/0 | 10088 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0038 | 0/0 | 10088 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0039 | 0/0 | 10088 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0040 | 0/0 | 10087 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0041 | 0/0 | 10087 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0042 | 0/0 | 10087 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0043 | 0/0 | 10087 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0044 | 0/0 | 10087 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0045 | 0/0 | 10088 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0050 | 0/0 | 10092 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0051 | 0/0 | 10093 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0052 | 0/0 | 10092 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0053 | 0/0 | 10093 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0054 | 0/0 | 10093 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0055 | 0/0 | 10093 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0056 | 0/0 | 10093 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0057 | 0/0 | 10092 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0058 | 0/0 | 10093 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0001t0059 | 0/0 | 10093 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0003t0013 | 0/0 | 10090 | 4 | 4 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0003t0032 | 0/0 | 10091 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0006t0008 | 0/0 | 10088 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0001c0007t0013 | 0/0 | 10090 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0002c0002t0004 | 0/0 | 10094 | 20 | 0 | 0 | 19 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0002c0002t0011 | 0/0 | 10094 | 7 | 7 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0002c0002t0015 | 0/0 | 10093 | 5 | 0 | 0 | 5 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0002c0002t0020 | 0/0 | 10094 | 3 | 0 | 0 | 3 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0002c0002t0025 | 0/0 | 10095 | 2 | 0 | 0 | 2 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0002c0002t0026 | 0/0 | 10091 | 2 | 0 | 0 | 2 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0002c0002t0047 | 0/0 | 10094 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0002c0002t0048 | 0/0 | 10094 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0002c0002t0049 | 0/0 | 10091 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0002c0004t0046 | 0/0 | 10095 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
a0003c0005t0004 | 0/0 | 10094 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | copy fasta | chr22 | 38573118 | 38661392 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0093 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0005g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0005g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0005g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0005g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0005g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0006g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0007g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0007g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0007g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0008g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0008g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0009g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0009g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0009g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0009g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0009g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0009g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0009g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0009g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0010g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0010g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0010g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0010g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0010g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0010g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0010g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0012g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0012g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0012g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0012g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0012g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0012g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0014g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0014g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0014g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0014g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0014g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0016g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0016g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0016g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0016g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0017g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0017g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0017g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0017g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0018g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0018g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0018g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0019g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0019g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0019g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0021g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0021g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0021g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0022g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0022g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0022g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0023g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0023g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0024g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0024g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0027g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0027g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0028g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0029g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0030g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0031g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0033g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0034g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0035g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0036g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0037g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0038g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0039g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0040g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0041g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0042g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0043g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0044g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0045g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0050g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0051g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0052g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0053g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0054g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0055g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0056g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0057g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0058g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0001t0059g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0003t0013g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0003t0013g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0003t0013g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0003t0013g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0003t0032g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0006t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0001c0007t0013g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0011g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0011g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0011g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0011g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0011g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0011g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0015g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0015g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0015g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0015g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0015g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0020g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0020g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0020g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0025g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0025g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0026g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0026g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0047g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0048g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0002t0049g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0002c0004t0046g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
a0003c0005t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0014 | g0167 | EUR | GBR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | GBR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00280 | hp1 | a0001 | c0001 | t0017 | g0283 | EUR | FIN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | FIN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | FIN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0249 | EUR | FIN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00408 | hp2 | a0002 | c0002 | t0025 | g0192 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00423 | hp2 | a0001 | c0001 | t0027 | g0265 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00642 | hp1 | a0001 | c0001 | t0051 | g0276 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00673 | hp2 | a0002 | c0002 | t0004 | g0191 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0264 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00735 | hp1 | a0001 | c0001 | t0005 | g0141 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00735 | hp2 | a0001 | c0001 | t0014 | g0165 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00738 | hp2 | a0001 | c0001 | t0019 | g0135 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00741 | hp1 | a0001 | c0001 | t0010 | g0102 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01069 | hp1 | a0001 | c0001 | t0024 | g0096 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01069 | hp2 | a0001 | c0001 | t0014 | g0166 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01071 | hp2 | a0001 | c0001 | t0024 | g0095 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01074 | hp2 | a0001 | c0001 | t0019 | g0136 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01081 | hp1 | a0001 | c0001 | t0010 | g0097 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01081 | hp2 | a0001 | c0001 | t0012 | g0117 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01167 | hp1 | a0001 | c0001 | t0012 | g0116 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01169 | hp2 | a0001 | c0001 | t0012 | g0011 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01175 | hp2 | a0001 | c0001 | t0007 | g0132 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01243 | hp1 | a0001 | c0001 | t0041 | g0052 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01243 | hp2 | a0001 | c0001 | t0008 | g0040 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01256 | hp1 | a0001 | c0001 | t0014 | g0163 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01256 | hp2 | a0001 | c0001 | t0043 | g0073 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01258 | hp1 | a0001 | c0001 | t0014 | g0164 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01261 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01261 | hp2 | a0001 | c0001 | t0036 | g0137 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01346 | hp1 | a0001 | c0001 | t0021 | g0257 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01433 | hp1 | a0001 | c0001 | t0017 | g0288 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01433 | hp2 | a0001 | c0001 | t0008 | g0042 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01515 | hp1 | a0001 | c0001 | t0012 | g0114 | EUR | IBS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | IBS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0037 | EUR | IBS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01517 | hp1 | a0001 | c0001 | t0012 | g0115 | EUR | IBS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01891 | hp1 | a0001 | c0001 | t0059 | g0310 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01891 | hp2 | a0002 | c0002 | t0011 | g0208 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01928 | hp2 | a0001 | c0001 | t0005 | g0142 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01934 | hp1 | a0001 | c0001 | t0019 | g0138 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01934 | hp2 | a0001 | c0001 | t0006 | g0024 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01975 | hp2 | a0001 | c0001 | t0005 | g0019 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01981 | hp1 | a0001 | c0001 | t0005 | g0018 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01981 | hp2 | a0001 | c0001 | t0042 | g0145 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0260 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0016 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02015 | hp2 | a0002 | c0002 | t0004 | g0193 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02027 | hp1 | a0001 | c0001 | t0022 | g0248 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02027 | hp2 | a0001 | c0001 | t0038 | g0153 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0290 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0033 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02055 | hp2 | a0001 | c0001 | t0016 | g0294 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02056 | hp2 | a0001 | c0001 | t0044 | g0143 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02083 | hp2 | a0002 | c0002 | t0004 | g0190 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02129 | hp1 | a0001 | c0001 | t0010 | g0148 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02135 | hp2 | a0001 | c0001 | t0058 | g0272 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02145 | hp1 | a0002 | c0002 | t0011 | g0173 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02155 | hp1 | a0001 | c0001 | t0050 | g0271 | EAS | CDX | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CDX | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | CDX | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02258 | hp1 | a0001 | c0001 | t0045 | g0127 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02258 | hp2 | a0001 | c0003 | t0013 | g0159 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02280 | hp1 | a0001 | c0001 | t0018 | g0168 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0299 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0014 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02300 | hp2 | a0001 | c0001 | t0029 | g0133 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02451 | hp2 | a0001 | c0001 | t0021 | g0258 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0039 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02622 | hp2 | a0001 | c0001 | t0009 | g0309 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02698 | hp2 | a0001 | c0001 | t0021 | g0259 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02717 | hp1 | a0001 | c0007 | t0013 | g0157 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02717 | hp2 | a0002 | c0004 | t0046 | g0210 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02735 | hp2 | a0001 | c0001 | t0012 | g0113 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02809 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02809 | hp2 | a0001 | c0001 | t0006 | g0026 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0027 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0131 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02886 | hp1 | a0001 | c0001 | t0018 | g0169 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0323 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02895 | hp2 | a0001 | c0001 | t0009 | g0322 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02896 | hp1 | a0001 | c0001 | t0009 | g0217 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02896 | hp2 | a0002 | c0002 | t0011 | g0175 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02897 | hp1 | a0001 | c0001 | t0009 | g0218 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02897 | hp2 | a0001 | c0001 | t0009 | g0306 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02922 | hp2 | a0001 | c0001 | t0023 | g0140 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0066 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02976 | hp1 | a0001 | c0001 | t0018 | g0170 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02976 | hp2 | a0001 | c0001 | t0023 | g0032 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03041 | hp1 | a0001 | c0001 | t0016 | g0311 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03041 | hp2 | a0001 | c0001 | t0035 | g0129 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03098 | hp1 | a0001 | c0003 | t0032 | g0156 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03098 | hp2 | a0001 | c0001 | t0027 | g0302 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03130 | hp1 | a0001 | c0001 | t0009 | g0313 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0035 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03139 | hp2 | a0002 | c0002 | t0011 | g0199 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03195 | hp1 | a0001 | c0001 | t0057 | g0278 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03195 | hp2 | a0001 | c0001 | t0030 | g0038 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03209 | hp2 | a0001 | c0001 | t0034 | g0162 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0092 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03225 | hp2 | a0001 | c0001 | t0016 | g0296 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03453 | hp1 | a0002 | c0002 | t0011 | g0198 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03486 | hp2 | a0001 | c0001 | t0009 | g0312 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0297 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03516 | hp2 | a0002 | c0002 | t0011 | g0205 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0030 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03540 | hp2 | a0001 | c0003 | t0013 | g0160 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03579 | hp1 | a0001 | c0001 | t0009 | g0305 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03579 | hp2 | a0001 | c0001 | t0007 | g0063 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0270 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03669 | hp1 | a0001 | c0001 | t0033 | g0155 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0268 | SAS | STU | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | STU | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03834 | hp1 | a0001 | c0001 | t0010 | g0099 | SAS | BEB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03834 | hp2 | a0001 | c0001 | t0053 | g0253 | SAS | BEB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03927 | hp1 | a0001 | c0001 | t0022 | g0245 | SAS | BEB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03927 | hp2 | a0001 | c0001 | t0007 | g0080 | SAS | BEB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0320 | SAS | STU | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | STU | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG04184 | hp1 | a0002 | c0002 | t0004 | g0214 | SAS | BEB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18522 | hp1 | a0001 | c0006 | t0008 | g0034 | AFR | YRI | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0041 | AFR | YRI | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | CHB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18747 | hp1 | a0001 | c0001 | t0052 | g0286 | EAS | CHB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0291 | AFR | YRI | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0292 | AFR | YRI | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18939 | hp2 | a0001 | c0001 | t0031 | g0154 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18943 | hp1 | a0002 | c0002 | t0004 | g0200 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18944 | hp1 | a0002 | c0002 | t0020 | g0174 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18948 | hp2 | a0001 | c0001 | t0028 | g0074 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18952 | hp2 | a0002 | c0002 | t0015 | g0188 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18960 | hp1 | a0002 | c0002 | t0025 | g0194 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18960 | hp2 | a0001 | c0001 | t0055 | g0243 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18962 | hp1 | a0002 | c0002 | t0004 | g0180 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18963 | hp2 | a0001 | c0001 | t0010 | g0061 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18964 | hp2 | a0002 | c0002 | t0020 | g0186 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18974 | hp2 | a0002 | c0002 | t0004 | g0213 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18979 | hp2 | a0002 | c0002 | t0004 | g0171 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18980 | hp1 | a0002 | c0002 | t0004 | g0183 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18982 | hp1 | a0003 | c0005 | t0004 | g0179 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18983 | hp2 | a0002 | c0002 | t0047 | g0202 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18988 | hp2 | a0002 | c0002 | t0004 | g0203 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18990 | hp1 | a0002 | c0002 | t0004 | g0211 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18991 | hp1 | a0002 | c0002 | t0004 | g0178 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18993 | hp1 | a0002 | c0002 | t0004 | g0184 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18994 | hp2 | a0002 | c0002 | t0026 | g0196 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18995 | hp1 | a0001 | c0001 | t0037 | g0130 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19000 | hp2 | a0001 | c0001 | t0007 | g0150 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19011 | hp1 | a0001 | c0001 | t0040 | g0009 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19012 | hp1 | a0002 | c0002 | t0004 | g0185 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19030 | hp2 | a0001 | c0001 | t0017 | g0318 | AFR | LWK | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19057 | hp1 | a0002 | c0002 | t0004 | g0182 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19060 | hp2 | a0002 | c0002 | t0015 | g0187 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19062 | hp1 | a0001 | c0001 | t0054 | g0321 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19064 | hp1 | a0002 | c0002 | t0026 | g0195 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19064 | hp2 | a0001 | c0001 | t0039 | g0081 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19065 | hp2 | a0002 | c0002 | t0004 | g0204 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19067 | hp1 | a0001 | c0001 | t0007 | g0077 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19068 | hp2 | a0002 | c0002 | t0004 | g0212 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19076 | hp2 | a0002 | c0002 | t0015 | g0209 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19079 | hp1 | a0002 | c0002 | t0004 | g0172 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19080 | hp1 | a0002 | c0002 | t0004 | g0181 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19082 | hp2 | a0001 | c0001 | t0010 | g0059 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19084 | hp2 | a0002 | c0002 | t0048 | g0176 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19085 | hp1 | a0002 | c0002 | t0020 | g0197 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19086 | hp1 | a0002 | c0002 | t0015 | g0177 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19086 | hp2 | a0001 | c0001 | t0022 | g0222 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19087 | hp2 | a0002 | c0002 | t0004 | g0201 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19088 | hp1 | a0002 | c0002 | t0015 | g0189 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0069 | AFR | YRI | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA19240 | hp2 | a0002 | c0002 | t0049 | g0207 | AFR | YRI | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | ASW | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA20129 | hp2 | a0002 | c0002 | t0011 | g0206 | AFR | ASW | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA20752 | hp1 | a0001 | c0001 | t0010 | g0098 | EUR | TSI | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0315 | EUR | TSI | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0263 | SAS | GIH | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA20905 | hp2 | a0001 | c0001 | t0005 | g0031 | SAS | GIH | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02109 | hp2 | a0001 | c0003 | t0013 | g0161 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02559 | hp1 | a0001 | c0001 | t0016 | g0295 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03471 | hp1 | a0001 | c0001 | t0056 | g0304 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG03471 | hp2 | a0001 | c0001 | t0008 | g0043 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG06807 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | USA | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
HG06807 | hp2 | a0001 | c0003 | t0013 | g0158 | AFR | USA | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA20300 | hp1 | a0001 | c0001 | t0008 | g0036 | AFR | USA | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | USA | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | LWK | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | LWK | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0017 | g0277 | REF | REF | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0093 | REF | REF | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:38597330
|
A | T | 1 | a0003 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.1406T>A | p.Val469Asp | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/17 | 1773/10087 | 1406/1713 | 469/570 | chr22 | 38597330 | ||
chr22:38638781
|
C | T | 2 | a0002a0003 | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
missense_variant | MODERATE | c.337G>A | p.Glu113Lys | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/17 | 704/10087 | 337/1713 | 113/570 | chr22 | 38638781 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:38599826
|
G | A | 1 | a0001c0006 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.1317C>T | p.Ala439Ala | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/17 | 1684/10087 | 1317/1713 | 439/570 | chr22 | 38599826 | ||
chr22:38599874
|
G | A | 1 | a0001c0007 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.1269C>T | p.Asn423Asn | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/17 | 1636/10087 | 1269/1713 | 423/570 | chr22 | 38599874 | ||
chr22:38623236
|
C | T | 1 | a0002c0004 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.894G>A | p.Ser298Ser | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/17 | 1261/10087 | 894/1713 | 298/570 | chr22 | 38623236 | ||
chr22:38638776
|
G | A | 1 | a0001c0003 | 5 | HG02109.hp2 HG02258.hp2 HG03098.hp1 others(2): Show |
synonymous_variant | LOW | c.342C>T | p.Leu114Leu | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/17 | 709/10087 | 342/1713 | 114/570 | chr22 | 38638776 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:38578149
|
C | A | 30 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(27): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*7976G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7976 | chr22 | 38578149 | |||||
chr22:38578504
|
T | C | 1 | a0001c0001t0024 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7621A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7621 | chr22 | 38578504 | |||||
chr22:38578564
|
T | C | 8 | a0002c0002t0004a0002c0002t0015a0002c0002t0020others(5): Show | 35 | HG00408.hp2 HG00673.hp2 HG02015.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*7561A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7561 | chr22 | 38578564 | |||||
chr22:38578675
|
C | T | 36 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(33): Show | 171 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*7450G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7450 | chr22 | 38578675 | |||||
chr22:38578755
|
C | T | 1 | a0001c0001t0033 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7370G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7370 | chr22 | 38578755 | |||||
chr22:38578756
|
G | A | 1 | a0002c0002t0047 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7369C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7369 | chr22 | 38578756 | |||||
chr22:38578778
|
A | G | 1 | a0001c0001t0039 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7347T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7347 | chr22 | 38578778 | |||||
chr22:38578794
|
C | G | 1 | a0001c0001t0042 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7331G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7331 | chr22 | 38578794 | |||||
chr22:38578848
|
A | G | 1 | a0001c0001t0041 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7277T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7277 | chr22 | 38578848 | |||||
chr22:38579098
|
C | T | 3 | a0001c0001t0019a0001c0001t0029a0001c0001t0036 | 5 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7027G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7027 | chr22 | 38579098 | |||||
chr22:38579441
|
A | G | 1 | a0001c0001t0038 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6684T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 6684 | chr22 | 38579441 | |||||
chr22:38579506
|
G | A | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 207 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*6619C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 6619 | chr22 | 38579506 | |||||
chr22:38579540
|
G | A | 1 | a0002c0002t0048 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6585C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 6585 | chr22 | 38579540 | |||||
chr22:38580039
|
G | A | 1 | a0001c0001t0043 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6086C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 6086 | chr22 | 38580039 | |||||
chr22:38580096
|
T | TTTTA | 30 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(27): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*6028_*6029insTAAA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 6028 | chr22 | 38580096 | |||||
chr22:38580130
|
G | A | 3 | a0001c0001t0005a0001c0001t0035a0001c0001t0037 | 14 | HG00735.hp1 HG01261.hp1 HG01516.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5995C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 5995 | chr22 | 38580130 | |||||
chr22:38580345
|
T | C | 1 | a0001c0001t0055 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5780A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 5780 | chr22 | 38580345 | |||||
chr22:38580508
|
CTGTT | C | 1 | a0001c0001t0018 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5613_*5616delAACA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 5613 | chr22 | 38580508 | |||||
chr22:38580814
|
C | G | 1 | a0002c0002t0020 | 3 | NA18944.hp1 NA18964.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5311G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 5311 | chr22 | 38580814 | |||||
chr22:38580954
|
T | C | 1 | a0001c0001t0056 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5171A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 5171 | chr22 | 38580954 | |||||
chr22:38581036
|
C | T | 1 | a0001c0001t0040 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5089G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 5089 | chr22 | 38581036 | |||||
chr22:38581068
|
C | T | 4 | a0001c0001t0005a0001c0001t0006a0001c0001t0035others(1): Show | 24 | HG00735.hp1 HG01261.hp1 HG01516.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5057G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 5057 | chr22 | 38581068 | |||||
chr22:38581093
|
T | A | 1 | a0001c0001t0044 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5032A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 5032 | chr22 | 38581093 | |||||
chr22:38581742
|
G | GT | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(20): Show | 127 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*4382dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 4382 | chr22 | 38581742 | |||||
chr22:38581742
|
G | GTT | 5 | a0001c0001t0022a0001c0001t0027a0001c0001t0058others(2): Show | 12 | HG00423.hp2 HG02027.hp1 HG02135.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4381_*4382dupAA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 4382 | chr22 | 38581742 | |||||
chr22:38581742
|
G | GTTT | 8 | a0002c0002t0004a0002c0002t0011a0002c0002t0020others(5): Show | 36 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*4380_*4382dupAAA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 4382 | chr22 | 38581742 | |||||
chr22:38581845
|
C | T | 1 | a0001c0001t0018 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4280G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 4280 | chr22 | 38581845 | |||||
chr22:38581846
|
G | A | 1 | a0001c0001t0045 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4279C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 4279 | chr22 | 38581846 | |||||
chr22:38581885
|
G | C | 15 | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(12): Show | 97 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*4240C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 4240 | chr22 | 38581885 | |||||
chr22:38582072
|
G | C | 2 | a0001c0001t0009a0001c0001t0059 | 10 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4053C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 4053 | chr22 | 38582072 | |||||
chr22:38582164
|
A | G | 6 | a0001c0001t0014a0001c0001t0033a0001c0001t0034others(3): Show | 13 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3961T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 3961 | chr22 | 38582164 | |||||
chr22:38582257
|
G | T | 1 | a0001c0001t0054 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3868C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 3868 | chr22 | 38582257 | |||||
chr22:38582504
|
G | A | 1 | a0001c0001t0037 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3621C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 3621 | chr22 | 38582504 | |||||
chr22:38582861
|
C | T | 1 | a0001c0001t0006 | 10 | HG01934.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3264G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 3264 | chr22 | 38582861 | |||||
chr22:38582969
|
G | A | 1 | a0001c0001t0058 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3156C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 3156 | chr22 | 38582969 | |||||
chr22:38583013
|
C | G | 1 | a0001c0001t0053 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3112G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 3112 | chr22 | 38583013 | |||||
chr22:38583115
|
C | T | 1 | a0001c0001t0014 | 5 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3010G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 3010 | chr22 | 38583115 | |||||
chr22:38583171
|
C | CT | 26 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(23): Show | 119 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*2953dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 2953 | chr22 | 38583171 | |||||
chr22:38583171
|
C | CTT | 5 | a0001c0001t0021a0001c0001t0023a0001c0003t0013others(2): Show | 11 | HG01346.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2952_*2953dupAA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 2953 | chr22 | 38583171 | |||||
chr22:38583204
|
C | T | 1 | a0001c0001t0031 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2921G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 2921 | chr22 | 38583204 | |||||
chr22:38583230
|
T | C | 7 | a0001c0001t0003a0001c0001t0017a0001c0001t0027others(4): Show | 48 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2895A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 2895 | chr22 | 38583230 | |||||
chr22:38583809
|
C | T | 1 | a0001c0001t0030 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2316G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 2316 | chr22 | 38583809 | |||||
chr22:38584407
|
C | G | 1 | a0001c0001t0029 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1718G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 1718 | chr22 | 38584407 | |||||
chr22:38584466
|
C | T | 1 | a0001c0001t0018 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1659G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 1659 | chr22 | 38584466 | |||||
chr22:38584797
|
A | T | 2 | a0001c0001t0012a0001c0001t0052 | 7 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1328T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 1328 | chr22 | 38584797 | |||||
chr22:38585005
|
C | T | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0016others(13): Show | 101 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1120G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 1120 | chr22 | 38585005 | |||||
chr22:38585037
|
T | C | 1 | a0001c0001t0051 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1088A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 1088 | chr22 | 38585037 | |||||
chr22:38585044
|
T | C | 1 | a0001c0001t0051 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1081A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 1081 | chr22 | 38585044 | |||||
chr22:38585047
|
A | G | 1 | a0001c0001t0051 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1078T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 1078 | chr22 | 38585047 | |||||
chr22:38585110
|
T | G | 1 | a0001c0001t0059 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1015A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 1015 | chr22 | 38585110 | |||||
chr22:38585371
|
C | T | 1 | a0001c0001t0028 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*754G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 754 | chr22 | 38585371 | |||||
chr22:38585720
|
C | T | 1 | a0001c0001t0050 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*405G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 405 | chr22 | 38585720 | |||||
chr22:38586026
|
C | A | 11 | a0002c0002t0004a0002c0002t0011a0002c0002t0015others(8): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*99G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 99 | chr22 | 38586026 | |||||
chr22:38656150
|
G | A | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(15): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-125C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/17 | chr22 | 38656150 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:38586316
|
T | C | 157 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1639-117A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586316 | ||||||
chr22:38586353
|
C | G | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1639-154G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586353 | ||||||
chr22:38586436
|
G | A | 1 | a0001c0001t0037g0130 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1639-237C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586436 | ||||||
chr22:38586437
|
T | A | 100 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(97): Show | 101 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1639-238A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586437 | ||||||
chr22:38586654
|
G | A | 8 | a0001c0001t0009g0292a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1639-455C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586654 | ||||||
chr22:38586738
|
A | G | 195 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(192): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.1639-539T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586738 | ||||||
chr22:38586839
|
G | GT | 4 | a0001c0001t0016g0294a0001c0001t0016g0295a0001c0001t0016g0296others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1639-641dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586839 | ||||||
chr22:38586913
|
C | T | 4 | a0001c0001t0016g0294a0001c0001t0016g0295a0001c0001t0016g0296others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1639-714G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586913 | ||||||
chr22:38586914
|
G | A | 8 | a0001c0001t0009g0292a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1639-715C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586914 | ||||||
chr22:38587089
|
AAC | A | 7 | a0001c0001t0014g0163a0001c0001t0014g0164a0001c0001t0014g0165others(4): Show | 7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1639-892_1639-891d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38587089 | ||||||
chr22:38587174
|
A | G | 7 | a0001c0001t0009g0292a0001c0001t0009g0305a0001c0001t0009g0306others(4): Show | 7 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1639-975T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38587174 | ||||||
chr22:38587553
|
A | G | 4 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0042others(1): Show | 4 | HG01243.hp2 HG01433.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1639-1354T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38587553 | ||||||
chr22:38587696
|
T | C | 1 | a0001c0001t0002g0234 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1639-1497A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38587696 | ||||||
chr22:38587704
|
G | GT | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1639-1506dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38587704 | ||||||
chr22:38588475
|
C | T | 7 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(4): Show | 7 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1639-2276G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588475 | ||||||
chr22:38588480
|
G | A | 4 | a0001c0001t0006g0017a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG01934.hp2 HG02559.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1639-2281C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588480 | ||||||
chr22:38588499
|
G | C | 1 | a0001c0001t0040g0009 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1639-2300C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588499 | ||||||
chr22:38588615
|
T | TA | 50 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0057others(47): Show | 50 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1639-2417dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588615 | ||||||
chr22:38588615
|
TA | T | 6 | a0001c0001t0001g0111a0001c0001t0001g0123a0001c0001t0001g0144others(3): Show | 6 | HG00323.hp1 HG01346.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1639-2417delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588615 | ||||||
chr22:38588764
|
C | CA | 6 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0151others(3): Show | 6 | HG00140.hp1 HG00438.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.1639-2566dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588764 | ||||||
chr22:38588764
|
CA | C | 149 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(146): Show | 150 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1639-2566delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588764 | ||||||
chr22:38588780
|
T | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0014a0001c0001t0005g0016others(21): Show | 24 | HG00735.hp1 HG01261.hp1 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.1639-2581A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588780 | ||||||
chr22:38588841
|
T | C | 7 | a0001c0001t0009g0292a0001c0001t0009g0305a0001c0001t0009g0306others(4): Show | 7 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1638+2594A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588841 | ||||||
chr22:38588945
|
A | G | 7 | a0001c0001t0014g0163a0001c0001t0014g0164a0001c0001t0014g0165others(4): Show | 7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1638+2490T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588945 | ||||||
chr22:38589060
|
T | C | 157 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1638+2375A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38589060 | ||||||
chr22:38589254
|
G | C | 1 | a0002c0002t0004g0182 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1638+2181C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38589254 | ||||||
chr22:38589309
|
TGGACTTC | T | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1638+2119_1638+212 others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38589309 | ||||||
chr22:38589352
|
T | C | 1 | a0001c0001t0002g0315 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1638+2083A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38589352 | ||||||
chr22:38589698
|
T | C | 1 | a0002c0004t0046g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1638+1737A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38589698 | ||||||
chr22:38589813
|
A | C | 96 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(93): Show | 97 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1638+1622T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38589813 | ||||||
chr22:38589944
|
T | C | 1 | a0003c0005t0004g0179 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1638+1491A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38589944 | ||||||
chr22:38590086
|
C | CACAAA | 141 | a0001c0001t0001g0051a0001c0001t0002g0004a0001c0001t0002g0216others(138): Show | 142 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1638+1344_1638+134 others(9): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38590086 | ||||||
chr22:38590086
|
C | CACAAAAC others(3): Show |
17 | a0001c0001t0002g0251a0001c0001t0003g0220a0001c0001t0003g0229others(14): Show | 17 | HG02135.hp2 HG02165.hp2 HG02896.hp1 others(14): Show |
intron_variant | MODIFIER | c.1638+1339_1638+134 others(14): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38590086 | ||||||
chr22:38590086
|
C | CACAAAAC others(8): Show |
1 | a0001c0001t0003g0287 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1638+1334_1638+134 others(19): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38590086 | ||||||
chr22:38590086
|
C | CACAAAAC others(13): Show |
2 | a0001c0001t0018g0169a0001c0001t0018g0170 | 2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1638+1329_1638+134 others(24): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38590086 | ||||||
chr22:38590086
|
CACAAAAC others(3): Show |
C | 1 | a0001c0001t0010g0099 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1638+1339_1638+134 others(14): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38590086 | ||||||
chr22:38590243
|
G | A | 160 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(157): Show | 161 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.1638+1192C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38590243 | ||||||
chr22:38590279
|
CA | C | 103 | a0001c0001t0001g0010a0001c0001t0001g0123a0001c0001t0002g0004others(100): Show | 104 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1638+1155delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38590279 | ||||||
chr22:38590279
|
CAA | C | 8 | a0001c0001t0002g0240a0001c0001t0002g0255a0001c0001t0002g0274others(5): Show | 8 | HG02895.hp1 HG02922.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.1638+1154_1638+115 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38590279 | ||||||
chr22:38591290
|
C | G | 1 | a0001c0001t0009g0309 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1638+145G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38591290 | ||||||
chr22:38591407
|
T | G | 3 | a0001c0001t0002g0240a0001c0001t0002g0254a0001c0001t0003g0233 | 3 | HG00558.hp1 NA18975.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1638+28A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38591407 | ||||||
chr22:38591631
|
C | T | 1 | a0001c0001t0005g0037 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1533-91G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38591631 | ||||||
chr22:38591722
|
T | C | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1533-182A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38591722 | ||||||
chr22:38591747
|
C | T | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1533-207G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38591747 | ||||||
chr22:38591874
|
G | A | 1 | a0001c0001t0030g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1533-334C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38591874 | ||||||
chr22:38592066
|
A | C | 7 | a0001c0001t0014g0163a0001c0001t0014g0164a0001c0001t0014g0165others(4): Show | 7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1533-526T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38592066 | ||||||
chr22:38592110
|
A | G | 171 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(168): Show | 172 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.1533-570T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38592110 | ||||||
chr22:38592339
|
C | T | 321 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(318): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1533-799G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38592339 | ||||||
chr22:38592380
|
C | T | 1 | a0002c0002t0004g0185 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1533-840G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38592380 | ||||||
chr22:38592472
|
G | T | 7 | a0001c0001t0014g0163a0001c0001t0014g0164a0001c0001t0014g0165others(4): Show | 7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1533-932C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38592472 | ||||||
chr22:38592514
|
G | T | 1 | a0001c0001t0018g0169 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1533-974C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38592514 | ||||||
chr22:38592605
|
TTAAATCA others(11): Show |
T | 2 | a0001c0001t0023g0032a0001c0001t0023g0140 | 2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1533-1083_1533-106 others(22): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38592605 | ||||||
chr22:38592622
|
G | A | 1 | a0001c0001t0003g0231 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1533-1082C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38592622 | ||||||
chr22:38593002
|
C | G | 100 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(97): Show | 101 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1533-1462G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593002 | ||||||
chr22:38593361
|
C | T | 1 | a0002c0002t0011g0199 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1533-1821G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593361 | ||||||
chr22:38593379
|
C | T | 2 | a0002c0002t0004g0178a0002c0002t0015g0209 | 2 | NA18991.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1533-1839G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593379 | ||||||
chr22:38593499
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0071 | 2 | HG00438.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.1533-1959G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593499 | ||||||
chr22:38593600
|
A | G | 2 | a0001c0001t0023g0032a0001c0001t0023g0140 | 2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1533-2060T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593600 | ||||||
chr22:38593622
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG01071.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1533-2082G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593622 | ||||||
chr22:38593641
|
T | C | 157 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1533-2101A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593641 | ||||||
chr22:38593808
|
A | G | 157 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1533-2268T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593808 | ||||||
chr22:38593857
|
A | G | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1533-2317T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593857 | ||||||
chr22:38594657
|
G | A | 169 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(166): Show | 170 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.1532+2547C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38594657 | ||||||
chr22:38594677
|
T | C | 3 | a0001c0001t0003g0232a0001c0001t0003g0267a0001c0001t0003g0273 | 3 | NA18939.hp1 NA18975.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1532+2527A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38594677 | ||||||
chr22:38594690
|
C | T | 3 | a0001c0001t0021g0257a0001c0001t0021g0258a0001c0001t0021g0259 | 3 | HG01346.hp1 HG02451.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1532+2514G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38594690 | ||||||
chr22:38594733
|
C | T | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.1532+2471G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38594733 | ||||||
chr22:38595350
|
C | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0014a0001c0001t0005g0016others(21): Show | 24 | HG00735.hp1 HG01261.hp1 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.1532+1854G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595350 | ||||||
chr22:38595388
|
G | T | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.1532+1816C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595388 | ||||||
chr22:38595492
|
G | A | 7 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(4): Show | 7 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1532+1712C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595492 | ||||||
chr22:38595710
|
C | T | 1 | a0001c0001t0030g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1532+1494G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595710 | ||||||
chr22:38595746
|
T | C | 1 | a0002c0002t0026g0196 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1532+1458A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595746 | ||||||
chr22:38595871
|
T | C | 4 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0323others(1): Show | 4 | HG02280.hp2 HG02895.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1532+1333A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595871 | ||||||
chr22:38595885
|
A | G | 1 | a0001c0001t0028g0074 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1532+1319T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595885 | ||||||
chr22:38595896
|
A | T | 1 | a0001c0001t0041g0052 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1532+1308T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595896 | ||||||
chr22:38595970
|
AG | A | 294 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(291): Show | 298 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1532+1233delC | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595970 | ||||||
chr22:38595972
|
G | C | 5 | a0001c0001t0009g0292a0001c0001t0009g0305a0001c0001t0009g0306others(2): Show | 5 | HG00642.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1532+1232C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595972 | ||||||
chr22:38595973
|
G | C | 105 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(102): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1532+1231C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595973 | ||||||
chr22:38596178
|
G | A | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1532+1026C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38596178 | ||||||
chr22:38596226
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1532+978G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38596226 | ||||||
chr22:38596368
|
G | A | 1 | a0001c0001t0003g0289 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1532+836C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38596368 | ||||||
chr22:38596444
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1532+760C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38596444 | ||||||
chr22:38596962
|
G | A | 2 | a0001c0001t0018g0169a0001c0001t0018g0170 | 2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1532+242C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38596962 | ||||||
chr22:38597365
|
C | T | 96 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(93): Show | 97 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1380-9G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38597365 | ||||||
chr22:38597397
|
G | A | 1 | a0001c0001t0057g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1380-41C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38597397 | ||||||
chr22:38597462
|
A | G | 157 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1380-106T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38597462 | ||||||
chr22:38597471
|
A | G | 12 | a0002c0002t0004g0178a0002c0002t0004g0190a0002c0002t0004g0191others(9): Show | 12 | HG00408.hp2 HG00673.hp2 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380-115T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38597471 | ||||||
chr22:38597512
|
G | A | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1380-156C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38597512 | ||||||
chr22:38597942
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1380-586G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38597942 | ||||||
chr22:38597958
|
G | A | 96 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(93): Show | 97 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1380-602C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38597958 | ||||||
chr22:38597971
|
A | C | 96 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(93): Show | 97 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1380-615T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38597971 | ||||||
chr22:38598042
|
C | CAAAAAA | 69 | a0001c0001t0002g0004a0001c0001t0002g0219a0001c0001t0002g0223others(66): Show | 70 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.1380-692_1380-687d others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598042 | ||||||
chr22:38598042
|
C | CAAAAAAA | 34 | a0001c0001t0002g0216a0001c0001t0002g0241a0001c0001t0002g0291others(31): Show | 34 | HG01175.hp1 HG01891.hp1 HG02135.hp2 others(31): Show |
intron_variant | MODIFIER | c.1380-693_1380-687d others(9): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598042 | ||||||
chr22:38598042
|
C | CAAAAAAA others(1): Show |
43 | a0001c0001t0003g0230a0001c0001t0003g0287a0001c0001t0009g0305others(40): Show | 43 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.1380-694_1380-687d others(10): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598042 | ||||||
chr22:38598042
|
C | CAAAAAAA others(2): Show |
6 | a0001c0001t0016g0294a0002c0002t0004g0212a0002c0002t0011g0173others(3): Show | 6 | HG02055.hp2 HG02145.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1380-695_1380-687d others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598042 | ||||||
chr22:38598042
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0018g0168 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1380-696_1380-687d others(12): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598042 | ||||||
chr22:38598135
|
G | A | 4 | a0001c0001t0001g0048a0001c0001t0001g0068a0001c0001t0001g0076others(1): Show | 4 | NA18959.hp2 NA18965.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1380-779C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598135 | ||||||
chr22:38598572
|
C | T | 170 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(167): Show | 171 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.1379+1192G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598572 | ||||||
chr22:38598761
|
C | T | 6 | a0001c0003t0013g0158a0001c0003t0013g0159a0001c0003t0013g0160others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379+1003G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598761 | ||||||
chr22:38598824
|
A | T | 1 | a0001c0001t0007g0066 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1379+940T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598824 | ||||||
chr22:38598851
|
T | C | 5 | a0001c0001t0003g0220a0001c0001t0003g0229a0001c0001t0003g0230others(2): Show | 5 | NA18980.hp2 NA18983.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.1379+913A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598851 | ||||||
chr22:38598957
|
C | CT | 76 | a0001c0001t0001g0090a0001c0001t0002g0219a0001c0001t0002g0274others(73): Show | 76 | HG00280.hp1 HG00423.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.1379+806dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598957 | ||||||
chr22:38598957
|
CT | C | 6 | a0001c0001t0002g0252a0001c0001t0014g0163a0001c0001t0014g0164others(3): Show | 6 | HG00558.hp2 HG00735.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1379+806delA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598957 | ||||||
chr22:38599047
|
C | T | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1379+717G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599047 | ||||||
chr22:38599121
|
G | T | 2 | a0001c0001t0002g0240a0001c0001t0002g0254 | 2 | HG00558.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1379+643C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599121 | ||||||
chr22:38599214
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0090 | 2 | NA19009.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1379+550C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599214 | ||||||
chr22:38599345
|
C | A | 1 | a0001c0001t0001g0053 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1379+419G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599345 | ||||||
chr22:38599380
|
G | T | 157 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1379+384C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599380 | ||||||
chr22:38599385
|
A | G | 2 | a0002c0002t0025g0192a0002c0002t0025g0194 | 2 | HG00408.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1379+379T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599385 | ||||||
chr22:38599392
|
T | C | 6 | a0001c0003t0013g0158a0001c0003t0013g0159a0001c0003t0013g0160others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379+372A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599392 | ||||||
chr22:38599539
|
A | G | 4 | a0001c0001t0001g0048a0001c0001t0001g0068a0001c0001t0001g0076others(1): Show | 4 | NA18959.hp2 NA18965.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379+225T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599539 | ||||||
chr22:38599566
|
C | T | 14 | a0001c0001t0002g0223a0001c0001t0002g0224a0001c0001t0002g0225others(11): Show | 14 | HG00609.hp2 HG01099.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.1379+198G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599566 | ||||||
chr22:38599621
|
G | A | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1379+143C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599621 | ||||||
chr22:38599676
|
C | A | 13 | a0001c0001t0002g0223a0001c0001t0002g0224a0001c0001t0002g0225others(10): Show | 13 | HG00609.hp2 HG01099.hp1 HG03927.hp1 others(10): Show |
intron_variant | MODIFIER | c.1379+88G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599676 | ||||||
chr22:38599685
|
C | T | 6 | a0001c0003t0013g0158a0001c0003t0013g0159a0001c0003t0013g0160others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379+79G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599685 | ||||||
chr22:38599753
|
G | C | 1 | a0001c0001t0022g0248 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1379+11C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599753 | ||||||
chr22:38600308
|
G | C | 1 | a0002c0004t0046g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1222-387C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600308 | ||||||
chr22:38600316
|
G | GTA | 79 | a0001c0001t0002g0315a0001c0001t0002g0324a0001c0001t0003g0220others(76): Show | 79 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1222-397_1222-396d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600316 | ||||||
chr22:38600316
|
G | GTATA | 7 | a0001c0001t0014g0163a0001c0001t0014g0164a0001c0001t0014g0165others(4): Show | 7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1222-399_1222-396d others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600316 | ||||||
chr22:38600316
|
GTA | G | 9 | a0001c0001t0001g0065a0001c0001t0001g0118a0001c0001t0007g0002others(6): Show | 10 | HG01175.hp2 HG02258.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1222-397_1222-396d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600316 | ||||||
chr22:38600648
|
T | C | 2 | a0001c0001t0003g0232a0001c0001t0003g0267 | 2 | NA18939.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1222-727A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600648 | ||||||
chr22:38600723
|
C | T | 3 | a0001c0001t0021g0257a0001c0001t0021g0258a0001c0001t0021g0259 | 3 | HG01346.hp1 HG02451.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1222-802G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600723 | ||||||
chr22:38600860
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0082 | 3 | HG01516.hp2 HG01517.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1222-939C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600860 | ||||||
chr22:38600900
|
C | T | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1222-979G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600900 | ||||||
chr22:38600929
|
C | T | 1 | a0001c0001t0002g0297 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1222-1008G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600929 | ||||||
chr22:38600950
|
C | CA | 24 | a0001c0001t0005g0005a0001c0001t0005g0014a0001c0001t0005g0016others(21): Show | 24 | HG00735.hp1 HG01261.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.1222-1030dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600950 | ||||||
chr22:38600950
|
CA | C | 11 | a0001c0001t0009g0217a0001c0001t0009g0218a0001c0001t0009g0292others(8): Show | 11 | HG01891.hp1 HG02451.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1222-1030delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600950 | ||||||
chr22:38601011
|
C | T | 1 | a0001c0001t0017g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1222-1090G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38601011 | ||||||
chr22:38601109
|
C | T | 1 | a0001c0001t0002g0242 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1222-1188G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38601109 | ||||||
chr22:38601264
|
C | G | 195 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(192): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.1222-1343G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38601264 | ||||||
chr22:38601878
|
A | G | 8 | a0001c0001t0009g0292a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222-1957T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38601878 | ||||||
chr22:38601953
|
G | T | 1 | a0001c0001t0002g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1222-2032C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38601953 | ||||||
chr22:38602060
|
G | C | 47 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0228others(44): Show | 47 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1222-2139C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38602060 | ||||||
chr22:38602206
|
C | G | 6 | a0001c0003t0013g0158a0001c0003t0013g0159a0001c0003t0013g0160others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222-2285G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38602206 | ||||||
chr22:38602408
|
A | G | 1 | a0001c0001t0002g0226 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1222-2487T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38602408 | ||||||
chr22:38602514
|
C | A | 154 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(151): Show | 155 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1222-2593G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38602514 | ||||||
chr22:38602777
|
C | T | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1221+2477G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38602777 | ||||||
chr22:38602801
|
C | T | 1 | a0001c0001t0008g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1221+2453G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38602801 | ||||||
chr22:38603071
|
G | A | 1 | a0001c0001t0051g0276 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1221+2183C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38603071 | ||||||
chr22:38603116
|
T | C | 194 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(191): Show | 195 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1221+2138A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38603116 | ||||||
chr22:38603230
|
C | T | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1221+2024G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38603230 | ||||||
chr22:38603487
|
C | CA | 140 | a0001c0001t0001g0079a0001c0001t0002g0004a0001c0001t0002g0216others(137): Show | 141 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1221+1766dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38603487 | ||||||
chr22:38603487
|
C | CAA | 12 | a0001c0001t0002g0308a0001c0001t0003g0230a0001c0001t0009g0217others(9): Show | 12 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1221+1765_1221+176 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38603487 | ||||||
chr22:38603801
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0139 | 2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1221+1453C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38603801 | ||||||
chr22:38603817
|
T | C | 6 | a0001c0001t0012g0011a0001c0001t0012g0113a0001c0001t0012g0114others(3): Show | 6 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1221+1437A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38603817 | ||||||
chr22:38603921
|
T | C | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1221+1333A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38603921 | ||||||
chr22:38604392
|
G | A | 98 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(95): Show | 99 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1221+862C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38604392 | ||||||
chr22:38604514
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1221+740C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38604514 | ||||||
chr22:38604655
|
T | A | 45 | a0001c0001t0009g0292a0002c0002t0004g0171a0002c0002t0004g0172others(42): Show | 45 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.1221+599A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38604655 | ||||||
chr22:38604971
|
T | C | 1 | a0002c0002t0011g0205 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1221+283A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38604971 | ||||||
chr22:38604991
|
A | T | 6 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(3): Show | 6 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1221+263T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38604991 | ||||||
chr22:38605156
|
T | C | 1 | a0001c0001t0044g0143 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1221+98A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38605156 | ||||||
chr22:38605747
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1127-399C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38605747 | ||||||
chr22:38606019
|
A | G | 1 | a0001c0001t0003g0238 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1127-671T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38606019 | ||||||
chr22:38606044
|
T | C | 1 | a0001c0001t0018g0169 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1127-696A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38606044 | ||||||
chr22:38606623
|
G | T | 2 | a0001c0001t0009g0217a0001c0001t0009g0218 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1126+766C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38606623 | ||||||
chr22:38606968
|
G | C | 1 | a0001c0001t0008g0042 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1126+421C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38606968 | ||||||
chr22:38607076
|
T | C | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1126+313A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38607076 | ||||||
chr22:38607092
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1126+297C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38607092 | ||||||
chr22:38607123
|
G | A | 1 | a0001c0001t0017g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1126+266C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38607123 | ||||||
chr22:38607176
|
C | CA | 43 | a0001c0001t0001g0013a0001c0001t0001g0050a0001c0001t0001g0056others(40): Show | 43 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.1126+212dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38607176 | ||||||
chr22:38607176
|
CA | C | 20 | a0001c0001t0001g0047a0001c0001t0001g0068a0001c0001t0001g0149others(17): Show | 20 | HG00408.hp2 HG00673.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1126+212delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38607176 | ||||||
chr22:38607176
|
CAA | C | 33 | a0002c0002t0004g0171a0002c0002t0004g0178a0002c0002t0004g0180others(30): Show | 33 | HG01891.hp2 HG02145.hp1 HG02896.hp2 others(30): Show |
intron_variant | MODIFIER | c.1126+211_1126+212d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38607176 | ||||||
chr22:38607292
|
G | C | 1 | a0001c0001t0001g0007 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1126+97C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38607292 | ||||||
chr22:38607325
|
C | T | 1 | a0001c0001t0034g0162 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1126+64G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38607325 | ||||||
chr22:38607490
|
G | A | 155 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(152): Show | 156 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.1039-14C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38607490 | ||||||
chr22:38607513
|
C | A | 2 | a0001c0001t0002g0216a0001c0001t0053g0253 | 2 | HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1039-37G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38607513 | ||||||
chr22:38607514
|
G | A | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1039-38C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38607514 | ||||||
chr22:38607768
|
T | C | 2 | a0001c0001t0001g0058a0001c0001t0001g0071 | 2 | HG00438.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.1039-292A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38607768 | ||||||
chr22:38607771
|
C | G | 1 | a0001c0001t0002g0314 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1039-295G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38607771 | ||||||
chr22:38607771
|
C | T | 1 | a0002c0002t0004g0182 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1039-295G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38607771 | ||||||
chr22:38608014
|
A | G | 1 | a0001c0001t0002g0314 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1039-538T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608014 | ||||||
chr22:38608065
|
A | G | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1039-589T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608065 | ||||||
chr22:38608080
|
A | G | 1 | a0001c0001t0003g0320 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1039-604T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608080 | ||||||
chr22:38608096
|
A | C | 1 | a0001c0001t0002g0308 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1039-620T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608096 | ||||||
chr22:38608113
|
C | A | 1 | a0001c0001t0002g0240 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1039-637G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608113 | ||||||
chr22:38608155
|
C | CA | 22 | a0001c0001t0001g0006a0001c0001t0001g0057a0001c0001t0001g0075others(19): Show | 22 | HG01175.hp2 HG01346.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.1039-680dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608155 | ||||||
chr22:38608155
|
CA | C | 121 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0126others(118): Show | 122 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1039-680delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608155 | ||||||
chr22:38608155
|
CAA | C | 13 | a0001c0001t0005g0005a0001c0001t0005g0014a0001c0001t0005g0016others(10): Show | 13 | HG00735.hp1 HG01261.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.1039-681_1039-680d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608155 | ||||||
chr22:38608155
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0007t0013g0157 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1039-690_1039-680d others(13): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608155 | ||||||
chr22:38608191
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1039-715C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608191 | ||||||
chr22:38608214
|
G | T | 1 | a0001c0001t0036g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1039-738C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608214 | ||||||
chr22:38608572
|
A | C | 95 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(92): Show | 96 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1039-1096T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608572 | ||||||
chr22:38608701
|
G | C | 1 | a0001c0001t0010g0059 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1039-1225C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608701 | ||||||
chr22:38608793
|
C | CT | 7 | a0001c0001t0001g0062a0001c0001t0001g0068a0001c0001t0001g0084others(4): Show | 7 | HG00741.hp1 HG01175.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-1318dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608793 | ||||||
chr22:38608793
|
CT | C | 195 | a0001c0001t0001g0060a0001c0001t0001g0064a0001c0001t0002g0004others(192): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.1039-1318delA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608793 | ||||||
chr22:38608832
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1039-1356C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608832 | ||||||
chr22:38608859
|
G | C | 1 | a0001c0001t0009g0313 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1039-1383C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608859 | ||||||
chr22:38608958
|
G | A | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1039-1482C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608958 | ||||||
chr22:38609021
|
A | G | 193 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(190): Show | 194 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1039-1545T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609021 | ||||||
chr22:38609057
|
A | T | 156 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(153): Show | 157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1039-1581T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609057 | ||||||
chr22:38609276
|
C | T | 1 | a0001c0001t0003g0262 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1039-1800G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609276 | ||||||
chr22:38609398
|
GT | G | 6 | a0001c0003t0013g0158a0001c0003t0013g0159a0001c0003t0013g0160others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039-1923delA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609398 | ||||||
chr22:38609522
|
A | T | 3 | a0001c0001t0012g0113a0001c0001t0012g0114a0001c0001t0012g0115 | 3 | HG01515.hp1 HG01517.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1039-2046T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609522 | ||||||
chr22:38609743
|
G | T | 1 | a0001c0001t0002g0323 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1039-2267C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609743 | ||||||
chr22:38609785
|
G | C | 2 | a0001c0001t0009g0217a0001c0001t0009g0218 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1039-2309C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609785 | ||||||
chr22:38609821
|
G | C | 1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1039-2345C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609821 | ||||||
chr22:38609833
|
G | A | 10 | a0001c0001t0009g0217a0001c0001t0009g0218a0001c0001t0009g0292others(7): Show | 10 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1039-2357C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609833 | ||||||
chr22:38609865
|
A | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(317): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1039-2389T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609865 | ||||||
chr22:38609992
|
C | T | 10 | a0001c0001t0006g0017a0001c0001t0006g0022a0001c0001t0006g0023others(7): Show | 10 | HG01934.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1039-2516G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609992 | ||||||
chr22:38610183
|
T | A | 42 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(39): Show | 42 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.1039-2707A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610183 | ||||||
chr22:38610184
|
A | T | 1 | a0001c0001t0003g0263 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039-2708T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610184 | ||||||
chr22:38610192
|
A | T | 13 | a0001c0001t0014g0163a0001c0001t0014g0164a0001c0001t0014g0165others(10): Show | 13 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1039-2716T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610192 | ||||||
chr22:38610193
|
T | A | 1 | a0002c0002t0015g0177 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1039-2717A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610193 | ||||||
chr22:38610273
|
C | T | 1 | a0001c0001t0027g0302 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1039-2797G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610273 | ||||||
chr22:38610527
|
C | CCT | 156 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(153): Show | 157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1039-3052_1039-305 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610527 | ||||||
chr22:38610628
|
G | A | 2 | a0002c0002t0004g0178a0002c0002t0015g0209 | 2 | NA18991.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1039-3152C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610628 | ||||||
chr22:38610743
|
T | C | 4 | a0002c0002t0004g0203a0002c0002t0004g0204a0002c0002t0004g0213others(1): Show | 4 | HG04184.hp1 NA18974.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-3267A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610743 | ||||||
chr22:38610791
|
G | A | 1 | a0001c0001t0030g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1039-3315C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610791 | ||||||
chr22:38610912
|
T | C | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1039-3436A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610912 | ||||||
chr22:38610929
|
A | G | 193 | a0001c0001t0001g0109a0001c0001t0002g0004a0001c0001t0002g0216others(190): Show | 194 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1039-3453T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610929 | ||||||
chr22:38610984
|
C | T | 1 | a0002c0002t0004g0204 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1039-3508G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610984 | ||||||
chr22:38610985
|
G | A | 1 | a0001c0001t0003g0228 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1039-3509C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610985 | ||||||
chr22:38611055
|
G | A | 8 | a0001c0001t0009g0292a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039-3579C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611055 | ||||||
chr22:38611067
|
GAAA | G | 13 | a0001c0001t0014g0163a0001c0001t0014g0164a0001c0001t0014g0165others(10): Show | 13 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1039-3594_1039-359 others(7): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611067 | ||||||
chr22:38611096
|
C | T | 3 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043 | 3 | HG01433.hp2 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1039-3620G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611096 | ||||||
chr22:38611158
|
G | C | 3 | a0001c0001t0012g0011a0001c0001t0012g0116a0001c0001t0012g0117 | 3 | HG01081.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1039-3682C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611158 | ||||||
chr22:38611169
|
A | C | 164 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0146others(161): Show | 165 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.1039-3693T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611169 | ||||||
chr22:38611187
|
C | G | 1 | a0001c0001t0059g0310 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1039-3711G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611187 | ||||||
chr22:38611262
|
T | TGA | 9 | a0001c0001t0001g0065a0001c0001t0001g0118a0001c0001t0007g0002others(6): Show | 10 | HG01175.hp2 HG02258.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1039-3788_1039-378 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611262 | ||||||
chr22:38611303
|
G | A | 10 | a0001c0001t0009g0217a0001c0001t0009g0218a0001c0001t0009g0292others(7): Show | 10 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1039-3827C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611303 | ||||||
chr22:38611321
|
A | G | 4 | a0001c0001t0016g0294a0001c0001t0016g0295a0001c0001t0016g0296others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-3845T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611321 | ||||||
chr22:38611353
|
C | A | 2 | a0002c0002t0011g0173a0002c0002t0011g0198 | 2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1039-3877G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611353 | ||||||
chr22:38611396
|
G | A | 23 | a0001c0001t0005g0005a0001c0001t0005g0014a0001c0001t0005g0016others(20): Show | 23 | HG00735.hp1 HG01261.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.1039-3920C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611396 | ||||||
chr22:38611445
|
A | G | 2 | a0002c0002t0011g0205a0002c0002t0049g0207 | 2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1039-3969T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611445 | ||||||
chr22:38611510
|
T | C | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1039-4034A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611510 | ||||||
chr22:38611650
|
G | A | 2 | a0001c0001t0002g0284a0001c0001t0002g0285 | 2 | NA18942.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1039-4174C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611650 | ||||||
chr22:38611658
|
T | C | 1 | a0001c0001t0006g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1039-4182A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611658 | ||||||
chr22:38611775
|
T | G | 1 | a0001c0001t0002g0256 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1039-4299A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611775 | ||||||
chr22:38611813
|
C | G | 6 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(3): Show | 6 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039-4337G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611813 | ||||||
chr22:38611926
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1039-4450C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611926 | ||||||
chr22:38611950
|
C | T | 2 | a0001c0001t0009g0217a0001c0001t0009g0218 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1039-4474G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611950 | ||||||
chr22:38612021
|
C | G | 1 | a0001c0001t0010g0059 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1039-4545G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38612021 | ||||||
chr22:38612419
|
C | A | 35 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(32): Show | 35 | HG00408.hp2 HG00673.hp2 HG02015.hp2 others(32): Show |
intron_variant | MODIFIER | c.1039-4943G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38612419 | ||||||
chr22:38612778
|
A | T | 1 | a0002c0004t0046g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1039-5302T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38612778 | ||||||
chr22:38612873
|
G | C | 1 | a0002c0004t0046g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1039-5397C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38612873 | ||||||
chr22:38613012
|
A | C | 4 | a0001c0001t0014g0163a0001c0001t0014g0164a0001c0001t0014g0165others(1): Show | 4 | HG00735.hp2 HG01069.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5536T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613012 | ||||||
chr22:38613012
|
A | G | 156 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(153): Show | 157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1039-5536T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613012 | ||||||
chr22:38613042
|
T | A | 1 | a0001c0001t0001g0100 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1039-5566A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613042 | ||||||
chr22:38613042
|
T | TTATATAT others(35): Show |
4 | a0001c0001t0002g0219a0001c0001t0002g0274a0001c0001t0002g0275others(1): Show | 4 | HG02922.hp1 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5608_1039-556 others(46): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613042 | ||||||
chr22:38613054
|
T | A | 1 | a0001c0001t0002g0284 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1039-5578A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613054 | ||||||
chr22:38613055
|
A | T | 1 | a0001c0001t0002g0284 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1039-5579T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613055 | ||||||
chr22:38613066
|
AATATATT others(37): Show |
A | 4 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0094others(1): Show | 4 | HG01928.hp1 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5634_1039-559 others(48): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613066 | ||||||
chr22:38613082
|
TTA | T | 20 | a0001c0001t0001g0048a0001c0001t0001g0068a0001c0001t0001g0076others(17): Show | 20 | HG01346.hp1 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1039-5608_1039-560 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613082 | ||||||
chr22:38613084
|
A | ATATATAT others(12): Show |
22 | a0002c0002t0004g0171a0002c0002t0004g0178a0002c0002t0004g0185others(19): Show | 22 | HG00408.hp2 HG00673.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1039-5609_1039-560 others(23): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613084 | ||||||
chr22:38613084
|
A | ATATATAT others(33): Show |
4 | a0002c0002t0020g0174a0002c0002t0020g0197a0002c0002t0048g0176others(1): Show | 4 | NA18944.hp1 NA18982.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-5609_1039-560 others(44): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613084 | ||||||
chr22:38613084
|
A | ATATATAT others(54): Show |
6 | a0002c0002t0004g0180a0002c0002t0004g0181a0002c0002t0004g0182others(3): Show | 6 | NA18962.hp1 NA18980.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039-5609_1039-560 others(65): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613084 | ||||||
chr22:38613084
|
A | ATATATAT others(11): Show |
1 | a0002c0002t0011g0199 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1039-5609_1039-560 others(22): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613084 | ||||||
chr22:38613086
|
A | ATATATTA others(69): Show |
5 | a0001c0001t0019g0135a0001c0001t0019g0136a0001c0001t0019g0138others(2): Show | 5 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1039-5611_1039-561 others(80): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613086 | ||||||
chr22:38613088
|
A | ATATATTA others(8): Show |
1 | a0002c0002t0011g0205 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1039-5613_1039-561 others(19): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613088 | ||||||
chr22:38613094
|
A | G | 2 | a0002c0002t0004g0171a0002c0002t0026g0195 | 2 | NA18979.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1039-5618T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613094 | ||||||
chr22:38613105
|
TTATA | T | 4 | a0001c0001t0016g0294a0001c0001t0016g0295a0001c0001t0016g0296others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5633_1039-563 others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613105 | ||||||
chr22:38613116
|
T | TATAATTA others(6): Show |
3 | a0002c0002t0011g0198a0002c0002t0011g0206a0002c0002t0011g0208 | 3 | HG01891.hp2 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1039-5641_1039-564 others(17): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613116 | ||||||
chr22:38613116
|
T | TATATAAT others(8): Show |
2 | a0002c0002t0011g0173a0002c0002t0011g0175 | 2 | HG02145.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1039-5641_1039-564 others(19): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613116 | ||||||
chr22:38613116
|
T | TATATAAT others(10): Show |
1 | a0002c0002t0049g0207 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1039-5641_1039-564 others(21): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613116 | ||||||
chr22:38613122
|
ATAAT | A | 4 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0323others(1): Show | 4 | HG02280.hp2 HG02895.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5650_1039-564 others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613122 | ||||||
chr22:38613130
|
A | T | 103 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(100): Show | 104 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1039-5654T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613130 | ||||||
chr22:38613140
|
T | C | 1 | a0001c0001t0005g0037 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1039-5664A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613140 | ||||||
chr22:38613168
|
G | GTATATAT others(27): Show |
1 | a0001c0001t0002g0242 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1039-5726_1039-569 others(38): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613168 | ||||||
chr22:38613172
|
ATATATTA others(18): Show |
A | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1039-5721_1039-569 others(29): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613172 | ||||||
chr22:38613185
|
AAT | A | 75 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0323others(72): Show | 75 | HG00408.hp2 HG00673.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1039-5711_1039-571 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613185 | ||||||
chr22:38613200
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0086 | 2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1039-5724A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613200 | ||||||
chr22:38613237
|
T | A | 1 | a0001c0001t0043g0073 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1039-5761A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613237 | ||||||
chr22:38613238
|
A | ATC | 146 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(143): Show | 147 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1039-5763_1039-576 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613238 | ||||||
chr22:38613238
|
A | C | 55 | a0001c0001t0002g0224a0001c0001t0005g0005a0001c0001t0005g0014others(52): Show | 55 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.1039-5762T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613238 | ||||||
chr22:38613239
|
A | T | 4 | a0001c0001t0016g0294a0001c0001t0016g0295a0001c0001t0016g0296others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5763T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613239 | ||||||
chr22:38613240
|
T | C | 4 | a0001c0001t0016g0294a0001c0001t0016g0295a0001c0001t0016g0296others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5764A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613240 | ||||||
chr22:38613246
|
A | T | 4 | a0001c0001t0016g0294a0001c0001t0016g0295a0001c0001t0016g0296others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5770T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613246 | ||||||
chr22:38613247
|
T | A | 4 | a0001c0001t0016g0294a0001c0001t0016g0295a0001c0001t0016g0296others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5771A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613247 | ||||||
chr22:38613254
|
CATATATT | C | 5 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(2): Show | 5 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039-5785_1039-577 others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613254 | ||||||
chr22:38613255
|
ATATAT | A | 3 | a0001c0001t0005g0019a0001c0001t0005g0142a0001c0001t0039g0081 | 3 | HG01928.hp2 HG01975.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1039-5784_1039-578 others(9): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613255 | ||||||
chr22:38613260
|
T | TTATATAT others(18): Show |
4 | a0001c0001t0006g0017a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG01934.hp2 HG02559.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-5785_1039-578 others(29): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613260 | ||||||
chr22:38613265
|
A | T | 5 | a0001c0001t0006g0017a0001c0001t0006g0023a0001c0001t0006g0024others(2): Show | 5 | HG01934.hp2 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1039-5789T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613265 | ||||||
chr22:38613272
|
T | A | 1 | a0001c0001t0010g0059 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1039-5796A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613272 | ||||||
chr22:38613272
|
TTATATAT others(9): Show |
T | 8 | a0001c0001t0009g0312a0001c0001t0014g0163a0001c0001t0014g0164others(5): Show | 8 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039-5812_1039-579 others(20): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613272 | ||||||
chr22:38613273
|
T | A | 4 | a0001c0001t0006g0017a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG01934.hp2 HG02559.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-5797A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613273 | ||||||
chr22:38613280
|
C | A | 4 | a0001c0001t0006g0017a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG01934.hp2 HG02559.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-5804G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613280 | ||||||
chr22:38613282
|
T | C | 4 | a0001c0001t0006g0017a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG01934.hp2 HG02559.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-5806A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613282 | ||||||
chr22:38613282
|
T | TATATAAT others(23): Show |
4 | a0001c0001t0006g0022a0001c0001t0006g0026a0001c0001t0006g0027others(1): Show | 4 | HG02451.hp1 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-5836_1039-580 others(34): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613282 | ||||||
chr22:38613289
|
T | TATATATA others(4): Show |
1 | a0001c0001t0018g0168 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1039-5814_1039-581 others(15): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613289 | ||||||
chr22:38613295
|
T | A | 1 | a0001c0001t0051g0276 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1039-5819A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613295 | ||||||
chr22:38613296
|
C | A | 1 | a0001c0001t0018g0168 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1039-5820G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613296 | ||||||
chr22:38613298
|
T | C | 1 | a0001c0001t0018g0168 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1039-5822A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613298 | ||||||
chr22:38613302
|
T | C | 2 | a0001c0001t0003g0270a0001c0001t0017g0288 | 2 | HG01433.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1039-5826A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613302 | ||||||
chr22:38613308
|
A | G | 1 | a0001c0001t0002g0242 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1039-5832T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613308 | ||||||
chr22:38613310
|
A | C | 1 | a0001c0001t0018g0168 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1039-5834T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613310 | ||||||
chr22:38613312
|
C | CATATAAT others(9): Show |
99 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(96): Show | 100 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1039-5852_1039-583 others(20): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613312 | ||||||
chr22:38613312
|
C | CATATAAT others(25): Show |
43 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(40): Show | 43 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.1039-5837_1039-583 others(36): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613312 | ||||||
chr22:38613312
|
C | CATATAAT others(41): Show |
1 | a0002c0002t0004g0181 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1039-5837_1039-583 others(52): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613312 | ||||||
chr22:38613312
|
C | CATATAAT others(7): Show |
2 | a0001c0001t0018g0169a0001c0001t0018g0170 | 2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1039-5837_1039-583 others(18): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613312 | ||||||
chr22:38613312
|
C | CATATATT | 6 | a0001c0001t0001g0056a0001c0001t0019g0135a0001c0001t0019g0136others(3): Show | 6 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-5837_1039-583 others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613312 | ||||||
chr22:38613312
|
C | T | 3 | a0001c0001t0009g0217a0001c0001t0009g0218a0001c0001t0018g0168 | 3 | HG02280.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1039-5836G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613312 | ||||||
chr22:38613341
|
A | T | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1039-5865T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613341 | ||||||
chr22:38613362
|
T | TTTATAAT others(66): Show |
1 | a0001c0001t0001g0056 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1039-5887_1039-588 others(77): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613362 | ||||||
chr22:38613362
|
T | TTTATAAT others(66): Show |
7 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0019g0135others(4): Show | 7 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039-5887_1039-588 others(77): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613362 | ||||||
chr22:38613363
|
C | T | 8 | a0001c0001t0001g0056a0001c0001t0001g0103a0001c0001t0001g0104others(5): Show | 8 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039-5887G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613363 | ||||||
chr22:38613363
|
CATATATA | C | 7 | a0001c0001t0014g0163a0001c0001t0014g0164a0001c0001t0014g0165others(4): Show | 7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039-5894_1039-588 others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613363 | ||||||
chr22:38613370
|
A | AAT | 8 | a0001c0001t0001g0056a0001c0001t0001g0103a0001c0001t0001g0104others(5): Show | 8 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039-5896_1039-589 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613370 | ||||||
chr22:38613370
|
A | AATATATA others(109): Show |
1 | a0001c0001t0059g0310 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1039-5895_1039-589 others(120): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613370 | ||||||
chr22:38613379
|
C | T | 7 | a0001c0001t0009g0292a0001c0001t0009g0305a0001c0001t0009g0306others(4): Show | 7 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039-5903G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613379 | ||||||
chr22:38613385
|
T | TTA | 9 | a0001c0001t0001g0056a0001c0001t0001g0103a0001c0001t0001g0104others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-5911_1039-591 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613385 | ||||||
chr22:38613396
|
A | T | 9 | a0001c0001t0001g0056a0001c0001t0001g0103a0001c0001t0001g0104others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-5920T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613396 | ||||||
chr22:38613397
|
T | A | 9 | a0001c0001t0001g0056a0001c0001t0001g0103a0001c0001t0001g0104others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-5921A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613397 | ||||||
chr22:38613399
|
T | TCATATAT others(155): Show |
1 | a0001c0001t0005g0019 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1039-5924_1039-592 others(166): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613399 | ||||||
chr22:38613399
|
T | TCATATAT others(149): Show |
2 | a0001c0001t0024g0095a0001c0001t0024g0096 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1039-5924_1039-592 others(160): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613399 | ||||||
chr22:38613400
|
T | A | 9 | a0001c0001t0001g0056a0001c0001t0001g0103a0001c0001t0001g0104others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-5924A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613400 | ||||||
chr22:38613403
|
TA | T | 3 | a0001c0001t0005g0019a0001c0001t0024g0095a0001c0001t0024g0096 | 3 | HG01069.hp1 HG01071.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1039-5928delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613403 | ||||||
chr22:38613404
|
A | AATATATA others(108): Show |
1 | a0001c0001t0053g0253 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1039-5929_1039-592 others(119): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | ||||||
chr22:38613404
|
A | AATATATA others(122): Show |
45 | a0001c0001t0018g0169a0001c0001t0018g0170a0002c0002t0004g0171others(42): Show | 45 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.1039-5929_1039-592 others(133): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | ||||||
chr22:38613404
|
A | AATATATA others(157): Show |
1 | a0001c0001t0018g0168 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1039-5929_1039-592 others(168): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | ||||||
chr22:38613404
|
A | AATATATA others(122): Show |
1 | a0002c0002t0004g0200 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1039-5929_1039-592 others(133): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | ||||||
chr22:38613404
|
A | AATATATA others(115): Show |
88 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(85): Show | 89 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1039-5929_1039-592 others(126): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | ||||||
chr22:38613404
|
A | AATATATA others(117): Show |
4 | a0001c0001t0009g0292a0001c0001t0009g0305a0001c0001t0009g0306others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5929_1039-592 others(128): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | ||||||
chr22:38613404
|
A | AATATATA others(122): Show |
9 | a0001c0001t0009g0217a0001c0001t0009g0218a0001c0001t0009g0309others(6): Show | 9 | HG02055.hp2 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-5929_1039-592 others(133): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | ||||||
chr22:38613404
|
A | AATATATA others(110): Show |
1 | a0001c0001t0002g0285 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1039-5929_1039-592 others(121): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | ||||||
chr22:38613404
|
A | AATATATA others(110): Show |
4 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0323others(1): Show | 4 | HG02280.hp2 HG02895.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5929_1039-592 others(121): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | ||||||
chr22:38613404
|
A | ATTAT | 9 | a0001c0001t0001g0056a0001c0001t0001g0103a0001c0001t0001g0104others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-5929_1039-592 others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | ||||||
chr22:38613413
|
G | A | 166 | a0001c0001t0001g0056a0001c0001t0001g0103a0001c0001t0001g0104others(163): Show | 167 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1039-5937C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613413 | ||||||
chr22:38613414
|
A | ATATATAA others(108): Show |
1 | a0001c0001t0003g0320 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1039-5939_1039-593 others(119): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | ||||||
chr22:38613414
|
A | ATATATAT others(117): Show |
7 | a0001c0001t0005g0005a0001c0001t0005g0020a0001c0001t0005g0021others(4): Show | 7 | HG00735.hp1 HG01261.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039-5939_1039-593 others(128): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | ||||||
chr22:38613414
|
A | ATATATAT others(108): Show |
1 | a0001c0001t0006g0030 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1039-5939_1039-593 others(119): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | ||||||
chr22:38613414
|
A | ATATATAT others(118): Show |
1 | a0001c0001t0014g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1039-5939_1039-593 others(129): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | ||||||
chr22:38613414
|
A | ATATATAT others(117): Show |
25 | a0001c0001t0005g0014a0001c0001t0005g0016a0001c0001t0005g0018others(22): Show | 25 | HG00735.hp2 HG01256.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1039-5939_1039-593 others(128): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | ||||||
chr22:38613414
|
A | ATATATAT others(115): Show |
1 | a0001c0001t0030g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1039-5939_1039-593 others(126): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | ||||||
chr22:38613414
|
A | ATATATAT others(109): Show |
2 | a0001c0001t0023g0032a0001c0001t0023g0140 | 2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1039-5939_1039-593 others(120): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | ||||||
chr22:38613414
|
A | ATATATAT others(111): Show |
8 | a0001c0001t0008g0033a0001c0001t0008g0035a0001c0001t0008g0036others(5): Show | 8 | HG01433.hp2 HG02055.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1039-5939_1039-593 others(122): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | ||||||
chr22:38613414
|
A | ATATATAT others(111): Show |
1 | a0001c0001t0017g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1039-5939_1039-593 others(122): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | ||||||
chr22:38613414
|
A | ATATATAT others(111): Show |
107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(104): Show | 110 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1039-5939_1039-593 others(122): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | ||||||
chr22:38613414
|
A | ATATATAT others(110): Show |
1 | a0001c0001t0014g0166 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1039-5939_1039-593 others(121): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | ||||||
chr22:38613414
|
A | ATATATAT others(110): Show |
1 | a0001c0001t0001g0012 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1039-5939_1039-593 others(121): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | ||||||
chr22:38613414
|
A | ATATATAT others(111): Show |
1 | a0001c0001t0008g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1039-5939_1039-593 others(122): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | ||||||
chr22:38613414
|
A | T | 166 | a0001c0001t0001g0056a0001c0001t0001g0103a0001c0001t0001g0104others(163): Show | 167 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1039-5938T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | ||||||
chr22:38613786
|
C | T | 1 | a0001c0001t0007g0150 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1039-6310G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613786 | ||||||
chr22:38613863
|
C | A | 1 | a0001c0007t0013g0157 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1038+6349G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613863 | ||||||
chr22:38613918
|
C | G | 1 | a0002c0002t0004g0182 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1038+6294G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613918 | ||||||
chr22:38613924
|
T | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0072 | 2 | NA18951.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1038+6288A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613924 | ||||||
chr22:38614022
|
C | T | 47 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170others(44): Show | 47 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.1038+6190G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614022 | ||||||
chr22:38614060
|
T | C | 2 | a0001c0001t0009g0217a0001c0001t0009g0218 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1038+6152A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614060 | ||||||
chr22:38614537
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1038+5675C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614537 | ||||||
chr22:38614630
|
A | T | 4 | a0001c0001t0016g0294a0001c0001t0016g0295a0001c0001t0016g0296others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+5582T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614630 | ||||||
chr22:38614761
|
A | T | 1 | a0001c0001t0014g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1038+5451T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614761 | ||||||
chr22:38614796
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1038+5416C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614796 | ||||||
chr22:38614805
|
A | AAGCC | 6 | a0001c0003t0013g0158a0001c0003t0013g0159a0001c0003t0013g0160others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+5403_1038+540 others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614805 | ||||||
chr22:38614871
|
T | C | 1 | a0002c0002t0004g0193 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1038+5341A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614871 | ||||||
chr22:38614900
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1038+5312T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614900 | ||||||
chr22:38614917
|
G | A | 1 | a0002c0002t0011g0199 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1038+5295C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614917 | ||||||
chr22:38615068
|
A | G | 1 | a0001c0001t0006g0029 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1038+5144T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38615068 | ||||||
chr22:38615187
|
T | A | 6 | a0001c0001t0005g0014a0001c0001t0005g0016a0001c0001t0005g0018others(3): Show | 6 | HG01928.hp2 HG01975.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+5025A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38615187 | ||||||
chr22:38615315
|
C | T | 6 | a0001c0001t0016g0294a0001c0001t0016g0295a0001c0001t0016g0296others(3): Show | 6 | HG02055.hp2 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+4897G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38615315 | ||||||
chr22:38616019
|
G | A | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1038+4193C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38616019 | ||||||
chr22:38616491
|
C | T | 1 | a0001c0001t0002g0224 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1038+3721G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38616491 | ||||||
chr22:38616509
|
A | C | 13 | a0001c0001t0014g0163a0001c0001t0014g0164a0001c0001t0014g0165others(10): Show | 13 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1038+3703T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38616509 | ||||||
chr22:38616666
|
C | CA | 12 | a0001c0001t0001g0068a0001c0001t0001g0125a0001c0001t0023g0032others(9): Show | 12 | HG00642.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1038+3545dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38616666 | ||||||
chr22:38616679
|
A | T | 10 | a0001c0001t0006g0017a0001c0001t0006g0022a0001c0001t0006g0023others(7): Show | 10 | HG01934.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1038+3533T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38616679 | ||||||
chr22:38616708
|
A | G | 1 | a0001c0001t0017g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1038+3504T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38616708 | ||||||
chr22:38616714
|
T | G | 5 | a0001c0001t0005g0014a0001c0001t0005g0016a0001c0001t0005g0018others(2): Show | 5 | HG01928.hp2 HG01975.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1038+3498A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38616714 | ||||||
chr22:38616846
|
G | T | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1038+3366C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38616846 | ||||||
chr22:38617065
|
G | C | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1038+3147C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617065 | ||||||
chr22:38617292
|
C | CT | 13 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0058others(10): Show | 13 | HG00408.hp1 HG00673.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1038+2919dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617292 | ||||||
chr22:38617292
|
CT | C | 146 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(143): Show | 147 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.1038+2919delA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617292 | ||||||
chr22:38617292
|
CTT | C | 6 | a0001c0001t0003g0287a0001c0001t0009g0313a0001c0001t0016g0296others(3): Show | 6 | HG00408.hp2 HG02896.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+2918_1038+291 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617292 | ||||||
chr22:38617354
|
G | A | 1 | a0001c0001t0005g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1038+2858C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617354 | ||||||
chr22:38617359
|
G | A | 3 | a0001c0001t0021g0257a0001c0001t0021g0258a0001c0001t0021g0259 | 3 | HG01346.hp1 HG02451.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1038+2853C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617359 | ||||||
chr22:38617381
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1038+2831G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617381 | ||||||
chr22:38617420
|
C | G | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.1038+2792G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617420 | ||||||
chr22:38617517
|
G | A | 91 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(88): Show | 92 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1038+2695C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617517 | ||||||
chr22:38617528
|
C | T | 1 | a0001c0001t0053g0253 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1038+2684G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617528 | ||||||
chr22:38617545
|
T | C | 4 | a0001c0001t0016g0294a0001c0001t0016g0295a0001c0001t0016g0296others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+2667A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617545 | ||||||
chr22:38617565
|
G | A | 6 | a0001c0001t0003g0228a0001c0001t0003g0279a0001c0001t0003g0280others(3): Show | 6 | HG00609.hp1 NA18951.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.1038+2647C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617565 | ||||||
chr22:38617568
|
T | C | 1 | a0001c0001t0052g0286 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1038+2644A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617568 | ||||||
chr22:38617591
|
G | A | 1 | a0002c0002t0011g0199 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1038+2621C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617591 | ||||||
chr22:38617763
|
C | T | 7 | a0002c0002t0004g0180a0002c0002t0004g0181a0002c0002t0004g0182others(4): Show | 7 | NA18962.hp1 NA18980.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.1038+2449G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617763 | ||||||
chr22:38617825
|
T | C | 154 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(151): Show | 155 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1038+2387A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617825 | ||||||
chr22:38617972
|
A | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0120 | 2 | NA18993.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1038+2240T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617972 | ||||||
chr22:38618046
|
T | C | 3 | a0001c0001t0012g0011a0001c0001t0012g0116a0001c0001t0012g0117 | 3 | HG01081.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1038+2166A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38618046 | ||||||
chr22:38618368
|
C | T | 1 | a0001c0001t0037g0130 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1038+1844G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38618368 | ||||||
chr22:38618666
|
AG | A | 4 | a0001c0001t0016g0294a0001c0001t0016g0295a0001c0001t0016g0296others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+1545delC | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38618666 | ||||||
chr22:38618777
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1038+1435G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38618777 | ||||||
chr22:38618805
|
G | A | 1 | a0001c0001t0057g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1038+1407C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38618805 | ||||||
chr22:38618939
|
C | G | 4 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0094others(1): Show | 4 | HG01928.hp1 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+1273G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38618939 | ||||||
chr22:38618971
|
G | GA | 17 | a0001c0001t0001g0054a0001c0001t0001g0104a0001c0001t0001g0121others(14): Show | 17 | HG00735.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1038+1240dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38618971 | ||||||
chr22:38619297
|
T | C | 157 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1038+915A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38619297 | ||||||
chr22:38619313
|
C | CTTAT | 8 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(5): Show | 8 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1038+895_1038+898d others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38619313 | ||||||
chr22:38619492
|
T | G | 1 | a0001c0001t0001g0075 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1038+720A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38619492 | ||||||
chr22:38620177
|
T | C | 170 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(167): Show | 171 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.1038+35A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38620177 | ||||||
chr22:38620203
|
C | G | 6 | a0001c0003t0013g0158a0001c0003t0013g0159a0001c0003t0013g0160others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+9G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38620203 | ||||||
chr22:38620398
|
A | G | 35 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0001g0118others(32): Show | 36 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.959-107T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38620398 | ||||||
chr22:38620424
|
A | G | 7 | a0001c0001t0014g0163a0001c0001t0014g0164a0001c0001t0014g0165others(4): Show | 7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.959-133T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38620424 | ||||||
chr22:38620458
|
T | TAA | 3 | a0001c0001t0001g0056a0001c0001t0001g0087a0001c0001t0001g0126 | 3 | NA18950.hp1 NA18961.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.959-168_959-167ins others(2): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38620458 | ||||||
chr22:38620638
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.959-347G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38620638 | ||||||
chr22:38620678
|
G | A | 46 | a0001c0001t0018g0169a0001c0001t0018g0170a0002c0002t0004g0171others(43): Show | 46 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(43): Show |
intron_variant | MODIFIER | c.959-387C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38620678 | ||||||
chr22:38620808
|
C | G | 1 | a0001c0001t0003g0320 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.959-517G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38620808 | ||||||
chr22:38620869
|
C | A | 1 | a0001c0001t0001g0008 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.959-578G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38620869 | ||||||
chr22:38620998
|
A | G | 1 | a0001c0001t0030g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.959-707T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38620998 | ||||||
chr22:38621074
|
C | T | 1 | a0001c0001t0010g0097 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.959-783G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38621074 | ||||||
chr22:38621316
|
C | G | 6 | a0001c0003t0013g0158a0001c0003t0013g0159a0001c0003t0013g0160others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.959-1025G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38621316 | ||||||
chr22:38621349
|
C | CA | 106 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(103): Show | 107 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.959-1059dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38621349 | ||||||
chr22:38621498
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.959-1207C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38621498 | ||||||
chr22:38621634
|
C | G | 1 | a0001c0001t0021g0259 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.959-1343G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38621634 | ||||||
chr22:38621666
|
C | T | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.959-1375G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38621666 | ||||||
chr22:38621888
|
C | T | 1 | a0001c0001t0005g0037 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.958+1284G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38621888 | ||||||
chr22:38621934
|
G | A | 1 | a0001c0001t0038g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.958+1238C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38621934 | ||||||
chr22:38622174
|
T | A | 242 | a0001c0001t0001g0065a0001c0001t0001g0088a0001c0001t0001g0100others(239): Show | 244 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.958+998A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622174 | ||||||
chr22:38622329
|
T | C | 157 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.958+843A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622329 | ||||||
chr22:38622404
|
C | T | 1 | a0001c0001t0002g0254 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.958+768G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622404 | ||||||
chr22:38622568
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.958+604C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622568 | ||||||
chr22:38622824
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.958+348G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622824 | ||||||
chr22:38622873
|
C | CA | 21 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0057others(18): Show | 21 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.958+298dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622873 | ||||||
chr22:38622873
|
CA | C | 148 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0091others(145): Show | 148 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.958+298delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622873 | ||||||
chr22:38622873
|
CAA | C | 39 | a0001c0001t0002g0004a0001c0001t0002g0250a0001c0001t0002g0297others(36): Show | 40 | HG00140.hp1 HG00408.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.958+297_958+298del others(2): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622873 | ||||||
chr22:38622873
|
CAAA | C | 12 | a0001c0001t0014g0166a0002c0002t0004g0204a0002c0002t0004g0212others(9): Show | 12 | HG01069.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.958+296_958+298del others(3): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622873 | ||||||
chr22:38623027
|
C | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0014a0001c0001t0005g0016others(21): Show | 24 | HG00735.hp1 HG01261.hp1 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.958+145G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38623027 | ||||||
chr22:38623359
|
G | T | 1 | a0001c0001t0057g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.851-80C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623359 | ||||||
chr22:38623363
|
GAGGATTG others(60): Show |
G | 1 | a0001c0001t0002g0284 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.851-151_851-85delT others(66): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623363 | ||||||
chr22:38623368
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.851-89A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623368 | ||||||
chr22:38623431
|
A | T | 1 | a0001c0001t0002g0284 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.851-152T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623431 | ||||||
chr22:38623433
|
T | A | 1 | a0001c0001t0002g0284 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.851-154A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623433 | ||||||
chr22:38623444
|
T | C | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.851-165A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623444 | ||||||
chr22:38623600
|
G | T | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.851-321C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623600 | ||||||
chr22:38623609
|
C | A | 1 | a0001c0001t0003g0264 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.851-330G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623609 | ||||||
chr22:38623848
|
C | T | 36 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0223others(33): Show | 37 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.851-569G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623848 | ||||||
chr22:38623876
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0105 | 2 | NA18995.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.851-597C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623876 | ||||||
chr22:38624031
|
G | A | 2 | a0001c0001t0024g0095a0001c0001t0024g0096 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.851-752C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38624031 | ||||||
chr22:38624203
|
G | A | 1 | a0001c0001t0003g0260 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.851-924C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38624203 | ||||||
chr22:38624261
|
C | A | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.851-982G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38624261 | ||||||
chr22:38624389
|
C | CA | 11 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0064others(8): Show | 11 | HG00733.hp1 HG01516.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.851-1111dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38624389 | ||||||
chr22:38624643
|
G | GGTGTCTA others(24): Show |
1 | a0001c0001t0002g0284 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.851-1395_851-1365d others(33): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38624643 | ||||||
chr22:38624802
|
C | T | 14 | a0001c0001t0005g0005a0001c0001t0005g0014a0001c0001t0005g0016others(11): Show | 14 | HG00735.hp1 HG01261.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.850+1378G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38624802 | ||||||
chr22:38625012
|
G | A | 4 | a0001c0001t0016g0294a0001c0001t0016g0295a0001c0001t0016g0296others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+1168C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625012 | ||||||
chr22:38625160
|
T | C | 163 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(160): Show | 164 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.850+1020A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625160 | ||||||
chr22:38625175
|
G | A | 1 | a0001c0001t0030g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.850+1005C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625175 | ||||||
chr22:38625304
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.850+876C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625304 | ||||||
chr22:38625320
|
C | T | 1 | a0001c0001t0006g0030 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.850+860G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625320 | ||||||
chr22:38625321
|
T | G | 194 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(191): Show | 195 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.850+859A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625321 | ||||||
chr22:38625368
|
G | A | 1 | a0001c0001t0030g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.850+812C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625368 | ||||||
chr22:38625385
|
C | T | 7 | a0001c0001t0009g0292a0001c0001t0009g0305a0001c0001t0009g0306others(4): Show | 7 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+795G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625385 | ||||||
chr22:38625387
|
C | CA | 19 | a0001c0001t0001g0047a0001c0001t0001g0057a0001c0001t0001g0146others(16): Show | 19 | HG01099.hp1 HG01516.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.850+792dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625387 | ||||||
chr22:38625387
|
CA | C | 8 | a0001c0001t0001g0119a0001c0001t0002g0004a0001c0001t0002g0246others(5): Show | 9 | HG02735.hp1 HG02895.hp2 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.850+792delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625387 | ||||||
chr22:38625517
|
G | A | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.850+663C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625517 | ||||||
chr22:38625712
|
G | A | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.850+468C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625712 | ||||||
chr22:38625830
|
G | GC | 163 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(160): Show | 164 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.850+349_850+350ins others(1): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625830 | ||||||
chr22:38625926
|
G | A | 4 | a0002c0002t0015g0177a0002c0002t0015g0187a0002c0002t0015g0188others(1): Show | 4 | NA18952.hp2 NA19060.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+254C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625926 | ||||||
chr22:38625930
|
G | A | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.850+250C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625930 | ||||||
chr22:38625943
|
C | CA | 36 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0079others(33): Show | 36 | HG00140.hp1 HG00438.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.850+236dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625943 | ||||||
chr22:38625943
|
C | CAA | 42 | a0001c0001t0009g0292a0001c0001t0009g0305a0001c0001t0009g0306others(39): Show | 42 | HG00408.hp2 HG00673.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.850+235_850+236dup others(2): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625943 | ||||||
chr22:38625993
|
T | C | 1 | a0001c0001t0042g0145 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.850+187A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625993 | ||||||
chr22:38626060
|
G | A | 2 | a0001c0001t0009g0217a0001c0001t0009g0218 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.850+120C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38626060 | ||||||
chr22:38626156
|
C | A | 2 | a0001c0001t0009g0217a0001c0001t0009g0218 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.850+24G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38626156 | ||||||
chr22:38626174
|
T | G | 1 | a0001c0001t0003g0264 | 1 | HG00733.hp2 | splice_region_variant&intron_variant | LOW | c.850+6A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38626174 | ||||||
chr22:38626548
|
C | A | 3 | a0001c0001t0021g0257a0001c0001t0021g0258a0001c0001t0021g0259 | 3 | HG01346.hp1 HG02451.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.727-245G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626548 | ||||||
chr22:38626796
|
C | T | 1 | a0001c0001t0030g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.727-493G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626796 | ||||||
chr22:38626838
|
A | G | 1 | a0002c0002t0004g0193 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.727-535T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626838 | ||||||
chr22:38626865
|
C | CA | 24 | a0001c0001t0001g0008a0001c0001t0001g0046a0001c0001t0001g0054others(21): Show | 24 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.727-563dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626865 | ||||||
chr22:38626865
|
C | CAA | 17 | a0001c0001t0001g0089a0001c0001t0001g0126a0001c0001t0005g0014others(14): Show | 17 | HG01261.hp1 HG01928.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.727-564_727-563dup others(2): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626865 | ||||||
chr22:38626865
|
CA | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0123a0001c0001t0012g0011others(4): Show | 7 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-563delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626865 | ||||||
chr22:38626882
|
AAAAAAAA others(4): Show |
A | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | NA18971.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.727-590_727-580del others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626882 | ||||||
chr22:38626885
|
A | T | 1 | a0001c0001t0002g0224 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.727-582T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626885 | ||||||
chr22:38626887
|
A | T | 1 | a0001c0001t0002g0224 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.727-584T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626887 | ||||||
chr22:38626889
|
A | AATATATA others(7): Show |
1 | a0001c0003t0013g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.727-587_727-586ins others(14): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626889 | ||||||
chr22:38626889
|
A | ATATATAT others(8): Show |
1 | a0002c0002t0004g0180 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.727-587_727-586ins others(15): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626889 | ||||||
chr22:38626889
|
A | T | 7 | a0001c0001t0001g0139a0001c0001t0002g0224a0001c0001t0014g0163others(4): Show | 7 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.727-586T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626889 | ||||||
chr22:38626891
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0003g0316 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(32): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0002g0249 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0058g0272 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(13): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0003g0320 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.727-589_727-588ins others(19): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAA others(7): Show |
3 | a0001c0001t0002g0247a0001c0001t0003g0221a0001c0001t0017g0288 | 3 | HG00741.hp2 HG01099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.727-589_727-588ins others(14): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(16): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAA others(4): Show |
2 | a0001c0001t0002g0216a0001c0001t0003g0317 | 2 | HG04115.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAA others(6): Show |
3 | a0001c0001t0003g0230a0001c0001t0003g0264a0001c0001t0003g0270 | 3 | HG00733.hp2 HG03654.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(13): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAA others(8): Show |
3 | a0001c0001t0003g0236a0001c0001t0003g0287a0002c0002t0004g0178 | 3 | NA18959.hp1 NA18979.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.727-589_727-588ins others(15): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAA others(5): Show |
13 | a0001c0001t0003g0220a0001c0001t0003g0228a0001c0001t0003g0229others(10): Show | 13 | HG00609.hp1 HG01993.hp2 HG03927.hp1 others(10): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(12): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAA others(7): Show |
5 | a0001c0001t0003g0233a0001c0001t0003g0290a0001c0001t0003g0307others(2): Show | 5 | HG01346.hp1 HG02040.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(14): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAA others(17): Show |
1 | a0002c0002t0004g0204 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(24): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAT | 7 | a0001c0001t0009g0292a0001c0001t0009g0305a0001c0001t0009g0306others(4): Show | 7 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(7): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAT others(4): Show |
5 | a0001c0001t0002g0242a0001c0001t0002g0254a0001c0001t0002g0301others(2): Show | 5 | HG00423.hp2 HG00558.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAT others(6): Show |
7 | a0001c0001t0002g0225a0001c0001t0002g0240a0001c0001t0002g0255others(4): Show | 7 | HG02165.hp2 HG02698.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(13): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAT others(8): Show |
3 | a0001c0001t0002g0291a0002c0002t0004g0200a0002c0002t0015g0209 | 3 | NA18906.hp1 NA18943.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(15): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAT others(10): Show |
2 | a0001c0001t0002g0275a0002c0004t0046g0210 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(17): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAT others(12): Show |
1 | a0002c0002t0004g0185 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.727-589_727-588ins others(19): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAAAT others(16): Show |
2 | a0001c0001t0009g0217a0001c0001t0009g0218 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.727-589_727-588ins others(23): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAATA others(3): Show |
2 | a0001c0001t0016g0294a0001c0001t0053g0253 | 2 | HG02055.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(10): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAATA others(5): Show |
9 | a0001c0001t0002g0244a0001c0001t0003g0231a0001c0001t0003g0237others(6): Show | 9 | HG00280.hp1 HG03041.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(12): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAATA others(7): Show |
3 | a0001c0001t0002g0256a0001c0001t0003g0268a0001c0001t0050g0271 | 3 | HG02155.hp1 HG03688.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(14): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAATA others(9): Show |
2 | a0001c0001t0003g0263a0001c0001t0051g0276 | 2 | HG00642.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.727-589_727-588ins others(16): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAATA others(11): Show |
2 | a0002c0002t0004g0172a0002c0002t0047g0202 | 2 | NA18983.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.727-589_727-588ins others(18): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAATA others(15): Show |
1 | a0002c0002t0004g0214 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.727-589_727-588ins others(22): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAAATA others(17): Show |
1 | a0002c0002t0004g0203 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(24): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAATAT others(4): Show |
13 | a0001c0001t0002g0223a0001c0001t0002g0226a0001c0001t0002g0227others(10): Show | 13 | HG00609.hp2 NA18942.hp2 NA18950.hp2 others(10): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAATAT others(6): Show |
7 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0284others(4): Show | 7 | HG02280.hp2 HG02559.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(13): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAATAT others(8): Show |
2 | a0002c0002t0004g0190a0002c0002t0004g0191 | 2 | HG00673.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(15): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAATAT others(10): Show |
4 | a0001c0001t0002g0274a0002c0002t0004g0211a0002c0002t0025g0194others(1): Show | 4 | HG02922.hp1 NA18960.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(17): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAATAT others(14): Show |
2 | a0002c0002t0004g0213a0002c0002t0011g0199 | 2 | HG03139.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(21): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAAATAT others(16): Show |
1 | a0002c0002t0015g0177 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.727-589_727-588ins others(23): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAATATA others(3): Show |
1 | a0001c0001t0003g0238 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(10): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAATATA others(5): Show |
8 | a0001c0001t0002g0239a0001c0001t0002g0300a0001c0001t0002g0323others(5): Show | 8 | HG02895.hp1 HG02970.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(12): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAATATA others(9): Show |
6 | a0002c0002t0004g0193a0002c0002t0004g0212a0002c0002t0020g0174others(3): Show | 6 | HG02015.hp2 NA18944.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(16): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAATATA others(11): Show |
1 | a0002c0002t0026g0196 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(18): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAAATATA others(15): Show |
1 | a0002c0002t0015g0189 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.727-589_727-588ins others(22): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAATATAT others(4): Show |
2 | a0001c0001t0002g0252a0001c0001t0002g0324 | 2 | HG00558.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.727-589_727-588ins others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAATATAT others(6): Show |
1 | a0001c0001t0027g0302 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(13): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAATATAT others(8): Show |
4 | a0001c0003t0013g0159a0001c0003t0013g0160a0001c0003t0032g0156others(1): Show | 4 | HG00408.hp2 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(15): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AAATATAT others(10): Show |
3 | a0002c0002t0004g0171a0002c0002t0004g0183a0002c0002t0004g0201 | 3 | NA18979.hp2 NA18980.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(17): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AATATATA others(7): Show |
1 | a0002c0002t0004g0184 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.727-602_727-589dup others(14): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AATATATA others(9): Show |
2 | a0002c0002t0004g0181a0002c0002t0004g0182 | 2 | NA19057.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.727-604_727-589dup others(16): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AATATATA others(15): Show |
1 | a0002c0002t0015g0188 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.727-610_727-589dup others(22): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AATATATA others(17): Show |
1 | a0002c0002t0015g0187 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(24): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | AT | 4 | a0001c0001t0001g0121a0001c0001t0001g0128a0001c0001t0001g0151others(1): Show | 4 | HG00140.hp2 HG02056.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(1): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | ATATATAT others(8): Show |
1 | a0001c0003t0013g0158 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(15): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | ATATATAT others(10): Show |
2 | a0001c0007t0013g0157a0002c0002t0026g0195 | 2 | HG02717.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.727-589_727-588ins others(17): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626891
|
A | T | 16 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0123others(13): Show | 16 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.727-588T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | ||||||
chr22:38626892
|
AT | A | 12 | a0001c0001t0001g0006a0001c0001t0001g0049a0001c0001t0001g0072others(9): Show | 13 | HG01175.hp2 HG02015.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.727-590delA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626892 | ||||||
chr22:38626893
|
T | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(86): Show | 91 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.727-590A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626893 | ||||||
chr22:38626895
|
T | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(32): Show | 38 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.727-592A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626895 | ||||||
chr22:38626897
|
T | A | 1 | a0001c0001t0007g0069 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.727-594A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626897 | ||||||
chr22:38626913
|
T | C | 103 | a0001c0001t0002g0216a0001c0001t0002g0219a0001c0001t0002g0223others(100): Show | 103 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.727-610A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626913 | ||||||
chr22:38626913
|
T | TATATATA others(3): Show |
2 | a0001c0001t0002g0004a0001c0001t0002g0297 | 3 | HG03490.hp2 HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.727-611_727-610ins others(10): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626913 | ||||||
chr22:38626938
|
G | T | 2 | a0001c0001t0008g0040a0002c0002t0004g0190 | 2 | HG01243.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.727-635C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626938 | ||||||
chr22:38627053
|
C | T | 5 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(2): Show | 5 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.727-750G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38627053 | ||||||
chr22:38627185
|
C | A | 1 | a0001c0001t0057g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.727-882G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38627185 | ||||||
chr22:38627498
|
T | C | 1 | a0001c0001t0005g0019 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.726+740A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38627498 | ||||||
chr22:38627596
|
G | GT | 11 | a0001c0001t0002g0224a0001c0001t0002g0244a0001c0001t0002g0284others(8): Show | 11 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.726+641dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38627596 | ||||||
chr22:38627698
|
G | A | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.726+540C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38627698 | ||||||
chr22:38627784
|
A | T | 1 | a0001c0001t0003g0238 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.726+454T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38627784 | ||||||
chr22:38628441
|
A | T | 1 | a0001c0001t0002g0284 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.622-99T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 7/16 | chr22 | 38628441 | ||||||
chr22:38628528
|
A | T | 1 | a0001c0001t0045g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.622-186T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 7/16 | chr22 | 38628528 | ||||||
chr22:38628619
|
C | T | 1 | a0002c0004t0046g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.621+215G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 7/16 | chr22 | 38628619 | ||||||
chr22:38628941
|
A | G | 1 | a0001c0001t0009g0309 | 1 | HG02622.hp2 | splice_region_variant&intron_variant | LOW | c.520-6T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38628941 | ||||||
chr22:38628954
|
CAGT | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0057a0001c0001t0001g0062others(3): Show | 6 | NA18943.hp2 NA18951.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-22_520-20delAC others(1): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38628954 | ||||||
chr22:38628956
|
G | T | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(312): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.520-21C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38628956 | ||||||
chr22:38628967
|
G | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0057a0001c0001t0001g0062others(3): Show | 6 | NA18943.hp2 NA18951.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-32C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38628967 | ||||||
chr22:38629272
|
T | C | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.520-337A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629272 | ||||||
chr22:38629290
|
T | C | 2 | a0001c0001t0005g0020a0001c0001t0005g0141 | 2 | HG00735.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.520-355A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629290 | ||||||
chr22:38629336
|
A | G | 1 | a0001c0001t0018g0168 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.520-401T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629336 | ||||||
chr22:38629393
|
C | T | 1 | a0001c0001t0017g0283 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.520-458G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629393 | ||||||
chr22:38629607
|
A | G | 1 | a0001c0001t0030g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.520-672T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629607 | ||||||
chr22:38629620
|
T | C | 1 | a0001c0001t0002g0285 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.520-685A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629620 | ||||||
chr22:38629629
|
G | A | 4 | a0001c0001t0016g0294a0001c0001t0016g0295a0001c0001t0016g0296others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-694C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629629 | ||||||
chr22:38629645
|
G | GACTCACA others(50): Show |
2 | a0001c0001t0001g0058a0001c0001t0001g0071 | 2 | HG00438.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.520-767_520-711dup others(57): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629645 | ||||||
chr22:38629645
|
GACTCACA others(50): Show |
G | 6 | a0001c0003t0013g0158a0001c0003t0013g0159a0001c0003t0013g0160others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-767_520-711del others(57): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629645 | ||||||
chr22:38629754
|
A | G | 1 | a0001c0001t0059g0310 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.520-819T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629754 | ||||||
chr22:38629814
|
A | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0105 | 2 | NA18995.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.520-879T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629814 | ||||||
chr22:38629867
|
T | TA | 157 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.520-933dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629867 | ||||||
chr22:38629890
|
C | T | 2 | a0001c0001t0018g0169a0001c0001t0018g0170 | 2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.520-955G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629890 | ||||||
chr22:38629932
|
A | C | 8 | a0001c0001t0009g0292a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-997T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629932 | ||||||
chr22:38629938
|
C | G | 2 | a0002c0002t0011g0206a0002c0002t0011g0208 | 2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.520-1003G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629938 | ||||||
chr22:38630006
|
T | C | 44 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0228others(41): Show | 44 | HG00423.hp2 HG00609.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.520-1071A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630006 | ||||||
chr22:38630044
|
GCCATCAC others(51): Show |
G | 2 | a0001c0001t0009g0306a0001c0001t0009g0322 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.520-1167_520-1110d others(60): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630044 | ||||||
chr22:38630181
|
C | T | 7 | a0001c0001t0014g0163a0001c0001t0014g0164a0001c0001t0014g0165others(4): Show | 7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.520-1246G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630181 | ||||||
chr22:38630227
|
G | A | 1 | a0001c0001t0010g0059 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.520-1292C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630227 | ||||||
chr22:38630269
|
G | A | 1 | a0001c0001t0002g0250 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.520-1334C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630269 | ||||||
chr22:38630280
|
C | T | 1 | a0002c0002t0011g0173 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.520-1345G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630280 | ||||||
chr22:38630483
|
C | T | 1 | a0001c0001t0043g0073 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.520-1548G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630483 | ||||||
chr22:38630484
|
G | C | 1 | a0001c0001t0008g0035 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.520-1549C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630484 | ||||||
chr22:38630659
|
A | C | 2 | a0002c0002t0004g0171a0002c0002t0026g0195 | 2 | NA18979.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.520-1724T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630659 | ||||||
chr22:38630734
|
C | T | 44 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0228others(41): Show | 44 | HG00423.hp2 HG00609.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.520-1799G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630734 | ||||||
chr22:38630773
|
C | T | 2 | a0001c0001t0005g0005a0001c0001t0005g0031 | 2 | HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.520-1838G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630773 | ||||||
chr22:38630791
|
G | C | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.520-1856C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630791 | ||||||
chr22:38630842
|
C | A | 5 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(2): Show | 5 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.520-1907G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630842 | ||||||
chr22:38630867
|
C | T | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(3): Show | 6 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-1932G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630867 | ||||||
chr22:38630906
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0075 | 2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.520-1971C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630906 | ||||||
chr22:38631107
|
G | A | 1 | a0002c0002t0011g0199 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.520-2172C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38631107 | ||||||
chr22:38631281
|
CAG | C | 136 | a0001c0001t0001g0100a0001c0001t0001g0121a0001c0001t0001g0122others(133): Show | 137 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.520-2348_520-2347d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38631281 | ||||||
chr22:38631325
|
G | A | 1 | a0001c0001t0006g0029 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.520-2390C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38631325 | ||||||
chr22:38631607
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.520-2672C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38631607 | ||||||
chr22:38631629
|
C | T | 4 | a0001c0001t0001g0051a0001c0001t0001g0079a0001c0001t0001g0144others(1): Show | 4 | HG00408.hp1 HG00438.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-2694G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38631629 | ||||||
chr22:38631759
|
CA | C | 7 | a0001c0001t0006g0017a0001c0001t0006g0022a0001c0001t0006g0023others(4): Show | 7 | HG01934.hp2 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.520-2825delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38631759 | ||||||
chr22:38631760
|
AG | A | 7 | a0001c0001t0014g0163a0001c0001t0014g0164a0001c0001t0014g0165others(4): Show | 7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.520-2826delC | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38631760 | ||||||
chr22:38632007
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.520-3072G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632007 | ||||||
chr22:38632089
|
T | C | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.520-3154A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632089 | ||||||
chr22:38632091
|
G | GA | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.520-3157dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632091 | ||||||
chr22:38632135
|
A | C | 2 | a0001c0001t0009g0217a0001c0001t0009g0218 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.520-3200T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632135 | ||||||
chr22:38632178
|
A | C | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.520-3243T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632178 | ||||||
chr22:38632426
|
G | A | 4 | a0001c0001t0008g0033a0001c0001t0008g0035a0001c0001t0008g0036others(1): Show | 4 | HG02055.hp1 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-3491C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632426 | ||||||
chr22:38632427
|
C | T | 8 | a0002c0002t0011g0173a0002c0002t0011g0175a0002c0002t0011g0198others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-3492G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632427 | ||||||
chr22:38632692
|
G | T | 1 | a0002c0002t0011g0198 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520-3757C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632692 | ||||||
chr22:38632817
|
C | T | 5 | a0001c0001t0005g0014a0001c0001t0005g0016a0001c0001t0005g0018others(2): Show | 5 | HG01928.hp2 HG01975.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+3634G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632817 | ||||||
chr22:38632908
|
C | T | 206 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(203): Show | 207 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.519+3543G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632908 | ||||||
chr22:38632984
|
G | A | 2 | a0001c0001t0018g0169a0001c0001t0018g0170 | 2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.519+3467C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632984 | ||||||
chr22:38633306
|
G | GT | 8 | a0001c0001t0009g0292a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.519+3144dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38633306 | ||||||
chr22:38633471
|
A | G | 1 | a0001c0001t0057g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.519+2980T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38633471 | ||||||
chr22:38633647
|
T | C | 1 | a0001c0001t0018g0168 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.519+2804A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38633647 | ||||||
chr22:38633690
|
T | C | 157 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.519+2761A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38633690 | ||||||
chr22:38634199
|
G | T | 5 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(2): Show | 5 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+2252C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634199 | ||||||
chr22:38634200
|
A | T | 5 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(2): Show | 5 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+2251T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634200 | ||||||
chr22:38634221
|
C | CA | 86 | a0001c0001t0001g0121a0001c0001t0001g0146a0001c0001t0002g0004others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.519+2229dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634221 | ||||||
chr22:38634221
|
C | CAA | 18 | a0001c0001t0002g0225a0001c0001t0002g0226a0001c0001t0002g0246others(15): Show | 18 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.519+2228_519+2229d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634221 | ||||||
chr22:38634221
|
CA | C | 47 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0048others(44): Show | 47 | HG00408.hp2 HG00673.hp2 HG01515.hp2 others(44): Show |
intron_variant | MODIFIER | c.519+2229delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634221 | ||||||
chr22:38634254
|
TAG | T | 4 | a0001c0003t0013g0158a0001c0003t0013g0159a0001c0003t0013g0161others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+2195_519+2196d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634254 | ||||||
chr22:38634396
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.519+2055A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634396 | ||||||
chr22:38634410
|
T | G | 1 | a0001c0001t0001g0120 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.519+2041A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634410 | ||||||
chr22:38634851
|
G | A | 6 | a0001c0003t0013g0158a0001c0003t0013g0159a0001c0003t0013g0160others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+1600C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634851 | ||||||
chr22:38634894
|
T | C | 6 | a0001c0001t0012g0011a0001c0001t0012g0113a0001c0001t0012g0114others(3): Show | 6 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.519+1557A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634894 | ||||||
chr22:38634947
|
A | G | 10 | a0001c0001t0006g0017a0001c0001t0006g0022a0001c0001t0006g0023others(7): Show | 10 | HG01934.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.519+1504T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634947 | ||||||
chr22:38635157
|
C | T | 2 | a0001c0001t0009g0217a0001c0001t0009g0218 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.519+1294G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635157 | ||||||
chr22:38635181
|
G | A | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.519+1270C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635181 | ||||||
chr22:38635182
|
C | T | 1 | a0001c0001t0028g0074 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.519+1269G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635182 | ||||||
chr22:38635190
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.519+1261G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635190 | ||||||
chr22:38635228
|
C | CA | 20 | a0001c0001t0001g0062a0001c0001t0001g0067a0001c0001t0001g0086others(17): Show | 20 | HG01433.hp2 HG01934.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.519+1222dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635228 | ||||||
chr22:38635228
|
CA | C | 157 | a0001c0001t0001g0123a0001c0001t0001g0144a0001c0001t0001g0147others(154): Show | 158 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.519+1222delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635228 | ||||||
chr22:38635657
|
A | G | 1 | a0001c0001t0003g0233 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.519+794T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635657 | ||||||
chr22:38635894
|
G | C | 7 | a0001c0001t0003g0232a0001c0001t0003g0235a0001c0001t0003g0237others(4): Show | 7 | NA18939.hp1 NA18961.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+557C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635894 | ||||||
chr22:38635896
|
C | T | 6 | a0001c0003t0013g0158a0001c0003t0013g0159a0001c0003t0013g0160others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+555G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635896 | ||||||
chr22:38636055
|
GGAAA | G | 7 | a0001c0001t0003g0232a0001c0001t0003g0235a0001c0001t0003g0237others(4): Show | 7 | NA18939.hp1 NA18961.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+392_519+395del others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38636055 | ||||||
chr22:38636107
|
C | CAGAAA | 139 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(136): Show | 140 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.519+339_519+343dup others(5): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38636107 | ||||||
chr22:38636122
|
A | AAG | 46 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170others(43): Show | 46 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(43): Show |
intron_variant | MODIFIER | c.519+328_519+329ins others(2): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38636122 | ||||||
chr22:38636126
|
G | A | 46 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170others(43): Show | 46 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(43): Show |
intron_variant | MODIFIER | c.519+325C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38636126 | ||||||
chr22:38636160
|
T | C | 6 | a0002c0002t0004g0172a0002c0002t0004g0185a0002c0002t0004g0201others(3): Show | 6 | NA18983.hp2 NA18994.hp2 NA19012.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+291A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38636160 | ||||||
chr22:38636247
|
T | C | 1 | a0001c0001t0002g0301 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.519+204A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38636247 | ||||||
chr22:38636265
|
C | T | 240 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0001g0118others(237): Show | 242 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.519+186G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38636265 | ||||||
chr22:38636343
|
C | T | 55 | a0001c0001t0002g0219a0001c0001t0002g0274a0001c0001t0002g0275others(52): Show | 55 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.519+108G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38636343 | ||||||
chr22:38636671
|
C | T | 3 | a0001c0001t0003g0228a0001c0001t0003g0281a0001c0001t0003g0282 | 3 | HG00609.hp1 NA18951.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.373-74G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636671 | ||||||
chr22:38636685
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.373-88G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636685 | ||||||
chr22:38636728
|
T | C | 1 | a0001c0001t0001g0003 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.373-131A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636728 | ||||||
chr22:38636766
|
ATTTCT | A | 35 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(32): Show | 35 | HG00408.hp2 HG00673.hp2 HG02015.hp2 others(32): Show |
intron_variant | MODIFIER | c.373-174_373-170del others(5): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636766 | ||||||
chr22:38636766
|
ATTTCTT | A | 10 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170others(7): Show | 10 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.373-175_373-170del others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636766 | ||||||
chr22:38636770
|
CT | C | 112 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0044others(109): Show | 113 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.373-174delA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636770 | ||||||
chr22:38636774
|
T | A | 3 | a0002c0002t0020g0174a0002c0002t0020g0186a0002c0002t0020g0197 | 3 | NA18944.hp1 NA18964.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.373-177A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636774 | ||||||
chr22:38636775
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.373-178A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636775 | ||||||
chr22:38636920
|
G | A | 1 | a0001c0001t0009g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.373-323C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636920 | ||||||
chr22:38637043
|
G | T | 1 | a0001c0001t0001g0215 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.373-446C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38637043 | ||||||
chr22:38637115
|
A | G | 4 | a0001c0001t0002g0240a0001c0001t0002g0254a0001c0001t0002g0284others(1): Show | 4 | HG00558.hp1 NA18942.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-518T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38637115 | ||||||
chr22:38637193
|
G | A | 1 | a0001c0001t0027g0302 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.373-596C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38637193 | ||||||
chr22:38637306
|
T | C | 1 | a0001c0001t0018g0168 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.373-709A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38637306 | ||||||
chr22:38637613
|
C | A | 2 | a0001c0001t0018g0169a0001c0001t0018g0170 | 2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.373-1016G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38637613 | ||||||
chr22:38637663
|
G | A | 1 | a0001c0001t0053g0253 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.373-1066C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38637663 | ||||||
chr22:38637969
|
C | T | 4 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0323others(1): Show | 4 | HG02280.hp2 HG02895.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.372+777G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38637969 | ||||||
chr22:38638670
|
C | G | 1 | a0001c0001t0018g0168 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.372+76G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38638670 | ||||||
chr22:38638862
|
G | A | 96 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(93): Show | 97 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.296-40C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 4/16 | chr22 | 38638862 | ||||||
chr22:38639408
|
C | CG | 49 | a0001c0001t0003g0228a0001c0001t0003g0232a0001c0001t0003g0233others(46): Show | 49 | HG00408.hp2 HG01243.hp2 HG01891.hp2 others(46): Show |
intron_variant | MODIFIER | c.295+246dupC | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 4/16 | chr22 | 38639408 | ||||||
chr22:38639409
|
G | GA | 6 | a0001c0001t0001g0065a0001c0001t0001g0089a0001c0001t0018g0169others(3): Show | 6 | HG02027.hp2 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.295+245dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 4/16 | chr22 | 38639409 | ||||||
chr22:38639409
|
GA | G | 41 | a0001c0001t0001g0010a0001c0001t0001g0122a0001c0001t0003g0236others(38): Show | 41 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.295+245delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 4/16 | chr22 | 38639409 | ||||||
chr22:38639410
|
A | G | 86 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+245T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 4/16 | chr22 | 38639410 | ||||||
chr22:38639411
|
A | G | 3 | a0001c0001t0002g0315a0001c0001t0003g0236a0001c0001t0003g0307 | 3 | NA18979.hp1 NA19068.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.295+244T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 4/16 | chr22 | 38639411 | ||||||
chr22:38639462
|
T | C | 4 | a0002c0002t0011g0173a0002c0002t0011g0198a0002c0002t0011g0205others(1): Show | 4 | HG02145.hp1 HG03453.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.295+193A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 4/16 | chr22 | 38639462 | ||||||
chr22:38639574
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.295+81C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 4/16 | chr22 | 38639574 | ||||||
chr22:38639755
|
G | A | 6 | a0001c0001t0014g0163a0001c0001t0014g0164a0001c0001t0014g0165others(3): Show | 6 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.226-31C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38639755 | ||||||
chr22:38639848
|
G | C | 2 | a0002c0002t0011g0206a0002c0002t0011g0208 | 2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.226-124C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38639848 | ||||||
chr22:38640137
|
C | A | 1 | a0001c0001t0003g0290 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.226-413G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38640137 | ||||||
chr22:38640263
|
G | A | 2 | a0001c0001t0009g0217a0001c0001t0009g0218 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.226-539C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38640263 | ||||||
chr22:38640275
|
T | C | 157 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.226-551A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38640275 | ||||||
chr22:38640293
|
A | G | 1 | a0001c0001t0005g0014 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.226-569T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38640293 | ||||||
chr22:38640324
|
C | T | 23 | a0001c0001t0005g0005a0001c0001t0005g0014a0001c0001t0005g0016others(20): Show | 23 | HG00735.hp1 HG01261.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.226-600G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38640324 | ||||||
chr22:38640455
|
A | C | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.226-731T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38640455 | ||||||
chr22:38640764
|
T | C | 157 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.226-1040A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38640764 | ||||||
chr22:38640927
|
G | T | 1 | a0001c0001t0037g0130 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.226-1203C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38640927 | ||||||
chr22:38641125
|
GGA | G | 157 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.226-1403_226-1402d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641125 | ||||||
chr22:38641422
|
C | T | 1 | a0001c0001t0003g0289 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.226-1698G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641422 | ||||||
chr22:38641512
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.226-1788A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641512 | ||||||
chr22:38641547
|
A | G | 205 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(202): Show | 206 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.226-1823T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641547 | ||||||
chr22:38641551
|
C | CA | 10 | a0001c0001t0001g0062a0001c0001t0001g0075a0001c0001t0001g0078others(7): Show | 10 | HG00741.hp1 HG02015.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.226-1828dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641551 | ||||||
chr22:38641551
|
CA | C | 200 | a0001c0001t0001g0091a0001c0001t0002g0004a0001c0001t0002g0216others(197): Show | 201 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.226-1828delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641551 | ||||||
chr22:38641559
|
A | C | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.226-1835T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641559 | ||||||
chr22:38641564
|
A | C | 47 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170others(44): Show | 47 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.226-1840T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641564 | ||||||
chr22:38641699
|
T | TGTTG | 157 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.226-1979_226-1976d others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641699 | ||||||
chr22:38641868
|
C | T | 4 | a0001c0001t0016g0294a0001c0001t0016g0295a0001c0001t0016g0296others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-2144G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641868 | ||||||
chr22:38641917
|
C | G | 2 | a0001c0001t0019g0135a0001c0001t0019g0136 | 2 | HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.226-2193G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641917 | ||||||
chr22:38641948
|
G | GAT | 23 | a0001c0001t0002g0324a0001c0001t0018g0169a0001c0001t0018g0170others(20): Show | 23 | HG00408.hp2 HG00673.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.226-2225_226-2224i others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641948 | ||||||
chr22:38641948
|
G | GATGT | 15 | a0002c0002t0004g0172a0002c0002t0004g0180a0002c0002t0004g0181others(12): Show | 15 | NA18952.hp2 NA18962.hp1 NA18980.hp1 others(12): Show |
intron_variant | MODIFIER | c.226-2225_226-2224i others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641948 | ||||||
chr22:38641948
|
G | GGT | 63 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(60): Show | 65 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.226-2226_226-2225d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641948 | ||||||
chr22:38641948
|
G | GGTGT | 12 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0053others(9): Show | 12 | HG00423.hp1 HG01167.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.226-2228_226-2225d others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641948 | ||||||
chr22:38641948
|
G | GGTGTGT | 5 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(2): Show | 5 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-2230_226-2225d others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641948 | ||||||
chr22:38641948
|
GGT | G | 18 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0001t0002g0244others(15): Show | 18 | HG00609.hp1 HG02135.hp2 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.226-2226_226-2225d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641948 | ||||||
chr22:38641948
|
GGTGTGTG others(7): Show |
G | 6 | a0001c0003t0013g0158a0001c0003t0013g0159a0001c0003t0013g0160others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-2238_226-2225d others(16): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641948 | ||||||
chr22:38641949
|
G | A | 100 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(97): Show | 101 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.226-2225C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641949 | ||||||
chr22:38641951
|
G | A | 18 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0001t0002g0244others(15): Show | 18 | HG00609.hp1 HG02135.hp2 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.226-2227C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641951 | ||||||
chr22:38641957
|
G | A | 1 | a0001c0001t0018g0168 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.226-2233C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641957 | ||||||
chr22:38641964
|
TGTGTGTG others(9): Show |
T | 1 | a0001c0001t0001g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.226-2256_226-2241d others(18): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641964 | ||||||
chr22:38641972
|
T | C | 4 | a0001c0001t0002g0226a0001c0001t0002g0299a0001c0001t0002g0315others(1): Show | 4 | HG00642.hp1 HG02280.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-2248A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641972 | ||||||
chr22:38641974
|
T | C | 115 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(112): Show | 116 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.226-2250A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641974 | ||||||
chr22:38641974
|
T | TGC | 28 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0121others(25): Show | 28 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.226-2252_226-2251d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641974 | ||||||
chr22:38641974
|
T | TGTGC | 18 | a0001c0001t0001g0094a0001c0001t0001g0139a0001c0001t0005g0005others(15): Show | 18 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.226-2251_226-2250i others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641974 | ||||||
chr22:38641974
|
T | TGTGTGC | 11 | a0001c0001t0005g0014a0001c0001t0005g0018a0001c0001t0005g0019others(8): Show | 11 | HG00735.hp1 HG01261.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.226-2251_226-2250i others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641974 | ||||||
chr22:38641976
|
CGCACGTG others(5): Show |
C | 8 | a0001c0001t0009g0292a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-2264_226-2253d others(14): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641976 | ||||||
chr22:38641979
|
A | G | 185 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(182): Show | 186 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.226-2255T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641979 | ||||||
chr22:38642044
|
C | T | 4 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0323others(1): Show | 4 | HG02280.hp2 HG02895.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-2320G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642044 | ||||||
chr22:38642141
|
A | G | 1 | a0001c0001t0053g0253 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.226-2417T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642141 | ||||||
chr22:38642152
|
C | T | 1 | a0001c0001t0041g0052 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.226-2428G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642152 | ||||||
chr22:38642263
|
T | C | 1 | a0001c0001t0038g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.226-2539A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642263 | ||||||
chr22:38642341
|
C | T | 6 | a0001c0001t0003g0228a0001c0001t0003g0279a0001c0001t0003g0280others(3): Show | 6 | HG00609.hp1 NA18951.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.226-2617G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642341 | ||||||
chr22:38642705
|
G | T | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.225+2858C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642705 | ||||||
chr22:38642785
|
A | C | 106 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(103): Show | 107 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.225+2778T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642785 | ||||||
chr22:38642791
|
T | C | 193 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(190): Show | 194 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.225+2772A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642791 | ||||||
chr22:38642993
|
T | C | 43 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(40): Show | 43 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.225+2570A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642993 | ||||||
chr22:38643036
|
T | A | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.225+2527A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643036 | ||||||
chr22:38643159
|
A | G | 4 | a0002c0002t0004g0180a0002c0002t0004g0181a0002c0002t0004g0211others(1): Show | 4 | NA18962.hp1 NA18982.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+2404T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643159 | ||||||
chr22:38643181
|
T | C | 4 | a0001c0001t0008g0033a0001c0001t0008g0035a0001c0001t0008g0036others(1): Show | 4 | HG02055.hp1 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+2382A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643181 | ||||||
chr22:38643201
|
A | G | 6 | a0001c0001t0005g0005a0001c0001t0005g0020a0001c0001t0005g0031others(3): Show | 6 | HG00735.hp1 HG01261.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+2362T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643201 | ||||||
chr22:38643315
|
C | CA | 43 | a0001c0001t0037g0130a0002c0002t0004g0171a0002c0002t0004g0172others(40): Show | 43 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.225+2247dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643315 | ||||||
chr22:38643328
|
ATAG | A | 4 | a0001c0001t0002g0004a0001c0001t0002g0297a0001c0001t0009g0217others(1): Show | 5 | HG02896.hp1 HG02897.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+2232_225+2234d others(5): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643328 | ||||||
chr22:38643329
|
TAGTG | T | 107 | a0001c0001t0001g0075a0001c0001t0002g0216a0001c0001t0002g0219others(104): Show | 107 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.225+2230_225+2233d others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643329 | ||||||
chr22:38643332
|
T | A | 4 | a0001c0001t0002g0004a0001c0001t0002g0297a0001c0001t0009g0217others(1): Show | 5 | HG02896.hp1 HG02897.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+2231A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643332 | ||||||
chr22:38643333
|
G | T | 4 | a0001c0001t0002g0004a0001c0001t0002g0297a0001c0001t0009g0217others(1): Show | 5 | HG02896.hp1 HG02897.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+2230C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643333 | ||||||
chr22:38643400
|
C | T | 4 | a0001c0001t0003g0220a0001c0001t0003g0229a0001c0001t0003g0230others(1): Show | 4 | NA18983.hp1 NA19012.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+2163G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643400 | ||||||
chr22:38643449
|
G | C | 6 | a0001c0001t0005g0014a0001c0001t0005g0016a0001c0001t0005g0018others(3): Show | 6 | HG01928.hp2 HG01975.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+2114C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643449 | ||||||
chr22:38643465
|
G | A | 7 | a0001c0001t0001g0067a0001c0001t0001g0103a0001c0001t0001g0104others(4): Show | 7 | HG02165.hp1 HG04184.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+2098C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643465 | ||||||
chr22:38643615
|
T | A | 2 | a0001c0001t0009g0312a0001c0001t0009g0313 | 2 | HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.225+1948A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643615 | ||||||
chr22:38643704
|
C | T | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.225+1859G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643704 | ||||||
chr22:38643850
|
G | C | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.225+1713C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643850 | ||||||
chr22:38643962
|
A | G | 4 | a0001c0001t0008g0033a0001c0001t0008g0035a0001c0001t0008g0036others(1): Show | 4 | HG02055.hp1 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+1601T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643962 | ||||||
chr22:38644008
|
G | A | 4 | a0001c0001t0016g0294a0001c0001t0016g0295a0001c0001t0016g0296others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+1555C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644008 | ||||||
chr22:38644015
|
C | T | 1 | a0001c0001t0002g0239 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.225+1548G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644015 | ||||||
chr22:38644019
|
C | T | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.225+1544G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644019 | ||||||
chr22:38644038
|
C | T | 5 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(2): Show | 5 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+1525G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644038 | ||||||
chr22:38644095
|
G | A | 1 | a0001c0001t0018g0168 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.225+1468C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644095 | ||||||
chr22:38644145
|
C | CA | 58 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0068others(55): Show | 58 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.225+1417dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644145 | ||||||
chr22:38644145
|
C | CAA | 33 | a0002c0002t0004g0172a0002c0002t0004g0178a0002c0002t0004g0190others(30): Show | 33 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.225+1416_225+1417d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644145 | ||||||
chr22:38644145
|
CA | C | 11 | a0001c0001t0001g0051a0001c0001t0002g0246a0001c0001t0003g0261others(8): Show | 11 | HG00408.hp1 HG00733.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.225+1417delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644145 | ||||||
chr22:38644145
|
CAAAAAAA | C | 6 | a0002c0002t0004g0180a0002c0002t0004g0181a0002c0002t0004g0182others(3): Show | 6 | NA18962.hp1 NA18980.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+1411_225+1417d others(9): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644145 | ||||||
chr22:38644274
|
G | A | 170 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(167): Show | 171 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.225+1289C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644274 | ||||||
chr22:38644315
|
A | AAAAGAGG others(78): Show |
6 | a0001c0001t0001g0072a0001c0001t0005g0014a0001c0001t0005g0016others(3): Show | 6 | HG01928.hp2 HG01975.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+1163_225+1247d others(87): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | ||||||
chr22:38644315
|
A | AAAAGAGG others(4328): Show |
2 | a0001c0001t0003g0282a0001c0001t0003g0319 | 2 | HG00609.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.225+1247_225+1248i others(4337): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | ||||||
chr22:38644315
|
A | AAAAGAGG others(4328): Show |
1 | a0001c0001t0003g0279 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.225+1247_225+1248i others(4337): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | ||||||
chr22:38644315
|
A | AAAAGAGG others(4243): Show |
1 | a0001c0001t0003g0280 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.225+1247_225+1248i others(4252): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | ||||||
chr22:38644315
|
A | AAAAGAGG others(1608): Show |
1 | a0001c0001t0002g0252 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.225+1247_225+1248i others(1617): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | ||||||
chr22:38644315
|
A | AAAAGAGG others(3053): Show |
1 | a0001c0001t0002g0234 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.225+1247_225+1248i others(3062): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | ||||||
chr22:38644315
|
A | AAAAGAGG others(4838): Show |
1 | a0001c0001t0002g0251 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.225+1247_225+1248i others(4847): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | ||||||
chr22:38644315
|
A | AAAAGAGG others(2033): Show |
1 | a0001c0001t0002g0324 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.225+1247_225+1248i others(2042): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | ||||||
chr22:38644315
|
AAAAGAGG others(78): Show |
A | 3 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0044g0143 | 3 | HG02056.hp2 NA19002.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.225+1163_225+1247d others(87): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | ||||||
chr22:38644337
|
A | ACAGAGGA others(78): Show |
2 | a0001c0001t0018g0169a0001c0001t0018g0170 | 2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.225+1225_225+1226i others(87): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644337 | ||||||
chr22:38644337
|
A | ACAGAGGA others(4413): Show |
1 | a0001c0001t0003g0281 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.225+1225_225+1226i others(4422): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644337 | ||||||
chr22:38644337
|
A | G | 110 | a0001c0001t0001g0071a0001c0001t0002g0004a0001c0001t0002g0216others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.225+1226T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644337 | ||||||
chr22:38644341
|
AGGACTGT others(3): Show |
A | 43 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(40): Show | 43 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.225+1212_225+1221d others(12): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644341 | ||||||
chr22:38644370
|
T | C | 94 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(91): Show | 95 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.225+1193A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644370 | ||||||
chr22:38644370
|
T | CGTGACAC others(3562): Show |
1 | a0001c0001t0009g0218 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.225+1193_225+1194i others(3571): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644370 | ||||||
chr22:38644370
|
T | CGTGACAC others(3563): Show |
1 | a0001c0001t0009g0217 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.225+1193_225+1194i others(3572): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644370 | ||||||
chr22:38644370
|
T | CGTGACAC others(6368): Show |
2 | a0001c0001t0003g0266a0001c0001t0003g0303 | 2 | NA18942.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.225+1193_225+1194i others(6377): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644370 | ||||||
chr22:38644370
|
T | CGTGACAC others(5093): Show |
1 | a0001c0001t0017g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.225+1193_225+1194i others(5102): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644370 | ||||||
chr22:38644395
|
G | A | 3 | a0001c0001t0017g0277a0001c0001t0017g0283a0001c0001t0051g0276 | 3 | HG00280.hp1 HG00642.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.225+1168C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644395 | ||||||
chr22:38644404
|
G | C | 1 | a0001c0001t0002g0249 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.225+1159C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644404 | ||||||
chr22:38644415
|
G | C | 1 | a0001c0001t0001g0112 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.225+1148C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644415 | ||||||
chr22:38644422
|
A | G | 112 | a0001c0001t0001g0070a0001c0001t0001g0134a0001c0001t0002g0004others(109): Show | 113 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.225+1141T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644422 | ||||||
chr22:38644423
|
C | AAGAGGAC others(4328): Show |
1 | a0001c0001t0003g0228 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.225+1140_225+1141i others(4337): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644423 | ||||||
chr22:38644446
|
A | ACTATGCT others(3567): Show |
1 | a0001c0001t0003g0237 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(3576): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(3053): Show |
1 | a0001c0001t0051g0276 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(3062): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4668): Show |
1 | a0001c0001t0057g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4677): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4838): Show |
1 | a0001c0001t0002g0300 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4847): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(5960): Show |
1 | a0001c0001t0003g0232 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5969): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(5943): Show |
1 | a0001c0001t0003g0267 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5952): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(3138): Show |
1 | a0001c0001t0055g0243 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(3147): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(5263): Show |
1 | a0001c0001t0002g0249 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5272): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(3053): Show |
2 | a0001c0001t0002g0244a0001c0001t0022g0245 | 2 | HG03927.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.225+1116_225+1117i others(3062): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4923): Show |
1 | a0001c0001t0002g0254 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4932): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4753): Show |
1 | a0001c0001t0002g0255 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4762): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4413): Show |
1 | a0001c0001t0002g0297 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4422): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4413): Show |
1 | a0001c0001t0002g0004 | 2 | HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.225+1116_225+1117i others(4422): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4923): Show |
1 | a0001c0001t0002g0239 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4932): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(2373): Show |
7 | a0001c0001t0009g0292a0001c0001t0009g0305a0001c0001t0009g0306others(4): Show | 7 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+1116_225+1117i others(2382): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(2373): Show |
1 | a0001c0001t0009g0309 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(2382): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4835): Show |
2 | a0001c0001t0016g0294a0001c0001t0016g0296 | 2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.225+1116_225+1117i others(4844): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6453): Show |
1 | a0001c0001t0003g0320 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6462): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(3138): Show |
1 | a0001c0001t0002g0308 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(3147): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(3053): Show |
9 | a0001c0001t0002g0224a0001c0001t0002g0225a0001c0001t0002g0226others(6): Show | 9 | HG01099.hp1 HG02027.hp1 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.225+1116_225+1117i others(3062): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(3053): Show |
1 | a0001c0001t0002g0223 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(3062): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4923): Show |
1 | a0001c0001t0002g0299 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4932): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(5008): Show |
1 | a0001c0001t0056g0304 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5017): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4923): Show |
1 | a0001c0001t0002g0323 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4932): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4838): Show |
1 | a0001c0001t0002g0240 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4847): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6538): Show |
1 | a0001c0001t0003g0229 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6547): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(5008): Show |
1 | a0001c0001t0053g0253 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5017): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(5688): Show |
1 | a0001c0001t0002g0284 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5697): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4838): Show |
1 | a0001c0001t0002g0285 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4847): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4921): Show |
1 | a0001c0001t0002g0315 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4930): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4838): Show |
2 | a0001c0001t0002g0241a0001c0001t0054g0321 | 2 | NA19009.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.225+1116_225+1117i others(4847): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4750): Show |
1 | a0001c0001t0016g0311 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4759): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(5603): Show |
1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5612): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(5688): Show |
1 | a0001c0001t0002g0275 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5697): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4923): Show |
1 | a0001c0001t0002g0301 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4932): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4838): Show |
1 | a0001c0001t0002g0250 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4847): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4838): Show |
1 | a0001c0001t0002g0256 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4847): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4923): Show |
1 | a0001c0001t0002g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4932): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6198): Show |
1 | a0001c0001t0002g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6207): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(3393): Show |
2 | a0001c0001t0003g0289a0001c0001t0003g0290 | 2 | HG02040.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.225+1116_225+1117i others(3402): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(5603): Show |
1 | a0001c0001t0002g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5612): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6368): Show |
2 | a0001c0001t0003g0236a0001c0001t0003g0307 | 2 | NA18979.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.225+1116_225+1117i others(6377): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6368): Show |
3 | a0001c0001t0017g0288a0001c0001t0050g0271a0001c0001t0058g0272 | 3 | HG01433.hp1 HG02135.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.225+1116_225+1117i others(6377): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6453): Show |
1 | a0001c0001t0003g0262 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6462): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6368): Show |
6 | a0001c0001t0003g0220a0001c0001t0003g0230a0001c0001t0003g0231others(3): Show | 6 | NA18959.hp1 NA18980.hp2 NA19012.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+1116_225+1117i others(6377): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6113): Show |
1 | a0001c0001t0003g0316 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6122): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(5603): Show |
1 | a0001c0001t0052g0286 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5612): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6368): Show |
2 | a0001c0001t0003g0221a0001c0001t0003g0268 | 2 | HG00741.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.225+1116_225+1117i others(6377): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(5858): Show |
1 | a0001c0001t0003g0235 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5867): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6368): Show |
1 | a0001c0001t0003g0270 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6377): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6368): Show |
1 | a0001c0001t0003g0317 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6377): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6368): Show |
1 | a0001c0001t0027g0265 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6377): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4668): Show |
1 | a0001c0001t0003g0260 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4677): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6538): Show |
1 | a0001c0001t0021g0257 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6547): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6538): Show |
1 | a0001c0001t0021g0259 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6547): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(5943): Show |
1 | a0001c0001t0003g0269 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5952): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(5858): Show |
1 | a0001c0001t0003g0273 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5867): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4583): Show |
1 | a0001c0001t0002g0242 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4592): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(5775): Show |
1 | a0001c0001t0017g0277 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5784): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6198): Show |
1 | a0001c0001t0003g0238 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6207): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4413): Show |
1 | a0001c0001t0003g0261 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4422): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6453): Show |
1 | a0001c0001t0017g0283 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6462): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6453): Show |
1 | a0001c0001t0021g0258 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6462): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(5858): Show |
1 | a0001c0001t0003g0293 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5867): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6573): Show |
1 | a0001c0001t0003g0264 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6582): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6198): Show |
1 | a0001c0001t0003g0263 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6207): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(4835): Show |
1 | a0001c0001t0016g0295 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4844): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | ACTATGCT others(6538): Show |
1 | a0001c0001t0027g0302 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6547): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644446
|
A | C | 7 | a0001c0001t0002g0234a0001c0001t0002g0251a0001c0001t0002g0252others(4): Show | 7 | HG00558.hp2 NA18942.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+1117T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | ||||||
chr22:38644455
|
T | C | 6 | a0001c0001t0003g0228a0001c0001t0003g0279a0001c0001t0003g0280others(3): Show | 6 | HG00609.hp1 NA18951.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+1108A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644455 | ||||||
chr22:38644462
|
C | G | 4 | a0001c0001t0002g0240a0001c0001t0021g0257a0001c0001t0021g0258others(1): Show | 4 | HG01346.hp1 HG02451.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+1101G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644462 | ||||||
chr22:38644507
|
A | ACAGAGGA others(78): Show |
2 | a0001c0001t0001g0070a0001c0001t0001g0134 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.225+1055_225+1056i others(87): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644507 | ||||||
chr22:38644507
|
A | G | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.225+1056T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644507 | ||||||
chr22:38644520
|
G | A | 47 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170others(44): Show | 47 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.225+1043C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644520 | ||||||
chr22:38644527
|
C | T | 2 | a0001c0001t0003g0260a0001c0001t0003g0261 | 2 | HG01074.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.225+1036G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644527 | ||||||
chr22:38644532
|
C | G | 1 | a0001c0001t0002g0239 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.225+1031G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644532 | ||||||
chr22:38644583
|
T | A | 4 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0323others(1): Show | 4 | HG02280.hp2 HG02895.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+980A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644583 | ||||||
chr22:38644591
|
T | C | 10 | a0001c0001t0006g0017a0001c0001t0006g0022a0001c0001t0006g0023others(7): Show | 10 | HG01934.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.225+972A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644591 | ||||||
chr22:38644593
|
TACA | T | 106 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(103): Show | 107 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.225+967_225+969del others(3): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644593 | ||||||
chr22:38644597
|
A | C | 47 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170others(44): Show | 47 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.225+966T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644597 | ||||||
chr22:38644612
|
T | G | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.225+951A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644612 | ||||||
chr22:38644728
|
G | A | 107 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(104): Show | 108 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.225+835C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644728 | ||||||
chr22:38644758
|
T | C | 6 | a0001c0003t0013g0158a0001c0003t0013g0159a0001c0003t0013g0160others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+805A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644758 | ||||||
chr22:38644809
|
C | T | 4 | a0001c0001t0008g0033a0001c0001t0008g0035a0001c0001t0008g0036others(1): Show | 4 | HG02055.hp1 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+754G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644809 | ||||||
chr22:38644810
|
G | A | 1 | a0001c0001t0002g0256 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.225+753C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644810 | ||||||
chr22:38644820
|
G | A | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.225+743C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644820 | ||||||
chr22:38644840
|
C | G | 36 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0223others(33): Show | 37 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.225+723G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644840 | ||||||
chr22:38644885
|
T | C | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.225+678A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644885 | ||||||
chr22:38645019
|
G | T | 1 | a0001c0001t0006g0030 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.225+544C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645019 | ||||||
chr22:38645030
|
T | C | 6 | a0001c0001t0012g0011a0001c0001t0012g0113a0001c0001t0012g0114others(3): Show | 6 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+533A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645030 | ||||||
chr22:38645036
|
A | G | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.225+527T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645036 | ||||||
chr22:38645080
|
T | C | 1 | a0001c0001t0006g0030 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.225+483A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645080 | ||||||
chr22:38645087
|
AAAAT | A | 112 | a0001c0001t0001g0118a0001c0001t0002g0004a0001c0001t0002g0216others(109): Show | 113 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.225+472_225+475del others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645087 | ||||||
chr22:38645087
|
AAAATAAA others(1): Show |
A | 43 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(40): Show | 43 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.225+468_225+475del others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645087 | ||||||
chr22:38645141
|
T | C | 1 | a0001c0001t0007g0069 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.225+422A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645141 | ||||||
chr22:38645252
|
A | G | 4 | a0001c0001t0016g0294a0001c0001t0016g0295a0001c0001t0016g0296others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+311T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645252 | ||||||
chr22:38645284
|
G | A | 2 | a0001c0001t0003g0320a0001c0001t0017g0283 | 2 | HG00280.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.225+279C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645284 | ||||||
chr22:38645483
|
AGGGCACT others(21): Show |
A | 2 | a0001c0001t0005g0005a0001c0001t0005g0031 | 2 | HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.225+52_225+79delCG others(26): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645483 | ||||||
chr22:38645783
|
ATTTC | A | 4 | a0001c0001t0005g0141a0001c0001t0018g0168a0001c0001t0018g0169others(1): Show | 4 | HG00735.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-142_143-139del others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38645783 | ||||||
chr22:38646209
|
C | G | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.143-564G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646209 | ||||||
chr22:38646214
|
C | G | 47 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170others(44): Show | 47 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.143-569G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646214 | ||||||
chr22:38646216
|
G | T | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.143-571C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646216 | ||||||
chr22:38646248
|
C | CT | 28 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0015others(25): Show | 28 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.143-604dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646248 | ||||||
chr22:38646248
|
C | CTTTTT | 10 | a0001c0001t0008g0041a0001c0001t0014g0165a0001c0001t0014g0166others(7): Show | 10 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-608_143-604dup others(5): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646248 | ||||||
chr22:38646248
|
C | CTTTTTTT | 6 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0014g0163others(3): Show | 6 | HG01243.hp2 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-610_143-604dup others(7): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646248 | ||||||
chr22:38646248
|
CTTTTTTT | C | 12 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0002g0216others(9): Show | 12 | HG02055.hp2 HG02129.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.143-610_143-604del others(7): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646248 | ||||||
chr22:38646248
|
CTTTTTTT others(1): Show |
C | 118 | a0001c0001t0002g0004a0001c0001t0002g0219a0001c0001t0002g0223others(115): Show | 119 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.143-611_143-604del others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646248 | ||||||
chr22:38646248
|
CTTTTTTT others(2): Show |
C | 9 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0001t0003g0293others(6): Show | 9 | HG02897.hp1 HG03516.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-612_143-604del others(9): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646248 | ||||||
chr22:38646248
|
CTTTTTTT others(3): Show |
C | 39 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0180others(36): Show | 39 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.143-613_143-604del others(10): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646248 | ||||||
chr22:38646248
|
CTTTTTTT others(4): Show |
C | 1 | a0002c0004t0046g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.143-614_143-604del others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646248 | ||||||
chr22:38646292
|
C | T | 1 | a0001c0001t0018g0168 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.143-647G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646292 | ||||||
chr22:38646299
|
G | A | 2 | a0001c0001t0005g0005a0001c0001t0005g0031 | 2 | HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.143-654C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646299 | ||||||
chr22:38646299
|
G | T | 1 | a0001c0001t0037g0130 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.143-654C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646299 | ||||||
chr22:38646320
|
C | T | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.143-675G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646320 | ||||||
chr22:38646328
|
C | T | 1 | a0001c0001t0003g0235 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.143-683G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646328 | ||||||
chr22:38646416
|
C | T | 8 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0151others(5): Show | 8 | HG02027.hp2 HG02056.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.143-771G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646416 | ||||||
chr22:38646423
|
C | T | 1 | a0001c0001t0002g0234 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.143-778G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646423 | ||||||
chr22:38646426
|
ATTT | A | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.143-784_143-782del others(3): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646426 | ||||||
chr22:38646541
|
C | T | 1 | a0002c0002t0015g0177 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.143-896G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646541 | ||||||
chr22:38646556
|
C | T | 1 | a0001c0001t0002g0315 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.143-911G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646556 | ||||||
chr22:38646657
|
A | T | 6 | a0001c0001t0002g0324a0001c0001t0016g0294a0001c0001t0016g0295others(3): Show | 6 | HG02055.hp2 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-1012T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646657 | ||||||
chr22:38646660
|
T | A | 2 | a0001c0001t0009g0217a0001c0001t0009g0218 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.143-1015A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646660 | ||||||
chr22:38646769
|
A | T | 1 | a0001c0001t0003g0232 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.143-1124T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646769 | ||||||
chr22:38646813
|
C | A | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.143-1168G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646813 | ||||||
chr22:38647016
|
G | A | 106 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(103): Show | 107 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.143-1371C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38647016 | ||||||
chr22:38647132
|
G | A | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.143-1487C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38647132 | ||||||
chr22:38647153
|
ATAAAT | A | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(3): Show | 6 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-1513_143-1509d others(7): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38647153 | ||||||
chr22:38647154
|
TAAATA | T | 109 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(106): Show | 110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.143-1514_143-1510d others(7): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38647154 | ||||||
chr22:38647169
|
A | C | 1 | a0001c0001t0003g0232 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.143-1524T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38647169 | ||||||
chr22:38647193
|
G | A | 1 | a0001c0001t0002g0308 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.143-1548C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38647193 | ||||||
chr22:38647471
|
C | CA | 8 | a0001c0001t0003g0293a0001c0001t0014g0163a0001c0001t0014g0164others(5): Show | 8 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-1827dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38647471 | ||||||
chr22:38647486
|
T | G | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.143-1841A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38647486 | ||||||
chr22:38648078
|
G | A | 23 | a0001c0001t0005g0005a0001c0001t0005g0014a0001c0001t0005g0016others(20): Show | 23 | HG00735.hp1 HG01261.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.142+1949C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648078 | ||||||
chr22:38648094
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.142+1933C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648094 | ||||||
chr22:38648146
|
T | C | 1 | a0001c0003t0013g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.142+1881A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648146 | ||||||
chr22:38648147
|
G | C | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.142+1880C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648147 | ||||||
chr22:38648305
|
T | TA | 44 | a0001c0001t0005g0031a0001c0001t0042g0145a0002c0002t0004g0171others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.142+1721dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648305 | ||||||
chr22:38648305
|
TA | T | 115 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(112): Show | 116 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.142+1721delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648305 | ||||||
chr22:38648357
|
AAGCACTT others(358): Show |
A | 7 | a0001c0001t0014g0163a0001c0001t0014g0164a0001c0001t0014g0165others(4): Show | 7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.142+1305_142+1669d others(2): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648357 | ||||||
chr22:38648422
|
A | C | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.142+1605T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648422 | ||||||
chr22:38648443
|
T | C | 4 | a0002c0002t0004g0203a0002c0002t0004g0204a0002c0002t0004g0213others(1): Show | 4 | HG04184.hp1 NA18974.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+1584A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648443 | ||||||
chr22:38648531
|
C | T | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.142+1496G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648531 | ||||||
chr22:38648555
|
C | T | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.142+1472G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648555 | ||||||
chr22:38648608
|
G | GAAAC | 109 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(106): Show | 110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.142+1415_142+1418d others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648608 | ||||||
chr22:38648649
|
G | A | 43 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(40): Show | 43 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.142+1378C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648649 | ||||||
chr22:38648700
|
C | T | 1 | a0001c0001t0005g0016 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.142+1327G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648700 | ||||||
chr22:38648801
|
C | T | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.142+1226G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648801 | ||||||
chr22:38648873
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.142+1154C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648873 | ||||||
chr22:38648971
|
C | CA | 6 | a0001c0001t0030g0038a0001c0001t0045g0127a0002c0002t0011g0205others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+1055dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648971 | ||||||
chr22:38648971
|
CA | C | 104 | a0001c0001t0001g0048a0001c0001t0002g0004a0001c0001t0002g0216others(101): Show | 105 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.142+1055delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648971 | ||||||
chr22:38649094
|
T | C | 157 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.142+933A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649094 | ||||||
chr22:38649335
|
C | G | 1 | a0001c0001t0003g0293 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.142+692G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649335 | ||||||
chr22:38649336
|
G | C | 1 | a0001c0001t0003g0293 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.142+691C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649336 | ||||||
chr22:38649427
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.142+600T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649427 | ||||||
chr22:38649456
|
C | T | 1 | a0001c0001t0003g0221 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.142+571G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649456 | ||||||
chr22:38649565
|
C | CA | 9 | a0001c0001t0001g0003a0001c0001t0016g0294a0001c0001t0016g0295others(6): Show | 10 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+461dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649565 | ||||||
chr22:38649787
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.142+240C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649787 | ||||||
chr22:38649879
|
AGAAAG | A | 106 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(103): Show | 107 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.142+143_142+147del others(5): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649879 | ||||||
chr22:38649879
|
AGAAAGAA others(3): Show |
A | 2 | a0001c0001t0009g0217a0001c0001t0009g0218 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.142+138_142+147del others(10): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649879 | ||||||
chr22:38649889
|
G | A | 1 | a0001c0001t0003g0232 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.142+138C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649889 | ||||||
chr22:38649890
|
A | G | 1 | a0001c0001t0003g0232 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.142+137T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649890 | ||||||
chr22:38650023
|
A | G | 1 | a0001c0001t0002g0299 | 1 | HG02280.hp2 | splice_region_variant&intron_variant | LOW | c.142+4T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38650023 | ||||||
chr22:38650322
|
T | C | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-94-60A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38650322 | ||||||
chr22:38650695
|
A | C | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-94-433T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38650695 | ||||||
chr22:38650715
|
C | T | 5 | a0001c0001t0003g0220a0001c0001t0003g0229a0001c0001t0003g0230others(2): Show | 5 | NA18980.hp2 NA18983.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.-94-453G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38650715 | ||||||
chr22:38650849
|
T | G | 1 | a0001c0001t0001g0128 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-94-587A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38650849 | ||||||
chr22:38651273
|
C | G | 1 | a0002c0004t0046g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-94-1011G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38651273 | ||||||
chr22:38651430
|
G | T | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-94-1168C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38651430 | ||||||
chr22:38651438
|
A | G | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-94-1176T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38651438 | ||||||
chr22:38651523
|
G | A | 1 | a0001c0001t0014g0166 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-94-1261C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38651523 | ||||||
chr22:38651795
|
G | GCT | 157 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.-94-1534_-94-1533i others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38651795 | ||||||
chr22:38651886
|
T | C | 1 | a0001c0001t0030g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-94-1624A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38651886 | ||||||
chr22:38651989
|
C | T | 47 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170others(44): Show | 47 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.-94-1727G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38651989 | ||||||
chr22:38652186
|
AAAAT | A | 47 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170others(44): Show | 47 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.-94-1928_-94-1925d others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652186 | ||||||
chr22:38652281
|
A | T | 1 | a0001c0001t0001g0046 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-94-2019T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652281 | ||||||
chr22:38652311
|
A | G | 157 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.-94-2049T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652311 | ||||||
chr22:38652444
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG01071.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-94-2182G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652444 | ||||||
chr22:38652609
|
G | A | 6 | a0001c0001t0007g0132a0001c0001t0008g0039a0001c0001t0008g0040others(3): Show | 6 | HG01175.hp2 HG01243.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-94-2347C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652609 | ||||||
chr22:38652713
|
C | T | 23 | a0001c0001t0005g0005a0001c0001t0005g0014a0001c0001t0005g0016others(20): Show | 23 | HG00735.hp1 HG01261.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.-94-2451G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652713 | ||||||
chr22:38652738
|
G | A | 2 | a0001c0001t0002g0004a0001c0001t0002g0297 | 3 | HG03490.hp2 HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-94-2476C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652738 | ||||||
chr22:38652750
|
T | G | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-94-2488A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652750 | ||||||
chr22:38652800
|
C | T | 1 | a0001c0001t0002g0324 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-94-2538G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652800 | ||||||
chr22:38652872
|
A | G | 207 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(204): Show | 208 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.-94-2610T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652872 | ||||||
chr22:38652876
|
C | CA | 17 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0001g0146others(14): Show | 17 | HG00140.hp1 HG00738.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.-94-2615dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652876 | ||||||
chr22:38652876
|
CA | C | 12 | a0001c0001t0001g0013a0001c0001t0002g0299a0001c0001t0002g0300others(9): Show | 12 | HG01175.hp1 HG02280.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-94-2615delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652876 | ||||||
chr22:38652876
|
CAA | C | 99 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(96): Show | 100 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.-94-2616_-94-2615d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652876 | ||||||
chr22:38652900
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-94-2638G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652900 | ||||||
chr22:38653037
|
T | C | 1 | a0001c0001t0023g0140 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-94-2775A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653037 | ||||||
chr22:38653051
|
T | C | 1 | a0001c0001t0031g0154 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-94-2789A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653051 | ||||||
chr22:38653225
|
A | C | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-95+2895T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653225 | ||||||
chr22:38653312
|
A | G | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-95+2808T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653312 | ||||||
chr22:38653337
|
T | C | 1 | a0001c0001t0005g0141 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-95+2783A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653337 | ||||||
chr22:38653377
|
C | CT | 97 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(94): Show | 98 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-95+2742dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653377 | ||||||
chr22:38653377
|
C | CTT | 10 | a0001c0001t0002g0223a0001c0001t0002g0224a0001c0001t0002g0225others(7): Show | 10 | HG00609.hp2 HG00741.hp2 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.-95+2741_-95+2742d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653377 | ||||||
chr22:38653587
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-95+2533C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653587 | ||||||
chr22:38653607
|
C | T | 2 | a0001c0001t0009g0217a0001c0001t0009g0218 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-95+2513G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653607 | ||||||
chr22:38653889
|
A | G | 1 | a0001c0001t0001g0013 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-95+2231T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653889 | ||||||
chr22:38654114
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-95+2006G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38654114 | ||||||
chr22:38654145
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-95+1975G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38654145 | ||||||
chr22:38654226
|
T | C | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.-95+1894A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38654226 | ||||||
chr22:38654241
|
T | G | 2 | a0001c0001t0009g0312a0001c0001t0009g0313 | 2 | HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-95+1879A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38654241 | ||||||
chr22:38654775
|
C | CA | 8 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0005g0142others(5): Show | 8 | HG00140.hp1 HG01928.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95+1344dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38654775 | ||||||
chr22:38654775
|
CA | C | 142 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(139): Show | 143 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.-95+1344delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38654775 | ||||||
chr22:38655009
|
G | A | 3 | a0001c0001t0018g0168a0001c0001t0018g0169a0001c0001t0018g0170 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-95+1111C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655009 | ||||||
chr22:38655119
|
G | A | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-95+1001C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655119 | ||||||
chr22:38655306
|
G | C | 44 | a0002c0002t0004g0171a0002c0002t0004g0172a0002c0002t0004g0178others(41): Show | 44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.-95+814C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655306 | ||||||
chr22:38655339
|
G | A | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-95+781C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655339 | ||||||
chr22:38655356
|
G | A | 8 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0151others(5): Show | 8 | HG02027.hp2 HG02056.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.-95+764C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655356 | ||||||
chr22:38655392
|
A | G | 2 | a0001c0001t0009g0217a0001c0001t0009g0218 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-95+728T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655392 | ||||||
chr22:38655423
|
T | C | 170 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(167): Show | 171 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.-95+697A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655423 | ||||||
chr22:38655671
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-95+449A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655671 | ||||||
chr22:38655700
|
C | T | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-95+420G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655700 | ||||||
chr22:38655785
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-95+335G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655785 | ||||||
chr22:38656006
|
C | A | 1 | a0001c0001t0002g0324 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-95+114G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38656006 | ||||||
chr22:38656037
|
T | A | 1 | a0001c0001t0001g0006 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-95+83A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38656037 | ||||||
chr22:38656045
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-95+75C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38656045 | ||||||
chr22:38656081
|
C | T | 1 | a0001c0001t0005g0005 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-95+39G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38656081 | ||||||
chr22:38656111
|
C | T | 110 | a0001c0001t0002g0004a0001c0001t0002g0216a0001c0001t0002g0219others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-95+9G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38656111 |