geneid | 3895 |
---|---|
ensemblid | ENSG00000126777.18 |
hgncid | 6467 |
symbol | KTN1 |
name | kinectin 1 |
refseq_nuc | NM_001079521.2 |
refseq_prot | NP_001072989.1 |
ensembl_nuc | ENST00000395314.8 |
ensembl_prot | ENSP00000378725.3 |
mane_status | MANE Select |
chr | chr14 |
start | 55580207 |
end | 55684579 |
strand | + |
ver | v1.2 |
region | chr14:55580207-55684579 |
region5000 | chr14:55575207-55689579 |
regionname0 | KTN1_chr14_55580207_55684579 |
regionname5000 | KTN1_chr14_55575207_55689579 |
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 | 1357 | 294 | 56 | 62 | 135 | 10 | 29 | 109 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0002 | 0/0 | 1357 | 5 | 3 | 0 | 0 | 0 | 2 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0003 | 0/0 | 1357 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0004 | 0/0 | 1357 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0005 | 0/0 | 1357 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0006 | 0/0 | 1357 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0007 | 0/0 | 1357 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0008 | 0/0 | 1357 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0009 | 0/0 | 1357 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0010 | 0/0 | 1357 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0011 | 0/0 | 1357 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0012 | 0/0 | 1357 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0013 | 0/0 | 1357 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
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 | 4074 | 273 | 49 | 53 | 132 | 9 | 28 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0002 | 0/0 | 4074 | 13 | 2 | 8 | 1 | 1 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0003 | 0/0 | 4074 | 5 | 3 | 0 | 0 | 0 | 2 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0004 | 0/0 | 4074 | 3 | 3 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0005 | 0/0 | 4074 | 2 | 0 | 0 | 2 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0006 | 0/0 | 4074 | 2 | 0 | 0 | 2 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0007 | 0/0 | 4074 | 2 | 0 | 0 | 0 | 0 | 2 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0008 | 0/0 | 4074 | 2 | 2 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0009 | 0/0 | 4074 | 2 | 2 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0010 | 0/0 | 4074 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0011 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0012 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0013 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0014 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0015 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0016 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0017 | 0/0 | 4074 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0018 | 0/0 | 4074 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
c0019 | 0/0 | 4074 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
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 | 1/1 | 655 | 190 | 47 | 42 | 78 | 4 | 17 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
t0002 | 0/0 | 649 | 82 | 5 | 11 | 48 | 4 | 14 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
t0003 | 0/0 | 649 | 29 | 12 | 9 | 4 | 1 | 3 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
t0004 | 0/0 | 658 | 5 | 0 | 0 | 5 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
t0005 | 0/0 | 655 | 4 | 1 | 0 | 3 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
t0006 | 0/0 | 640 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
t0007 | 0/0 | 655 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
t0008 | 0/0 | 655 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
t0009 | 0/0 | 667 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
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 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0196 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
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 | 4074 | 273 | 49 | 53 | 132 | 9 | 28 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0002 | 0/0 | 4074 | 13 | 2 | 8 | 1 | 1 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0004 | 0/0 | 4074 | 3 | 3 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0005 | 0/0 | 4074 | 2 | 0 | 0 | 2 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0009 | 0/0 | 4074 | 2 | 2 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0018 | 0/0 | 4074 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0002c0003 | 0/0 | 4074 | 5 | 3 | 0 | 0 | 0 | 2 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0003c0016 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0003c0019 | 0/0 | 4074 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0004c0007 | 0/0 | 4074 | 2 | 0 | 0 | 0 | 0 | 2 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0005c0006 | 0/0 | 4074 | 2 | 0 | 0 | 2 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0006c0008 | 0/0 | 4074 | 2 | 2 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0007c0017 | 0/0 | 4074 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0008c0012 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0009c0014 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0010c0011 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0011c0015 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0012c0013 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0013c0010 | 0/0 | 4074 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4728 | 181 | 42 | 40 | 76 | 4 | 17 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0001t0002 | 0/0 | 4722 | 76 | 5 | 11 | 45 | 4 | 11 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0001t0003 | 0/0 | 4722 | 4 | 1 | 0 | 3 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0001t0004 | 0/0 | 4731 | 5 | 0 | 0 | 5 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0001t0005 | 0/0 | 4728 | 3 | 0 | 0 | 3 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0001t0006 | 0/0 | 4713 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0001t0007 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0001t0008 | 0/0 | 4728 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0001t0009 | 0/0 | 4740 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0002t0003 | 0/0 | 4722 | 13 | 2 | 8 | 1 | 1 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0004t0003 | 0/0 | 4722 | 3 | 3 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0005t0001 | 0/0 | 4728 | 2 | 0 | 0 | 2 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0009t0001 | 0/0 | 4728 | 2 | 2 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0001c0018t0001 | 0/0 | 4728 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0002c0003t0003 | 0/0 | 4722 | 5 | 3 | 0 | 0 | 0 | 2 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0003c0016t0003 | 0/0 | 4722 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0003c0019t0003 | 0/0 | 4722 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0004c0007t0002 | 0/0 | 4722 | 2 | 0 | 0 | 0 | 0 | 2 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0005c0006t0002 | 0/0 | 4722 | 2 | 0 | 0 | 2 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0006c0008t0003 | 0/0 | 4722 | 2 | 2 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0007c0017t0002 | 0/0 | 4722 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0008c0012t0002 | 0/0 | 4722 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0009c0014t0001 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0010c0011t0005 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0011c0015t0001 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0012c0013t0001 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
a0013c0010t0001 | 0/0 | 4728 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | copy fasta | chr14 | 55575207 | 55689579 |
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 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0196 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0006g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0008g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0001t0009g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0002t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0002t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0002t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0002t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0002t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0002t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0002t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0002t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0002t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0002t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0004t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0004t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0004t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0005t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0005t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0009t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0009t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0001c0018t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0002c0003t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0002c0003t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0002c0003t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0002c0003t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0002c0003t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0003c0016t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0003c0019t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0004c0007t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0004c0007t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0005c0006t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0005c0006t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0006c0008t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0006c0008t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0007c0017t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0008c0012t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0009c0014t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0010c0011t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0011c0015t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0012c0013t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
a0013c0010t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00099 | hp2 | a0001 | c0002 | t0003 | g0185 | EUR | GBR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | FIN | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00323 | hp2 | a0001 | c0001 | t0009 | g0260 | EUR | FIN | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00639 | hp2 | a0003 | c0019 | t0003 | g0189 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00738 | hp1 | a0001 | c0001 | t0008 | g0141 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01074 | hp2 | a0001 | c0002 | t0003 | g0179 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01081 | hp1 | a0001 | c0002 | t0003 | g0180 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01169 | hp2 | a0001 | c0002 | t0003 | g0181 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01175 | hp2 | a0001 | c0002 | t0003 | g0176 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01256 | hp1 | a0001 | c0002 | t0003 | g0182 | AMR | CLM | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0278 | EUR | IBS | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0078 | EUR | IBS | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0293 | EUR | IBS | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | IBS | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01884 | hp1 | a0002 | c0003 | t0003 | g0191 | AFR | ACB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01928 | hp1 | a0013 | c0010 | t0001 | g0144 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01934 | hp2 | a0001 | c0002 | t0003 | g0177 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01943 | hp2 | a0001 | c0002 | t0003 | g0183 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01981 | hp1 | a0001 | c0018 | t0001 | g0310 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02055 | hp2 | a0001 | c0001 | t0007 | g0174 | AFR | ACB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | ACB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | CDX | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | CDX | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02257 | hp1 | a0002 | c0003 | t0003 | g0192 | AFR | ACB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02258 | hp1 | a0001 | c0002 | t0003 | g0300 | AFR | ACB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02293 | hp2 | a0001 | c0001 | t0006 | g0297 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02300 | hp1 | a0001 | c0002 | t0003 | g0178 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02451 | hp1 | a0001 | c0002 | t0003 | g0175 | AFR | ACB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02698 | hp1 | a0004 | c0007 | t0002 | g0013 | SAS | PJL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02723 | hp1 | a0001 | c0004 | t0003 | g0005 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02738 | hp2 | a0007 | c0017 | t0002 | g0030 | SAS | PJL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03139 | hp1 | a0012 | c0013 | t0001 | g0111 | AFR | ESN | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03195 | hp2 | a0006 | c0008 | t0003 | g0188 | AFR | ESN | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03225 | hp1 | a0010 | c0011 | t0005 | g0173 | AFR | MSL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03486 | hp1 | a0006 | c0008 | t0003 | g0187 | AFR | MSL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03516 | hp1 | a0001 | c0004 | t0003 | g0006 | AFR | ESN | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03540 | hp2 | a0011 | c0015 | t0001 | g0085 | AFR | GWD | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0286 | SAS | PJL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | STU | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | STU | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03831 | hp2 | a0004 | c0007 | t0002 | g0287 | SAS | BEB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | BEB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03927 | hp1 | a0001 | c0002 | t0003 | g0184 | SAS | BEB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | BEB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | BEB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0288 | SAS | BEB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG04184 | hp2 | a0002 | c0003 | t0003 | g0301 | SAS | BEB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0290 | SAS | STU | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG04199 | hp2 | a0002 | c0003 | t0003 | g0193 | SAS | STU | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | STU | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | STU | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18522 | hp2 | a0002 | c0003 | t0003 | g0194 | AFR | YRI | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | CHB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18906 | hp2 | a0001 | c0009 | t0001 | g0084 | AFR | YRI | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18957 | hp1 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18966 | hp2 | a0008 | c0012 | t0002 | g0060 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18968 | hp2 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18975 | hp1 | a0005 | c0006 | t0002 | g0040 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18988 | hp1 | a0005 | c0006 | t0002 | g0051 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18993 | hp2 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18994 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19012 | hp1 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19043 | hp1 | a0001 | c0004 | t0003 | g0003 | AFR | LWK | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | LWK | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19075 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19084 | hp1 | a0001 | c0005 | t0001 | g0277 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA19090 | hp2 | a0001 | c0005 | t0001 | g0272 | EAS | JPT | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ASW | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ASW | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | TSI | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0071 | EUR | TSI | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | GIH | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | GIH | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02559 | hp1 | a0003 | c0016 | t0003 | g0190 | AFR | ACB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG06807 | hp1 | a0009 | c0014 | t0001 | g0172 | AFR | USA | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | USA | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | USA | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | USA | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA21309 | hp1 | a0001 | c0009 | t0001 | g0086 | AFR | LWK | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | LWK | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0196 | REF | REF | KTN1_chr14_55575207_55689579 | KTN1 | chr14 | 55575207 | 55689579 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:55612021
|
T | G | 6 | a0001a0004a0005others(3): Show | 88 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(85): Show |
splice_region_variant | LOW | c.-28T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/44 | chr14 | 55612021 | ||||||
chr14:55612340
|
G | A | 1 | a0013 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.292G>A | p.Ala98Thr | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/44 | 470/4728 | 292/4074 | 98/1357 | chr14 | 55612340 | ||
chr14:55618094
|
G | T | 1 | a0007 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.792G>T | p.Gln264His | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 4/44 | 970/4728 | 792/4074 | 264/1357 | chr14 | 55618094 | ||
chr14:55627933
|
A | G | 1 | a0003 | 2 | HG00639.hp2 HG02559.hp1 |
missense_variant | MODERATE | c.985A>G | p.Thr329Ala | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/44 | 1163/4728 | 985/4074 | 329/1357 | chr14 | 55627933 | ||
chr14:55636513
|
C | T | 1 | a0012 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.1526C>T | p.Ala509Val | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 10/44 | 1704/4728 | 1526/4074 | 509/1357 | chr14 | 55636513 | ||
chr14:55639918
|
C | G | 1 | a0011 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1829C>G | p.Ala610Gly | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 14/44 | 2007/4728 | 1829/4074 | 610/1357 | chr14 | 55639918 | ||
chr14:55639948
|
A | C | 1 | a0004 | 2 | HG02698.hp1 HG03831.hp2 |
missense_variant | MODERATE | c.1859A>C | p.Glu620Ala | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 14/44 | 2037/4728 | 1859/4074 | 620/1357 | chr14 | 55639948 | ||
chr14:55639971
|
G | A | 1 | a0006 | 2 | HG03195.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.1882G>A | p.Asp628Asn | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 14/44 | 2060/4728 | 1882/4074 | 628/1357 | chr14 | 55639971 | ||
chr14:55639980
|
A | G | 1 | a0005 | 2 | NA18975.hp1 NA18988.hp1 |
missense_variant | MODERATE | c.1891A>G | p.Thr631Ala | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 14/44 | 2069/4728 | 1891/4074 | 631/1357 | chr14 | 55639980 | ||
chr14:55640948
|
G | C | 1 | a0002 | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
missense_variant | MODERATE | c.1999G>C | p.Glu667Gln | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 16/44 | 2177/4728 | 1999/4074 | 667/1357 | chr14 | 55640948 | ||
chr14:55648105
|
A | C | 1 | a0008 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.2288A>C | p.Glu763Ala | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 20/44 | 2466/4728 | 2288/4074 | 763/1357 | chr14 | 55648105 | ||
chr14:55651921
|
A | G | 1 | a0010 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.2597A>G | p.Gln866Arg | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/44 | 2775/4728 | 2597/4074 | 866/1357 | chr14 | 55651921 | ||
chr14:55678416
|
T | C | 1 | a0009 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.3920T>C | p.Ile1307Thr | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 42/44 | 4098/4728 | 3920/4074 | 1307/1357 | chr14 | 55678416 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:55612270
|
A | G | 1 | a0003c0019 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.222A>G | p.Glu74Glu | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/44 | 400/4728 | 222/4074 | 74/1357 | chr14 | 55612270 | ||
chr14:55612321
|
A | T | 1 | a0001c0018 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.273A>T | p.Ala91Ala | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/44 | 451/4728 | 273/4074 | 91/1357 | chr14 | 55612321 | ||
chr14:55628008
|
C | A | 1 | a0001c0004 | 3 | HG02723.hp1 HG03516.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.1060C>A | p.Arg354Arg | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/44 | 1238/4728 | 1060/4074 | 354/1357 | chr14 | 55628008 | ||
chr14:55629968
|
A | C | 3 | a0001c0009a0009c0014a0011c0015 | 4 | HG03540.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
synonymous_variant | LOW | c.1092A>C | p.Thr364Thr | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/44 | 1270/4728 | 1092/4074 | 364/1357 | chr14 | 55629968 | ||
chr14:55630013
|
A | G | 5 | a0001c0002a0002c0003a0003c0016others(2): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
synonymous_variant | LOW | c.1137A>G | p.Arg379Arg | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/44 | 1315/4728 | 1137/4074 | 379/1357 | chr14 | 55630013 | ||
chr14:55639190
|
C | T | 1 | a0002c0003 | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
synonymous_variant | LOW | c.1791C>T | p.Ser597Ser | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 13/44 | 1969/4728 | 1791/4074 | 597/1357 | chr14 | 55639190 | ||
chr14:55648076
|
T | C | 1 | a0001c0005 | 2 | NA19084.hp1 NA19090.hp2 |
synonymous_variant | LOW | c.2259T>C | p.Thr753Thr | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 20/44 | 2437/4728 | 2259/4074 | 753/1357 | chr14 | 55648076 | ||
chr14:55671640
|
C | T | 1 | a0001c0018 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.3423C>T | p.Ser1141Ser | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 36/44 | 3601/4728 | 3423/4074 | 1141/1357 | chr14 | 55671640 | ||
chr14:55679639
|
G | A | 5 | a0001c0002a0002c0003a0003c0016others(2): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
synonymous_variant | LOW | c.4023G>A | p.Ala1341Ala | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/44 | 4201/4728 | 4023/4074 | 1341/1357 | chr14 | 55679639 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:55580253
|
T | TGCG | 1 | a0001c0001t0004 | 5 | NA18981.hp1 NA18986.hp1 NA18994.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-107_-105dupGCG | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/44 | 31768 | INFO_REALIGN_3_PRIME | chr14 | 55580253 | ||||
chr14:55580253
|
T | TGCGGCGG others(5): Show |
1 | a0001c0001t0009 | 1 | HG00323.hp2 | 5_prime_UTR_variant | MODIFIER | c.-116_-105dupGCGGCG others(6): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/44 | 31768 | INFO_REALIGN_3_PRIME | chr14 | 55580253 | ||||
chr14:55580253
|
TGCGGCG | T | 12 | a0001c0001t0002a0001c0001t0003a0001c0002t0003others(9): Show | 111 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(108): Show |
5_prime_UTR_variant | MODIFIER | c.-110_-105delGCGGCG | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/44 | 31769 | INFO_REALIGN_3_PRIME | chr14 | 55580253 | ||||
chr14:55580253
|
TGCGGCGG others(8): Show |
T | 1 | a0001c0001t0006 | 1 | HG02293.hp2 | 5_prime_UTR_variant | MODIFIER | c.-119_-105delGCGGCG others(9): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/44 | 31769 | INFO_REALIGN_3_PRIME | chr14 | 55580253 | ||||
chr14:55684375
|
T | G | 1 | a0001c0001t0008 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*272T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 44/44 | 272 | chr14 | 55684375 | |||||
chr14:55684402
|
T | C | 1 | a0001c0001t0007 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*299T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 44/44 | 299 | chr14 | 55684402 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:55580460
|
C | CG | 28 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0298others(25): Show | 28 | HG00597.hp1 HG00597.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-31+113dupG | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55580460 | |||||
chr14:55580514
|
T | A | 1 | a0001c0004t0003g0003 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-31+160T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55580514 | ||||||
chr14:55580539
|
T | C | 209 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0088others(206): Show | 209 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.-31+185T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55580539 | ||||||
chr14:55580590
|
G | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+236G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55580590 | ||||||
chr14:55580592
|
G | T | 1 | a0001c0001t0001g0312 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-31+238G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55580592 | ||||||
chr14:55580611
|
C | A | 1 | a0001c0001t0001g0004 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-31+257C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55580611 | ||||||
chr14:55580634
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-31+280G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55580634 | ||||||
chr14:55580768
|
A | C | 1 | a0001c0001t0001g0311 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-31+414A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55580768 | ||||||
chr14:55580771
|
A | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0279a0001c0001t0001g0281others(4): Show | 8 | HG00544.hp2 HG01257.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.-31+417A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55580771 | ||||||
chr14:55580825
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-31+471C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55580825 | ||||||
chr14:55580845
|
C | G | 2 | a0001c0001t0007g0174a0010c0011t0005g0173 | 2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-31+491C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55580845 | ||||||
chr14:55580870
|
C | T | 9 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31+516C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55580870 | ||||||
chr14:55580950
|
C | T | 6 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 6 | NA18941.hp1 NA18950.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+596C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55580950 | ||||||
chr14:55581063
|
C | T | 27 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.-31+709C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55581063 | ||||||
chr14:55581076
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-31+722C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55581076 | ||||||
chr14:55581107
|
C | G | 9 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31+753C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55581107 | ||||||
chr14:55581108
|
C | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+754C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55581108 | ||||||
chr14:55581122
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-31+768C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55581122 | ||||||
chr14:55581133
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+779G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55581133 | ||||||
chr14:55581230
|
T | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+876T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55581230 | ||||||
chr14:55581442
|
G | GGT | 6 | a0001c0001t0001g0299a0002c0003t0003g0191a0002c0003t0003g0192others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+1104_-31+1105d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55581442 | |||||
chr14:55581473
|
G | T | 1 | a0009c0014t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-31+1119G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55581473 | ||||||
chr14:55581726
|
C | T | 8 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(5): Show | 8 | HG02109.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-31+1372C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55581726 | ||||||
chr14:55581745
|
TGCTGGTG others(22): Show |
T | 4 | a0001c0001t0003g0007a0001c0004t0003g0003a0001c0004t0003g0005others(1): Show | 4 | HG02723.hp1 HG03516.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+1422_-31+1450d others(31): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55581745 | |||||
chr14:55581917
|
T | TG | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+1563_-31+1564i others(3): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55581917 | ||||||
chr14:55582008
|
T | G | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | NA18974.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-31+1654T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55582008 | ||||||
chr14:55582133
|
C | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+1779C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55582133 | ||||||
chr14:55582188
|
G | A | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+1834G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55582188 | ||||||
chr14:55582355
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-31+2001C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55582355 | ||||||
chr14:55582411
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+2057G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55582411 | ||||||
chr14:55582435
|
C | G | 2 | a0003c0016t0003g0190a0003c0019t0003g0189 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-31+2081C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55582435 | ||||||
chr14:55582478
|
A | C | 4 | a0003c0016t0003g0190a0003c0019t0003g0189a0006c0008t0003g0187others(1): Show | 4 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+2124A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55582478 | ||||||
chr14:55582486
|
G | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0087others(219): Show | 224 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.-31+2132G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55582486 | ||||||
chr14:55582623
|
T | A | 1 | a0001c0004t0003g0003 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-31+2269T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55582623 | ||||||
chr14:55582821
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-31+2467A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55582821 | ||||||
chr14:55583028
|
G | A | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-31+2674G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55583028 | ||||||
chr14:55583082
|
T | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+2728T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55583082 | ||||||
chr14:55583197
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-31+2843T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55583197 | ||||||
chr14:55583284
|
T | TA | 9 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31+2936dupA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55583284 | |||||
chr14:55583312
|
T | G | 1 | a0001c0004t0003g0003 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-31+2958T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55583312 | ||||||
chr14:55583402
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-31+3048A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55583402 | ||||||
chr14:55583403
|
TGTAGAAG others(6): Show |
T | 1 | a0001c0001t0001g0162 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-31+3050_-31+3062d others(15): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55583403 | ||||||
chr14:55583487
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+3133G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55583487 | ||||||
chr14:55583628
|
C | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+3274C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55583628 | ||||||
chr14:55583734
|
A | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+3380A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55583734 | ||||||
chr14:55583748
|
C | G | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+3394C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55583748 | ||||||
chr14:55583760
|
G | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+3406G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55583760 | ||||||
chr14:55583813
|
G | T | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31+3459G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55583813 | ||||||
chr14:55584092
|
G | C | 1 | a0001c0001t0001g0004 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-31+3738G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584092 | ||||||
chr14:55584178
|
G | A | 119 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(116): Show | 119 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-31+3824G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584178 | ||||||
chr14:55584224
|
G | A | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31+3870G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584224 | ||||||
chr14:55584231
|
T | TA | 17 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(14): Show | 17 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.-31+3878dupA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55584231 | |||||
chr14:55584271
|
T | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+3917T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584271 | ||||||
chr14:55584281
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-31+3927G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584281 | ||||||
chr14:55584298
|
C | T | 3 | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0002g0294 | 3 | NA18946.hp2 NA18991.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-31+3944C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584298 | ||||||
chr14:55584327
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-31+3973T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584327 | ||||||
chr14:55584358
|
T | C | 1 | a0003c0019t0003g0189 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-31+4004T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584358 | ||||||
chr14:55584360
|
G | T | 1 | a0001c0001t0001g0298 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-31+4006G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584360 | ||||||
chr14:55584405
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-31+4051T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584405 | ||||||
chr14:55584420
|
A | G | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31+4066A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584420 | ||||||
chr14:55584522
|
A | G | 1 | a0001c0018t0001g0310 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-31+4168A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584522 | ||||||
chr14:55584555
|
T | C | 1 | a0001c0001t0002g0008 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-31+4201T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584555 | ||||||
chr14:55584609
|
T | C | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31+4255T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584609 | ||||||
chr14:55584632
|
T | G | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31+4278T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584632 | ||||||
chr14:55584640
|
C | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | NA18957.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-31+4286C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584640 | ||||||
chr14:55584647
|
G | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+4293G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584647 | ||||||
chr14:55584649
|
A | G | 72 | a0001c0001t0002g0008a0001c0001t0002g0020a0001c0001t0002g0021others(69): Show | 72 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.-31+4295A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584649 | ||||||
chr14:55584717
|
A | AAC | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+4367_-31+4368d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55584717 | |||||
chr14:55584722
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-31+4368A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584722 | ||||||
chr14:55584827
|
T | C | 11 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(8): Show | 11 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.-31+4473T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55584827 | ||||||
chr14:55585007
|
C | T | 6 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(3): Show | 6 | HG01168.hp2 HG01433.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31+4653C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55585007 | ||||||
chr14:55585131
|
C | CA | 39 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0088others(36): Show | 39 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.-31+4802dupA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55585131 | |||||
chr14:55585131
|
CA | C | 20 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0241others(17): Show | 20 | HG01074.hp2 HG01081.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.-31+4802delA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55585131 | |||||
chr14:55585131
|
CAA | C | 9 | a0001c0002t0003g0175a0001c0002t0003g0185a0002c0003t0003g0191others(6): Show | 9 | HG00099.hp2 HG00639.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31+4801_-31+4802d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55585131 | |||||
chr14:55585161
|
A | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+4807A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55585161 | ||||||
chr14:55585326
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-31+4972T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55585326 | ||||||
chr14:55585509
|
T | G | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31+5155T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55585509 | ||||||
chr14:55585630
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | NA18957.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-31+5276A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55585630 | ||||||
chr14:55585661
|
T | C | 1 | a0001c0001t0002g0032 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-31+5307T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55585661 | ||||||
chr14:55585826
|
G | A | 4 | a0001c0001t0003g0007a0001c0004t0003g0003a0001c0004t0003g0005others(1): Show | 4 | HG02723.hp1 HG03516.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+5472G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55585826 | ||||||
chr14:55585856
|
C | T | 4 | a0001c0001t0001g0251a0001c0001t0001g0269a0001c0001t0001g0270others(1): Show | 4 | HG00639.hp1 HG01517.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+5502C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55585856 | ||||||
chr14:55586284
|
G | A | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+5930G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55586284 | ||||||
chr14:55586418
|
T | TTATCA | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31+6078_-31+6082d others(7): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55586418 | |||||
chr14:55586420
|
A | ATCATG | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+6070_-31+6071i others(7): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55586420 | |||||
chr14:55586529
|
G | T | 86 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(83): Show | 86 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.-31+6175G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55586529 | ||||||
chr14:55586643
|
T | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+6289T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55586643 | ||||||
chr14:55586942
|
C | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+6588C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55586942 | ||||||
chr14:55587104
|
C | CTG | 96 | a0001c0001t0001g0004a0001c0001t0001g0155a0001c0001t0001g0156others(93): Show | 96 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-31+6752_-31+6753d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55587104 | |||||
chr14:55587145
|
C | G | 23 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(20): Show | 23 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.-31+6791C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55587145 | ||||||
chr14:55587147
|
A | G | 11 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(8): Show | 11 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-31+6793A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55587147 | ||||||
chr14:55587278
|
A | G | 11 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(8): Show | 11 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-31+6924A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55587278 | ||||||
chr14:55587583
|
C | T | 23 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(20): Show | 23 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.-31+7229C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55587583 | ||||||
chr14:55587593
|
C | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+7239C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55587593 | ||||||
chr14:55587636
|
T | C | 23 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(20): Show | 23 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.-31+7282T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55587636 | ||||||
chr14:55587708
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-31+7354A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55587708 | ||||||
chr14:55587752
|
T | C | 4 | a0001c0001t0003g0007a0001c0004t0003g0003a0001c0004t0003g0005others(1): Show | 4 | HG02723.hp1 HG03516.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+7398T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55587752 | ||||||
chr14:55587924
|
T | C | 23 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(20): Show | 23 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.-31+7570T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55587924 | ||||||
chr14:55587924
|
TTAGTCTA others(5): Show |
T | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-31+7572_-31+7583d others(14): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55587924 | |||||
chr14:55587926
|
A | G | 23 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(20): Show | 23 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.-31+7572A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55587926 | ||||||
chr14:55587952
|
A | G | 11 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(8): Show | 11 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-31+7598A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55587952 | ||||||
chr14:55588013
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-31+7659C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55588013 | ||||||
chr14:55588172
|
A | G | 1 | a0001c0001t0001g0308 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-31+7818A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55588172 | ||||||
chr14:55588357
|
A | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | NA18946.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-31+8003A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55588357 | ||||||
chr14:55588685
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG02080.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-31+8331C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55588685 | ||||||
chr14:55588728
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0195others(97): Show | 102 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.-31+8374C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55588728 | ||||||
chr14:55588744
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-31+8390C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55588744 | ||||||
chr14:55588824
|
G | A | 1 | a0001c0001t0002g0033 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-31+8470G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55588824 | ||||||
chr14:55588908
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-31+8554G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55588908 | ||||||
chr14:55588985
|
AT | A | 5 | a0001c0001t0001g0087a0001c0001t0001g0095a0001c0001t0001g0096others(2): Show | 5 | HG02970.hp2 HG03195.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+8632delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55588985 | ||||||
chr14:55589214
|
T | C | 1 | a0010c0011t0005g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-31+8860T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55589214 | ||||||
chr14:55589235
|
T | C | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31+8881T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55589235 | ||||||
chr14:55589426
|
C | A | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+9072C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55589426 | ||||||
chr14:55589471
|
C | T | 2 | a0001c0001t0002g0083a0001c0001t0002g0294 | 2 | NA18991.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-31+9117C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55589471 | ||||||
chr14:55589656
|
C | CT | 66 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0091others(63): Show | 66 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.-31+9322dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55589656 | |||||
chr14:55589656
|
C | CTT | 6 | a0001c0001t0001g0271a0001c0001t0002g0010a0001c0001t0002g0023others(3): Show | 6 | HG00323.hp1 HG02055.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+9321_-31+9322d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55589656 | |||||
chr14:55589656
|
C | CTTT | 79 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0011others(76): Show | 79 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-31+9320_-31+9322d others(5): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55589656 | |||||
chr14:55589656
|
CT | C | 24 | a0001c0001t0001g0099a0001c0001t0001g0246a0001c0001t0001g0253others(21): Show | 24 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.-31+9322delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55589656 | |||||
chr14:55589744
|
C | T | 1 | a0010c0011t0005g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-31+9390C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55589744 | ||||||
chr14:55589844
|
A | G | 61 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(58): Show | 61 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.-31+9490A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55589844 | ||||||
chr14:55589995
|
A | AAAAAC | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+9656_-31+9660d others(7): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55589995 | |||||
chr14:55590112
|
T | C | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31+9758T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55590112 | ||||||
chr14:55590157
|
A | T | 1 | a0001c0001t0002g0290 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-31+9803A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55590157 | ||||||
chr14:55590332
|
A | T | 7 | a0001c0001t0002g0023a0001c0001t0002g0031a0001c0001t0002g0071others(4): Show | 7 | HG00323.hp1 HG00738.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+9978A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55590332 | ||||||
chr14:55590398
|
ACGTATGA others(10): Show |
A | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-31+10045_-31+1006 others(21): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55590398 | ||||||
chr14:55590419
|
G | A | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-31+10065G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55590419 | ||||||
chr14:55590506
|
C | G | 4 | a0001c0001t0003g0007a0001c0004t0003g0003a0001c0004t0003g0005others(1): Show | 4 | HG02723.hp1 HG03516.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+10152C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55590506 | ||||||
chr14:55590679
|
C | CT | 8 | a0001c0001t0001g0154a0001c0001t0001g0268a0001c0001t0003g0022others(5): Show | 8 | HG00639.hp2 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-31+10339dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55590679 | |||||
chr14:55590706
|
C | T | 1 | a0001c0001t0002g0077 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-31+10352C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55590706 | ||||||
chr14:55590864
|
C | T | 121 | a0001c0001t0001g0004a0001c0001t0001g0296a0001c0001t0001g0299others(118): Show | 121 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.-31+10510C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55590864 | ||||||
chr14:55591062
|
A | AT | 26 | a0001c0001t0003g0007a0001c0002t0003g0175a0001c0002t0003g0176others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.-31+10710dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55591062 | |||||
chr14:55591162
|
G | GT | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+10816dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55591162 | |||||
chr14:55591190
|
C | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0195others(97): Show | 102 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.-31+10836C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55591190 | ||||||
chr14:55591331
|
A | G | 6 | a0001c0001t0001g0087a0001c0001t0001g0095a0001c0001t0001g0096others(3): Show | 6 | HG02970.hp2 HG03195.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+10977A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55591331 | ||||||
chr14:55591432
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-31+11078A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55591432 | ||||||
chr14:55591529
|
T | G | 9 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31+11175T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55591529 | ||||||
chr14:55591577
|
CTTTCTTT others(6): Show |
C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+11227_-31+1123 others(17): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55591577 | |||||
chr14:55591581
|
C | CT | 14 | a0001c0001t0001g0004a0001c0001t0001g0093a0001c0001t0001g0094others(11): Show | 14 | HG00423.hp2 HG01071.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.-31+11251dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55591581 | |||||
chr14:55591581
|
CT | C | 83 | a0001c0001t0001g0100a0001c0001t0001g0114a0001c0001t0001g0118others(80): Show | 83 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.-31+11251delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55591581 | |||||
chr14:55591581
|
CTTTTTTT | C | 7 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(4): Show | 7 | NA18949.hp2 NA18952.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+11245_-31+1125 others(11): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55591581 | |||||
chr14:55591581
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0279 | 3 | HG01943.hp1 NA18971.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-31+11242_-31+1125 others(14): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55591581 | |||||
chr14:55591581
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0205 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-31+11241_-31+1125 others(15): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55591581 | |||||
chr14:55591581
|
CTTTTTTT others(7): Show |
C | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31+11238_-31+1125 others(18): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55591581 | |||||
chr14:55591589
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0312 | 2 | HG01934.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-31+11235T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55591589 | ||||||
chr14:55591593
|
T | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+11239T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55591593 | ||||||
chr14:55591595
|
T | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+11241T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55591595 | ||||||
chr14:55591602
|
T | C | 1 | a0001c0001t0002g0033 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-31+11248T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55591602 | ||||||
chr14:55591629
|
C | T | 9 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0142others(6): Show | 9 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31+11275C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55591629 | ||||||
chr14:55591976
|
T | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+11622T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55591976 | ||||||
chr14:55592044
|
T | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+11690T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55592044 | ||||||
chr14:55592072
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-31+11718C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55592072 | ||||||
chr14:55592187
|
C | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+11833C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55592187 | ||||||
chr14:55592208
|
A | G | 1 | a0009c0014t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-31+11854A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55592208 | ||||||
chr14:55592464
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-31+12110G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55592464 | ||||||
chr14:55592476
|
C | T | 1 | a0009c0014t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-31+12122C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55592476 | ||||||
chr14:55592863
|
A | G | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | NA18974.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-31+12509A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55592863 | ||||||
chr14:55592960
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-31+12606C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55592960 | ||||||
chr14:55593061
|
C | T | 5 | a0001c0001t0001g0087a0001c0001t0001g0095a0001c0001t0001g0096others(2): Show | 5 | HG02970.hp2 HG03195.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+12707C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55593061 | ||||||
chr14:55593088
|
A | T | 97 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0142others(94): Show | 97 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.-31+12734A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55593088 | ||||||
chr14:55593162
|
TG | T | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31+12809delG | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55593162 | ||||||
chr14:55593269
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+12915G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55593269 | ||||||
chr14:55593436
|
A | AC | 95 | a0001c0001t0001g0100a0001c0001t0001g0112a0001c0001t0001g0120others(92): Show | 95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.-31+13092dupC | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55593436 | |||||
chr14:55593436
|
A | ACC | 53 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(50): Show | 53 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.-31+13091_-31+1309 others(6): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55593436 | |||||
chr14:55593445
|
C | CA | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+13091_-31+1309 others(5): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55593445 | ||||||
chr14:55593446
|
C | A | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+13092C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55593446 | ||||||
chr14:55593447
|
A | C | 9 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(6): Show | 9 | HG02622.hp1 HG02723.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31+13093A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55593447 | ||||||
chr14:55593593
|
G | A | 2 | a0001c0001t0001g0296a0001c0001t0001g0299 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-31+13239G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55593593 | ||||||
chr14:55593671
|
C | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+13317C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55593671 | ||||||
chr14:55593723
|
T | G | 97 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0142others(94): Show | 97 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.-31+13369T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55593723 | ||||||
chr14:55593729
|
T | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+13375T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55593729 | ||||||
chr14:55594208
|
GT | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+13860delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55594208 | |||||
chr14:55594354
|
CA | C | 9 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31+14001delA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55594354 | ||||||
chr14:55594498
|
G | GT | 22 | a0001c0001t0001g0004a0001c0001t0001g0118a0001c0001t0001g0119others(19): Show | 22 | HG00597.hp2 HG00639.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.-31+14162dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55594498 | |||||
chr14:55594963
|
G | T | 7 | a0001c0001t0001g0195a0001c0001t0001g0227a0001c0001t0001g0228others(4): Show | 7 | HG01123.hp2 HG01496.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+14609G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55594963 | ||||||
chr14:55595044
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-31+14690A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55595044 | ||||||
chr14:55595066
|
C | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+14712C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55595066 | ||||||
chr14:55595098
|
T | C | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-31+14744T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55595098 | ||||||
chr14:55595119
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+14765G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55595119 | ||||||
chr14:55595200
|
A | ATGTTGAA others(14): Show |
22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+14846_-31+1484 others(25): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55595200 | ||||||
chr14:55595201
|
C | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+14847C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55595201 | ||||||
chr14:55595334
|
C | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+14980C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55595334 | ||||||
chr14:55595461
|
C | CAA | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.-31+15108_-31+1510 others(6): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55595461 | |||||
chr14:55595534
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-31+15180T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55595534 | ||||||
chr14:55595614
|
A | G | 1 | a0001c0009t0001g0086 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-31+15260A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55595614 | ||||||
chr14:55595682
|
T | C | 88 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(85): Show | 88 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-31+15328T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55595682 | ||||||
chr14:55595725
|
A | G | 8 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0116others(5): Show | 8 | HG01123.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-31+15371A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55595725 | ||||||
chr14:55595772
|
A | G | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+15418A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55595772 | ||||||
chr14:55595872
|
C | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+15518C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55595872 | ||||||
chr14:55595965
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-31+15611T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55595965 | ||||||
chr14:55595996
|
T | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+15642T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55595996 | ||||||
chr14:55596111
|
T | G | 1 | a0001c0001t0001g0100 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-31+15757T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55596111 | ||||||
chr14:55596154
|
C | CA | 8 | a0001c0001t0001g0122a0001c0001t0001g0159a0001c0001t0001g0165others(5): Show | 8 | HG01123.hp2 HG01993.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.-31+15819dupA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55596154 | |||||
chr14:55596154
|
C | CAAAAA | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+15815_-31+1581 others(9): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55596154 | |||||
chr14:55596154
|
C | CAAAAAAA | 87 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(84): Show | 87 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.-31+15813_-31+1581 others(11): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55596154 | |||||
chr14:55596154
|
C | CAAAAAAA others(1): Show |
11 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0038others(8): Show | 11 | HG00639.hp2 HG00642.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31+15812_-31+1581 others(12): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55596154 | |||||
chr14:55596737
|
G | A | 3 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0291 | 3 | NA18989.hp1 NA19056.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-30-15282G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55596737 | ||||||
chr14:55596801
|
C | CT | 20 | a0001c0001t0001g0231a0001c0002t0003g0175a0001c0002t0003g0177others(17): Show | 20 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-30-15205dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55596801 | |||||
chr14:55596886
|
A | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-15133A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55596886 | ||||||
chr14:55596903
|
C | A | 1 | a0012c0013t0001g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-30-15116C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55596903 | ||||||
chr14:55596926
|
A | G | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30-15093A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55596926 | ||||||
chr14:55597035
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-30-14984A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55597035 | ||||||
chr14:55597063
|
G | GA | 8 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(5): Show | 8 | NA18941.hp1 NA18950.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30-14946dupA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55597063 | |||||
chr14:55597063
|
GA | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-14946delA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55597063 | |||||
chr14:55597072
|
A | C | 2 | a0001c0001t0003g0007a0001c0004t0003g0006 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-30-14947A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55597072 | ||||||
chr14:55597092
|
C | A | 2 | a0001c0001t0002g0079a0001c0001t0002g0080 | 2 | HG01168.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-30-14927C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55597092 | ||||||
chr14:55597315
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-30-14704A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55597315 | ||||||
chr14:55597349
|
G | C | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0123others(1): Show | 4 | HG00673.hp2 HG02080.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-14670G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55597349 | ||||||
chr14:55597406
|
G | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-14613G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55597406 | ||||||
chr14:55597690
|
C | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-14329C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55597690 | ||||||
chr14:55597832
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0245a0001c0001t0001g0278 | 4 | HG00099.hp1 HG01516.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-14187C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55597832 | ||||||
chr14:55597851
|
CA | C | 23 | a0001c0001t0001g0267a0001c0002t0003g0175a0001c0002t0003g0176others(20): Show | 23 | HG00099.hp2 HG00639.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-30-14157delA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55597851 | |||||
chr14:55597983
|
A | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-14036A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55597983 | ||||||
chr14:55598054
|
C | G | 2 | a0002c0003t0003g0192a0002c0003t0003g0194 | 2 | HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30-13965C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55598054 | ||||||
chr14:55598164
|
G | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30-13855G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55598164 | ||||||
chr14:55598192
|
T | G | 1 | a0001c0001t0002g0285 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-30-13827T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55598192 | ||||||
chr14:55598207
|
G | C | 20 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(17): Show | 20 | HG00597.hp2 HG00738.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.-30-13812G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55598207 | ||||||
chr14:55598209
|
G | A | 1 | a0001c0001t0002g0285 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-30-13810G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55598209 | ||||||
chr14:55598296
|
G | A | 2 | a0001c0001t0002g0043a0001c0001t0002g0288 | 2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-30-13723G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55598296 | ||||||
chr14:55598411
|
G | A | 2 | a0001c0001t0002g0017a0001c0001t0002g0018 | 2 | HG02165.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-30-13608G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55598411 | ||||||
chr14:55598434
|
C | CA | 10 | a0001c0001t0001g0233a0001c0001t0001g0309a0001c0001t0004g0280others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-30-13568dupA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55598434 | |||||
chr14:55598449
|
A | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30-13570A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55598449 | ||||||
chr14:55598460
|
G | T | 1 | a0001c0001t0001g0207 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-30-13559G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55598460 | ||||||
chr14:55598464
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-30-13555C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55598464 | ||||||
chr14:55598505
|
T | TA | 85 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(82): Show | 85 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.-30-13503dupA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55598505 | |||||
chr14:55598505
|
TA | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30-13503delA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55598505 | |||||
chr14:55598584
|
G | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30-13435G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55598584 | ||||||
chr14:55598929
|
C | T | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30-13090C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55598929 | ||||||
chr14:55599009
|
A | C | 1 | a0005c0006t0002g0040 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-30-13010A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55599009 | ||||||
chr14:55599060
|
T | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-12959T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55599060 | ||||||
chr14:55599084
|
T | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30-12935T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55599084 | ||||||
chr14:55599229
|
C | T | 2 | a0001c0001t0004g0225a0001c0001t0004g0226 | 2 | NA18981.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-30-12790C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55599229 | ||||||
chr14:55599254
|
T | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-30-12765T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55599254 | ||||||
chr14:55599370
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-12649G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55599370 | ||||||
chr14:55599513
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-30-12506G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55599513 | ||||||
chr14:55599524
|
G | C | 1 | a0001c0001t0001g0135 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-30-12495G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55599524 | ||||||
chr14:55599557
|
A | G | 1 | a0001c0002t0003g0183 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-30-12462A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55599557 | ||||||
chr14:55599569
|
A | AT | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-12448dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55599569 | |||||
chr14:55599652
|
G | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-12367G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55599652 | ||||||
chr14:55599657
|
A | G | 4 | a0001c0001t0001g0109a0006c0008t0003g0187a0006c0008t0003g0188others(1): Show | 4 | HG02896.hp2 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-12362A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55599657 | ||||||
chr14:55599660
|
A | C | 6 | a0001c0001t0001g0087a0001c0001t0001g0095a0001c0001t0001g0096others(3): Show | 6 | HG02970.hp2 HG03195.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30-12359A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55599660 | ||||||
chr14:55599763
|
G | C | 1 | a0001c0001t0002g0011 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-30-12256G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55599763 | ||||||
chr14:55599872
|
T | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-12147T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55599872 | ||||||
chr14:55599934
|
G | T | 1 | a0001c0001t0001g0001 | 2 | HG00099.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-30-12085G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55599934 | ||||||
chr14:55599962
|
A | G | 1 | a0001c0001t0001g0001 | 2 | HG00099.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-30-12057A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55599962 | ||||||
chr14:55600080
|
C | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-11939C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55600080 | ||||||
chr14:55600086
|
C | T | 113 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(110): Show | 113 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.-30-11933C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55600086 | ||||||
chr14:55600251
|
C | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-11768C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55600251 | ||||||
chr14:55600439
|
A | G | 1 | a0002c0003t0003g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-30-11580A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55600439 | ||||||
chr14:55600446
|
C | G | 1 | a0001c0001t0002g0061 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-30-11573C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55600446 | ||||||
chr14:55600572
|
G | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-11447G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55600572 | ||||||
chr14:55600632
|
C | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30-11387C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55600632 | ||||||
chr14:55600663
|
GATTT | G | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30-11355_-30-1135 others(8): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55600663 | ||||||
chr14:55600664
|
A | G | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-30-11355A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55600664 | ||||||
chr14:55600725
|
TGTA | T | 4 | a0001c0001t0003g0007a0001c0004t0003g0003a0001c0004t0003g0005others(1): Show | 4 | HG02723.hp1 HG03516.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-11291_-30-1128 others(7): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55600725 | |||||
chr14:55600820
|
A | AAAAAGTT | 4 | a0003c0016t0003g0190a0003c0019t0003g0189a0006c0008t0003g0187others(1): Show | 4 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-11197_-30-1119 others(11): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55600820 | |||||
chr14:55600876
|
A | AT | 23 | a0001c0001t0001g0270a0001c0002t0003g0175a0001c0002t0003g0176others(20): Show | 23 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.-30-11132dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55600876 | |||||
chr14:55600983
|
G | A | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30-11036G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55600983 | ||||||
chr14:55601545
|
C | T | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30-10474C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55601545 | ||||||
chr14:55601592
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-30-10427C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55601592 | ||||||
chr14:55601630
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-10389G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55601630 | ||||||
chr14:55601659
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-30-10360A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55601659 | ||||||
chr14:55601766
|
C | T | 4 | a0001c0001t0001g0099a0001c0001t0001g0107a0001c0001t0001g0108others(1): Show | 4 | HG01081.hp2 HG01175.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-10253C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55601766 | ||||||
chr14:55601795
|
G | A | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-30-10224G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55601795 | ||||||
chr14:55601803
|
T | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-10216T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55601803 | ||||||
chr14:55601884
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-30-10135C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55601884 | ||||||
chr14:55601937
|
A | T | 2 | a0006c0008t0003g0187a0006c0008t0003g0188 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-30-10082A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55601937 | ||||||
chr14:55602097
|
G | A | 2 | a0006c0008t0003g0187a0006c0008t0003g0188 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-30-9922G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55602097 | ||||||
chr14:55602108
|
C | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0112others(1): Show | 4 | HG02886.hp2 HG02896.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-9911C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55602108 | ||||||
chr14:55602136
|
C | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-9883C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55602136 | ||||||
chr14:55602409
|
A | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-9610A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55602409 | ||||||
chr14:55602450
|
G | A | 26 | a0001c0001t0003g0007a0001c0002t0003g0175a0001c0002t0003g0176others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.-30-9569G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55602450 | ||||||
chr14:55602506
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-9513G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55602506 | ||||||
chr14:55602585
|
C | CT | 28 | a0001c0001t0001g0240a0001c0001t0001g0306a0001c0001t0002g0038others(25): Show | 28 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.-30-9420dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55602585 | |||||
chr14:55602755
|
A | G | 2 | a0003c0016t0003g0190a0003c0019t0003g0189 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-30-9264A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55602755 | ||||||
chr14:55602781
|
A | G | 5 | a0001c0002t0003g0179a0001c0002t0003g0180a0001c0002t0003g0181others(2): Show | 5 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30-9238A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55602781 | ||||||
chr14:55602819
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-9200G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55602819 | ||||||
chr14:55602905
|
G | C | 4 | a0001c0009t0001g0084a0001c0009t0001g0086a0009c0014t0001g0172others(1): Show | 4 | HG03540.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-9114G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55602905 | ||||||
chr14:55602928
|
C | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30-9091C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55602928 | ||||||
chr14:55602945
|
C | A | 1 | a0001c0001t0002g0043 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-30-9074C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55602945 | ||||||
chr14:55603012
|
T | C | 5 | a0001c0001t0001g0090a0001c0001t0001g0130a0001c0001t0001g0131others(2): Show | 5 | NA18950.hp1 NA18974.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30-9007T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55603012 | ||||||
chr14:55603065
|
G | A | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30-8954G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55603065 | ||||||
chr14:55603080
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-30-8939T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55603080 | ||||||
chr14:55603166
|
AT | A | 24 | a0001c0001t0001g0146a0001c0001t0002g0044a0001c0002t0003g0175others(21): Show | 24 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.-30-8842delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55603166 | |||||
chr14:55603321
|
C | T | 1 | a0001c0001t0003g0022 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-30-8698C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55603321 | ||||||
chr14:55603331
|
T | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-8688T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55603331 | ||||||
chr14:55603595
|
A | G | 1 | a0001c0001t0002g0285 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-30-8424A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55603595 | ||||||
chr14:55604005
|
G | C | 1 | a0001c0001t0002g0028 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-30-8014G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55604005 | ||||||
chr14:55604257
|
T | C | 2 | a0001c0001t0002g0043a0001c0001t0002g0288 | 2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-30-7762T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55604257 | ||||||
chr14:55604458
|
A | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-7561A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55604458 | ||||||
chr14:55604485
|
A | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-7534A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55604485 | ||||||
chr14:55604499
|
A | C | 1 | a0001c0001t0001g0224 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-30-7520A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55604499 | ||||||
chr14:55604512
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-30-7507G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55604512 | ||||||
chr14:55604721
|
CAAATGAA others(129): Show |
C | 2 | a0001c0001t0001g0296a0001c0001t0001g0299 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-30-7297_-30-7162d others(2): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55604721 | ||||||
chr14:55604728
|
A | G | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30-7291A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55604728 | ||||||
chr14:55604788
|
G | C | 2 | a0002c0003t0003g0192a0002c0003t0003g0194 | 2 | HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30-7231G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55604788 | ||||||
chr14:55604821
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-30-7198A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55604821 | ||||||
chr14:55604895
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-30-7124T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55604895 | ||||||
chr14:55604969
|
C | G | 1 | a0001c0001t0002g0288 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-30-7050C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55604969 | ||||||
chr14:55605003
|
A | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-7016A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55605003 | ||||||
chr14:55605150
|
A | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-6869A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55605150 | ||||||
chr14:55605337
|
G | C | 89 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(86): Show | 89 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.-30-6682G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55605337 | ||||||
chr14:55605368
|
C | A | 19 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0100others(16): Show | 19 | HG01074.hp1 HG01081.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-30-6651C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55605368 | ||||||
chr14:55605860
|
C | A | 1 | a0012c0013t0001g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-30-6159C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55605860 | ||||||
chr14:55605925
|
C | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-6094C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55605925 | ||||||
chr14:55605968
|
T | A | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30-6051T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55605968 | ||||||
chr14:55605970
|
A | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-30-6049A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55605970 | ||||||
chr14:55606078
|
T | C | 1 | a0001c0001t0002g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-30-5941T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55606078 | ||||||
chr14:55606210
|
T | C | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0171 | 3 | HG02109.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-30-5809T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55606210 | ||||||
chr14:55606341
|
T | C | 1 | a0001c0001t0002g0045 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-30-5678T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55606341 | ||||||
chr14:55606443
|
T | C | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30-5576T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55606443 | ||||||
chr14:55606448
|
A | G | 1 | a0001c0001t0002g0016 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-30-5571A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55606448 | ||||||
chr14:55606476
|
A | G | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30-5543A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55606476 | ||||||
chr14:55606488
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-5531G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55606488 | ||||||
chr14:55606513
|
A | G | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30-5506A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55606513 | ||||||
chr14:55606599
|
A | AG | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-5420_-30-5419i others(3): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55606599 | ||||||
chr14:55606762
|
A | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-5257A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55606762 | ||||||
chr14:55607014
|
G | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-5005G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55607014 | ||||||
chr14:55607284
|
C | T | 2 | a0001c0001t0002g0057a0001c0001t0002g0058 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-30-4735C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55607284 | ||||||
chr14:55607290
|
C | G | 2 | a0001c0001t0001g0296a0001c0001t0001g0299 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-30-4729C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55607290 | ||||||
chr14:55607356
|
A | G | 88 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(85): Show | 88 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-30-4663A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55607356 | ||||||
chr14:55607397
|
A | T | 1 | a0001c0001t0001g0305 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-30-4622A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55607397 | ||||||
chr14:55607409
|
C | T | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30-4610C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55607409 | ||||||
chr14:55607417
|
T | C | 89 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(86): Show | 89 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.-30-4602T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55607417 | ||||||
chr14:55607437
|
C | CCTT | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-4580_-30-4579i others(5): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55607437 | |||||
chr14:55607493
|
C | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-4526C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55607493 | ||||||
chr14:55607533
|
C | G | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30-4486C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55607533 | ||||||
chr14:55607560
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-4459G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55607560 | ||||||
chr14:55607992
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-30-4027C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55607992 | ||||||
chr14:55608048
|
T | C | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-30-3971T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55608048 | ||||||
chr14:55608241
|
A | G | 2 | a0003c0016t0003g0190a0003c0019t0003g0189 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-30-3778A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55608241 | ||||||
chr14:55608363
|
A | G | 1 | a0001c0001t0002g0290 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-30-3656A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55608363 | ||||||
chr14:55608624
|
CT | C | 24 | a0001c0001t0001g0004a0001c0001t0002g0023a0001c0002t0003g0175others(21): Show | 24 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.-30-3378delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55608624 | |||||
chr14:55608686
|
C | T | 1 | a0001c0004t0003g0003 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-30-3333C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55608686 | ||||||
chr14:55608786
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-30-3233C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55608786 | ||||||
chr14:55608809
|
T | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-3210T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55608809 | ||||||
chr14:55608882
|
G | A | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30-3137G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55608882 | ||||||
chr14:55609038
|
T | TA | 11 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0227others(8): Show | 11 | HG01123.hp2 HG01496.hp1 NA18965.hp2 others(8): Show |
intron_variant | MODIFIER | c.-30-2968dupA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55609038 | |||||
chr14:55609038
|
TA | T | 22 | a0001c0001t0001g0222a0001c0001t0002g0020a0001c0002t0003g0175others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-2968delA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55609038 | |||||
chr14:55609138
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0002g0289 | 2 | HG02071.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.-30-2881C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55609138 | ||||||
chr14:55609313
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-30-2706C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55609313 | ||||||
chr14:55609467
|
G | C | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30-2552G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55609467 | ||||||
chr14:55609502
|
C | T | 1 | a0003c0019t0003g0189 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-30-2517C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55609502 | ||||||
chr14:55609509
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-30-2510A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55609509 | ||||||
chr14:55609792
|
C | T | 2 | a0003c0016t0003g0190a0003c0019t0003g0189 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-30-2227C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55609792 | ||||||
chr14:55609804
|
A | G | 1 | a0001c0001t0002g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-30-2215A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55609804 | ||||||
chr14:55609832
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-30-2187G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55609832 | ||||||
chr14:55609833
|
ACTGCCCA others(16): Show |
A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-2182_-30-2160d others(25): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55609833 | |||||
chr14:55609931
|
A | G | 1 | a0001c0009t0001g0084 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-30-2088A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55609931 | ||||||
chr14:55610100
|
A | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-1919A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55610100 | ||||||
chr14:55610157
|
T | C | 85 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(82): Show | 85 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.-30-1862T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55610157 | ||||||
chr14:55610214
|
A | G | 9 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30-1805A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55610214 | ||||||
chr14:55610240
|
C | G | 2 | a0003c0016t0003g0190a0003c0019t0003g0189 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-30-1779C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55610240 | ||||||
chr14:55610261
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-30-1758G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55610261 | ||||||
chr14:55610356
|
T | TAA | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-30-1654_-30-1653d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55610356 | |||||
chr14:55610356
|
T | TAAA | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30-1655_-30-1653d others(5): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55610356 | |||||
chr14:55610384
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0020a0001c0001t0002g0021others(68): Show | 71 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.-30-1635C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55610384 | ||||||
chr14:55610400
|
C | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30-1619C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55610400 | ||||||
chr14:55610491
|
C | T | 2 | a0001c0001t0002g0042a0001c0001t0002g0291 | 2 | NA18989.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-30-1528C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55610491 | ||||||
chr14:55610676
|
T | C | 2 | a0003c0016t0003g0190a0003c0019t0003g0189 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-30-1343T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55610676 | ||||||
chr14:55610700
|
A | G | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30-1319A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55610700 | ||||||
chr14:55610714
|
A | AC | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-1305_-30-1304i others(3): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55610714 | ||||||
chr14:55610873
|
T | A | 1 | a0001c0001t0001g0130 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-30-1146T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55610873 | ||||||
chr14:55611243
|
C | T | 86 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0011others(83): Show | 86 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.-30-776C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55611243 | ||||||
chr14:55611246
|
C | T | 5 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0073others(2): Show | 5 | HG00738.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30-773C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55611246 | ||||||
chr14:55611263
|
C | CT | 33 | a0001c0001t0001g0001a0001c0001t0001g0088a0001c0001t0001g0100others(30): Show | 34 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.-30-737dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55611263 | |||||
chr14:55611263
|
CT | C | 15 | a0001c0001t0001g0089a0001c0001t0001g0158a0001c0001t0001g0235others(12): Show | 15 | HG00639.hp2 HG00673.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.-30-737delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55611263 | |||||
chr14:55611263
|
CTTT | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30-739_-30-737del others(3): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr14 | 55611263 | |||||
chr14:55611370
|
G | A | 1 | a0001c0004t0003g0003 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-30-649G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55611370 | ||||||
chr14:55611587
|
G | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0158 | 2 | HG01358.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-30-432G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55611587 | ||||||
chr14:55611712
|
A | G | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30-307A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55611712 | ||||||
chr14:55611734
|
T | C | 309 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(306): Show | 311 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.-30-285T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55611734 | ||||||
chr14:55611835
|
A | T | 1 | a0001c0001t0002g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-30-184A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55611835 | ||||||
chr14:55611978
|
G | T | 1 | a0001c0001t0001g0233 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-30-41G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55611978 | ||||||
chr14:55611981
|
C | CG | 20 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(17): Show | 20 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.-30-38_-30-37insG | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 1/43 | chr14 | 55611981 | ||||||
chr14:55612810
|
T | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.523+239T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55612810 | ||||||
chr14:55612902
|
G | GA | 103 | a0001c0001t0001g0004a0001c0001t0001g0120a0001c0001t0001g0125others(100): Show | 103 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.523+343dupA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr14 | 55612902 | |||||
chr14:55612902
|
GA | G | 21 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(18): Show | 21 | HG00099.hp2 HG00639.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.523+343delA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr14 | 55612902 | |||||
chr14:55612902
|
GAA | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0132others(94): Show | 99 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.523+342_523+343del others(2): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr14 | 55612902 | |||||
chr14:55612923
|
A | C | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.523+352A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55612923 | ||||||
chr14:55612948
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0132others(104): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.523+377A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55612948 | ||||||
chr14:55613008
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0132others(116): Show | 121 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.523+437A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55613008 | ||||||
chr14:55613147
|
G | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0132others(116): Show | 121 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.523+576G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55613147 | ||||||
chr14:55613177
|
A | G | 1 | a0001c0004t0003g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.523+606A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55613177 | ||||||
chr14:55613178
|
C | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.523+607C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55613178 | ||||||
chr14:55613267
|
G | A | 1 | a0009c0014t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.523+696G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55613267 | ||||||
chr14:55613355
|
G | A | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.523+784G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55613355 | ||||||
chr14:55613361
|
A | C | 1 | a0001c0001t0002g0056 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.523+790A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55613361 | ||||||
chr14:55613460
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.523+889G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55613460 | ||||||
chr14:55613491
|
A | AT | 12 | a0001c0001t0001g0114a0001c0001t0001g0129a0001c0001t0001g0222others(9): Show | 12 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.523+939dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr14 | 55613491 | |||||
chr14:55613491
|
AT | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0120a0001c0001t0001g0241others(95): Show | 98 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.523+939delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr14 | 55613491 | |||||
chr14:55613639
|
G | GTGTGCTA others(18): Show |
22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.523+1071_523+1072i others(27): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr14 | 55613639 | |||||
chr14:55613762
|
C | T | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.523+1191C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55613762 | ||||||
chr14:55613824
|
A | T | 1 | a0001c0018t0001g0310 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.523+1253A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55613824 | ||||||
chr14:55613877
|
G | T | 4 | a0003c0016t0003g0190a0003c0019t0003g0189a0006c0008t0003g0187others(1): Show | 4 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+1306G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55613877 | ||||||
chr14:55613901
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.523+1330A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55613901 | ||||||
chr14:55613990
|
T | G | 20 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0100others(17): Show | 20 | HG01074.hp1 HG01081.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.523+1419T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55613990 | ||||||
chr14:55614110
|
A | G | 4 | a0001c0001t0001g0251a0001c0001t0001g0269a0001c0001t0001g0270others(1): Show | 4 | HG00639.hp1 HG01517.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.523+1539A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55614110 | ||||||
chr14:55614301
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.523+1730G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55614301 | ||||||
chr14:55614379
|
A | C | 99 | a0001c0001t0001g0004a0001c0001t0001g0215a0001c0001t0001g0216others(96): Show | 99 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.523+1808A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55614379 | ||||||
chr14:55614411
|
G | A | 3 | a0001c0004t0003g0003a0001c0004t0003g0005a0001c0004t0003g0006 | 3 | HG02723.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.523+1840G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55614411 | ||||||
chr14:55614431
|
G | A | 112 | a0001c0001t0001g0004a0001c0001t0001g0215a0001c0001t0001g0216others(109): Show | 112 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.523+1860G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55614431 | ||||||
chr14:55614519
|
C | T | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.523+1948C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55614519 | ||||||
chr14:55614554
|
A | G | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.524-1963A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55614554 | ||||||
chr14:55614645
|
C | T | 99 | a0001c0001t0001g0004a0001c0001t0001g0215a0001c0001t0001g0216others(96): Show | 99 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.524-1872C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55614645 | ||||||
chr14:55614737
|
G | A | 1 | a0001c0001t0002g0046 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.524-1780G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55614737 | ||||||
chr14:55614757
|
T | G | 108 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(105): Show | 108 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.524-1760T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55614757 | ||||||
chr14:55615286
|
C | A | 1 | a0001c0001t0002g0046 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.524-1231C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55615286 | ||||||
chr14:55615329
|
C | T | 20 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0227others(17): Show | 20 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.524-1188C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55615329 | ||||||
chr14:55615377
|
G | A | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.524-1140G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55615377 | ||||||
chr14:55615392
|
C | A | 4 | a0003c0016t0003g0190a0003c0019t0003g0189a0006c0008t0003g0187others(1): Show | 4 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.524-1125C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55615392 | ||||||
chr14:55615474
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.524-1043G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55615474 | ||||||
chr14:55615567
|
CAAA | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.524-949_524-947del others(3): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55615567 | ||||||
chr14:55615647
|
C | T | 1 | a0001c0001t0003g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.524-870C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55615647 | ||||||
chr14:55615892
|
T | TTCTC | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.524-617_524-614dup others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr14 | 55615892 | |||||
chr14:55615892
|
T | TTCTCTCT others(13): Show |
10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.524-612_524-611ins others(20): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr14 | 55615892 | |||||
chr14:55615945
|
G | T | 81 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0011others(78): Show | 81 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.524-572G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55615945 | ||||||
chr14:55616000
|
C | A | 2 | a0001c0001t0002g0016a0001c0001t0002g0019 | 2 | NA18941.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.524-517C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55616000 | ||||||
chr14:55616001
|
C | G | 4 | a0003c0016t0003g0190a0003c0019t0003g0189a0006c0008t0003g0187others(1): Show | 4 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.524-516C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55616001 | ||||||
chr14:55616043
|
C | T | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.524-474C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55616043 | ||||||
chr14:55616078
|
AT | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.524-431delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr14 | 55616078 | |||||
chr14:55616267
|
A | T | 1 | a0001c0001t0001g0004 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.524-250A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55616267 | ||||||
chr14:55616401
|
A | G | 19 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0195others(16): Show | 20 | HG00544.hp2 HG01123.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.524-116A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 2/43 | chr14 | 55616401 | ||||||
chr14:55616774
|
A | C | 2 | a0001c0004t0003g0005a0001c0004t0003g0006 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.661+120A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 3/43 | chr14 | 55616774 | ||||||
chr14:55616776
|
TAC | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.661+123_661+124del others(2): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 3/43 | chr14 | 55616776 | ||||||
chr14:55616967
|
T | G | 4 | a0001c0009t0001g0084a0001c0009t0001g0086a0009c0014t0001g0172others(1): Show | 4 | HG03540.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.661+313T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 3/43 | chr14 | 55616967 | ||||||
chr14:55617199
|
A | G | 1 | a0001c0004t0003g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.661+545A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 3/43 | chr14 | 55617199 | ||||||
chr14:55617294
|
A | G | 2 | a0006c0008t0003g0187a0006c0008t0003g0188 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.661+640A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 3/43 | chr14 | 55617294 | ||||||
chr14:55617788
|
G | A | 1 | a0001c0001t0002g0044 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.662-176G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 3/43 | chr14 | 55617788 | ||||||
chr14:55617934
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.662-30A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 3/43 | chr14 | 55617934 | ||||||
chr14:55618197
|
GTCATAGA others(10): Show |
G | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.832+71_832+87delTT others(15): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr14 | 55618197 | |||||
chr14:55618412
|
C | T | 8 | a0001c0001t0001g0259a0001c0001t0001g0262a0001c0001t0001g0263others(5): Show | 8 | HG00642.hp2 HG01070.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.832+278C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 4/43 | chr14 | 55618412 | ||||||
chr14:55618417
|
G | GT | 11 | a0001c0002t0003g0175a0001c0004t0003g0003a0002c0003t0003g0191others(8): Show | 11 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.832+292dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr14 | 55618417 | |||||
chr14:55618654
|
G | A | 3 | a0001c0009t0001g0084a0001c0009t0001g0086a0011c0015t0001g0085 | 3 | HG03540.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.832+520G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 4/43 | chr14 | 55618654 | ||||||
chr14:55618682
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.833-500G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 4/43 | chr14 | 55618682 | ||||||
chr14:55618703
|
G | A | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.833-479G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 4/43 | chr14 | 55618703 | ||||||
chr14:55618852
|
T | A | 6 | a0001c0001t0001g0088a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG01109.hp2 HG01433.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.833-330T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 4/43 | chr14 | 55618852 | ||||||
chr14:55618912
|
AT | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.833-261delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr14 | 55618912 | |||||
chr14:55618930
|
G | A | 2 | a0006c0008t0003g0187a0006c0008t0003g0188 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.833-252G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 4/43 | chr14 | 55618930 | ||||||
chr14:55618931
|
G | A | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.833-251G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 4/43 | chr14 | 55618931 | ||||||
chr14:55619062
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.833-120C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 4/43 | chr14 | 55619062 | ||||||
chr14:55619094
|
G | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(305): Show | 310 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.833-88G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 4/43 | chr14 | 55619094 | ||||||
chr14:55619329
|
A | G | 1 | a0001c0001t0002g0015 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.963+17A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55619329 | ||||||
chr14:55619472
|
T | C | 119 | a0001c0001t0001g0004a0001c0001t0001g0299a0001c0001t0002g0008others(116): Show | 119 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.963+160T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55619472 | ||||||
chr14:55619483
|
C | T | 1 | a0001c0009t0001g0086 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.963+171C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55619483 | ||||||
chr14:55619540
|
C | T | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+228C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55619540 | ||||||
chr14:55619595
|
A | G | 1 | a0004c0007t0002g0287 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.963+283A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55619595 | ||||||
chr14:55619596
|
C | T | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.963+284C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55619596 | ||||||
chr14:55619812
|
A | C | 1 | a0001c0001t0001g0234 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.963+500A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55619812 | ||||||
chr14:55619950
|
C | T | 4 | a0003c0016t0003g0190a0003c0019t0003g0189a0006c0008t0003g0187others(1): Show | 4 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+638C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55619950 | ||||||
chr14:55619962
|
A | T | 3 | a0001c0004t0003g0003a0001c0004t0003g0005a0001c0004t0003g0006 | 3 | HG02723.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.963+650A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55619962 | ||||||
chr14:55620022
|
T | G | 86 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(83): Show | 86 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.963+710T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55620022 | ||||||
chr14:55620023
|
G | GGGCT | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.963+712_963+713ins others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | INFO_REALIGN_3_PRIME | chr14 | 55620023 | |||||
chr14:55620044
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.963+732G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55620044 | ||||||
chr14:55620172
|
C | G | 119 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(116): Show | 119 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.963+860C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55620172 | ||||||
chr14:55620172
|
C | T | 51 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(48): Show | 51 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.963+860C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55620172 | ||||||
chr14:55620335
|
G | A | 3 | a0001c0001t0001g0105a0001c0001t0001g0110a0001c0001t0001g0295 | 3 | HG01074.hp1 HG02055.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.963+1023G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55620335 | ||||||
chr14:55620343
|
A | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+1031A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55620343 | ||||||
chr14:55620430
|
T | G | 119 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(116): Show | 119 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.963+1118T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55620430 | ||||||
chr14:55620706
|
C | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+1394C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55620706 | ||||||
chr14:55620825
|
G | C | 4 | a0003c0016t0003g0190a0003c0019t0003g0189a0006c0008t0003g0187others(1): Show | 4 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+1513G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55620825 | ||||||
chr14:55620851
|
C | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.963+1539C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55620851 | ||||||
chr14:55620990
|
A | C | 1 | a0001c0001t0001g0137 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.963+1678A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55620990 | ||||||
chr14:55620995
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.963+1683G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55620995 | ||||||
chr14:55621073
|
G | A | 109 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.963+1761G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55621073 | ||||||
chr14:55621091
|
A | G | 1 | a0011c0015t0001g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.963+1779A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55621091 | ||||||
chr14:55621199
|
T | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.963+1887T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55621199 | ||||||
chr14:55621255
|
A | G | 1 | a0009c0014t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.963+1943A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55621255 | ||||||
chr14:55621305
|
G | GCTC | 207 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0088others(204): Show | 207 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.963+1994_963+1996d others(5): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | INFO_REALIGN_3_PRIME | chr14 | 55621305 | |||||
chr14:55621346
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.963+2034C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55621346 | ||||||
chr14:55621347
|
G | A | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+2035G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55621347 | ||||||
chr14:55621487
|
G | A | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.963+2175G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55621487 | ||||||
chr14:55621675
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.963+2363C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55621675 | ||||||
chr14:55621676
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.963+2364G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55621676 | ||||||
chr14:55621680
|
C | T | 1 | a0001c0001t0002g0286 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.963+2368C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55621680 | ||||||
chr14:55621684
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.963+2372G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55621684 | ||||||
chr14:55621685
|
G | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.963+2373G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55621685 | ||||||
chr14:55621846
|
CT | C | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 113 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.963+2554delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | INFO_REALIGN_3_PRIME | chr14 | 55621846 | |||||
chr14:55621846
|
CTT | C | 88 | a0001c0001t0001g0004a0001c0001t0001g0139a0001c0001t0002g0009others(85): Show | 88 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.963+2553_963+2554d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | INFO_REALIGN_3_PRIME | chr14 | 55621846 | |||||
chr14:55621848
|
T | C | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.963+2536T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55621848 | ||||||
chr14:55621892
|
A | T | 1 | a0001c0001t0001g0097 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.963+2580A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55621892 | ||||||
chr14:55622142
|
C | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+2830C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55622142 | ||||||
chr14:55622268
|
T | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+2956T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55622268 | ||||||
chr14:55622326
|
G | T | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.963+3014G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55622326 | ||||||
chr14:55622337
|
G | A | 87 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(84): Show | 87 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.963+3025G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55622337 | ||||||
chr14:55622440
|
A | G | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+3128A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55622440 | ||||||
chr14:55622640
|
C | T | 86 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(83): Show | 86 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.963+3328C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55622640 | ||||||
chr14:55622703
|
A | T | 1 | a0001c0001t0001g0221 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.963+3391A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55622703 | ||||||
chr14:55623057
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.963+3745C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55623057 | ||||||
chr14:55623149
|
C | T | 2 | a0003c0016t0003g0190a0003c0019t0003g0189 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.963+3837C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55623149 | ||||||
chr14:55623187
|
A | C | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.963+3875A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55623187 | ||||||
chr14:55623213
|
G | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.963+3901G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55623213 | ||||||
chr14:55623272
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.963+3960A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55623272 | ||||||
chr14:55623320
|
T | A | 1 | a0001c0001t0002g0008 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.963+4008T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55623320 | ||||||
chr14:55623641
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-4271G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55623641 | ||||||
chr14:55623861
|
A | C | 1 | a0001c0001t0001g0214 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.964-4051A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55623861 | ||||||
chr14:55624016
|
A | G | 4 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0112others(1): Show | 4 | HG02886.hp2 HG02896.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-3896A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55624016 | ||||||
chr14:55624061
|
T | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-3851T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55624061 | ||||||
chr14:55624070
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0158 | 2 | HG01358.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.964-3842C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55624070 | ||||||
chr14:55624110
|
T | C | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.964-3802T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55624110 | ||||||
chr14:55624127
|
G | A | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.964-3785G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55624127 | ||||||
chr14:55624187
|
A | G | 1 | a0001c0001t0002g0289 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.964-3725A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55624187 | ||||||
chr14:55624247
|
C | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-3665C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55624247 | ||||||
chr14:55624345
|
T | G | 2 | a0001c0001t0001g0089a0001c0001t0001g0158 | 2 | HG01358.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.964-3567T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55624345 | ||||||
chr14:55624521
|
A | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-3391A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55624521 | ||||||
chr14:55624679
|
A | C | 4 | a0001c0001t0001g0221a0001c0001t0001g0261a0001c0001t0001g0265others(1): Show | 4 | HG00423.hp1 HG03831.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-3233A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55624679 | ||||||
chr14:55624726
|
C | T | 1 | a0001c0001t0002g0285 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.964-3186C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55624726 | ||||||
chr14:55624904
|
G | C | 1 | a0001c0001t0002g0037 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.964-3008G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55624904 | ||||||
chr14:55624954
|
G | A | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.964-2958G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55624954 | ||||||
chr14:55625043
|
A | G | 1 | a0001c0004t0003g0003 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.964-2869A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55625043 | ||||||
chr14:55625079
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.964-2833G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55625079 | ||||||
chr14:55625123
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-2789G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55625123 | ||||||
chr14:55625130
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.964-2782C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55625130 | ||||||
chr14:55625159
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.964-2753A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55625159 | ||||||
chr14:55625251
|
TA | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-2660delA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55625251 | ||||||
chr14:55625255
|
A | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-2657A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55625255 | ||||||
chr14:55625256
|
A | AGTCCC | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-2656_964-2655i others(7): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55625256 | ||||||
chr14:55625667
|
T | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-2245T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55625667 | ||||||
chr14:55625701
|
A | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-2211A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55625701 | ||||||
chr14:55625732
|
GT | G | 4 | a0001c0001t0001g0132a0001c0001t0001g0205a0001c0001t0001g0229others(1): Show | 4 | NA18966.hp1 NA18967.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-2177delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | INFO_REALIGN_3_PRIME | chr14 | 55625732 | |||||
chr14:55625833
|
G | A | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.964-2079G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55625833 | ||||||
chr14:55625839
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.964-2073C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55625839 | ||||||
chr14:55625865
|
C | T | 3 | a0001c0004t0003g0003a0001c0004t0003g0005a0001c0004t0003g0006 | 3 | HG02723.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.964-2047C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55625865 | ||||||
chr14:55625895
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.964-2017A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55625895 | ||||||
chr14:55625937
|
C | G | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.964-1975C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55625937 | ||||||
chr14:55625986
|
A | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-1926A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55625986 | ||||||
chr14:55626001
|
A | G | 86 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(83): Show | 86 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.964-1911A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55626001 | ||||||
chr14:55626092
|
G | A | 3 | a0001c0004t0003g0003a0001c0004t0003g0005a0001c0004t0003g0006 | 3 | HG02723.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.964-1820G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55626092 | ||||||
chr14:55626208
|
C | CA | 14 | a0001c0001t0001g0099a0001c0002t0003g0175a0001c0002t0003g0176others(11): Show | 14 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.964-1693dupA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | INFO_REALIGN_3_PRIME | chr14 | 55626208 | |||||
chr14:55626279
|
T | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-1633T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55626279 | ||||||
chr14:55626409
|
G | A | 1 | a0001c0004t0003g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.964-1503G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55626409 | ||||||
chr14:55626577
|
C | CTGTTT | 6 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.964-1314_964-1310d others(7): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | INFO_REALIGN_3_PRIME | chr14 | 55626577 | |||||
chr14:55626577
|
CTGTTT | C | 4 | a0003c0016t0003g0190a0003c0019t0003g0189a0006c0008t0003g0187others(1): Show | 4 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-1314_964-1310d others(7): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | INFO_REALIGN_3_PRIME | chr14 | 55626577 | |||||
chr14:55626747
|
G | A | 4 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0112others(1): Show | 4 | HG02886.hp2 HG02896.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-1165G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55626747 | ||||||
chr14:55626781
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.964-1131G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55626781 | ||||||
chr14:55626866
|
C | CT | 86 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(83): Show | 86 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.964-1037dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | INFO_REALIGN_3_PRIME | chr14 | 55626866 | |||||
chr14:55626876
|
C | T | 121 | a0001c0001t0001g0004a0001c0001t0001g0296a0001c0001t0001g0299others(118): Show | 121 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.964-1036C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55626876 | ||||||
chr14:55626967
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-945G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55626967 | ||||||
chr14:55627081
|
A | G | 4 | a0003c0016t0003g0190a0003c0019t0003g0189a0006c0008t0003g0187others(1): Show | 4 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-831A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55627081 | ||||||
chr14:55627161
|
C | A | 1 | a0001c0001t0001g0299 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.964-751C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55627161 | ||||||
chr14:55627205
|
C | T | 1 | a0001c0004t0003g0003 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.964-707C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55627205 | ||||||
chr14:55627240
|
G | A | 97 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(94): Show | 97 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.964-672G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55627240 | ||||||
chr14:55627253
|
C | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-659C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55627253 | ||||||
chr14:55627254
|
C | T | 1 | a0001c0001t0005g0070 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.964-658C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55627254 | ||||||
chr14:55627316
|
A | G | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.964-596A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55627316 | ||||||
chr14:55627414
|
A | G | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.964-498A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55627414 | ||||||
chr14:55627519
|
A | C | 1 | a0001c0001t0001g0129 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.964-393A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55627519 | ||||||
chr14:55627615
|
G | A | 4 | a0001c0001t0001g0090a0001c0001t0001g0130a0001c0001t0001g0131others(1): Show | 4 | NA18950.hp1 NA18974.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-297G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55627615 | ||||||
chr14:55627772
|
C | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-140C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55627772 | ||||||
chr14:55627826
|
G | T | 1 | a0001c0001t0001g0001 | 2 | HG00099.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.964-86G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 5/43 | chr14 | 55627826 | ||||||
chr14:55628048
|
C | T | 4 | a0003c0016t0003g0190a0003c0019t0003g0189a0006c0008t0003g0187others(1): Show | 4 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080+20C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55628048 | ||||||
chr14:55628273
|
C | G | 1 | a0009c0014t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1080+245C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55628273 | ||||||
chr14:55628275
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1080+247G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55628275 | ||||||
chr14:55628328
|
A | G | 3 | a0001c0009t0001g0084a0001c0009t0001g0086a0011c0015t0001g0085 | 3 | HG03540.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1080+300A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55628328 | ||||||
chr14:55628395
|
C | T | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1080+367C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55628395 | ||||||
chr14:55628424
|
T | G | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1080+396T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55628424 | ||||||
chr14:55628564
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1080+536T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55628564 | ||||||
chr14:55628758
|
A | T | 1 | a0001c0001t0001g0138 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1080+730A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55628758 | ||||||
chr14:55628787
|
CAT | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1080+761_1080+762d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr14 | 55628787 | |||||
chr14:55629021
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1081-936C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55629021 | ||||||
chr14:55629105
|
T | C | 2 | a0002c0003t0003g0193a0002c0003t0003g0301 | 2 | HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1081-852T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55629105 | ||||||
chr14:55629127
|
G | T | 1 | a0001c0001t0003g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1081-830G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55629127 | ||||||
chr14:55629354
|
C | T | 1 | a0011c0015t0001g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1081-603C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55629354 | ||||||
chr14:55629417
|
C | CA | 18 | a0001c0001t0001g0094a0001c0001t0001g0146a0001c0001t0001g0215others(15): Show | 18 | HG02056.hp1 HG02145.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1081-517dupA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr14 | 55629417 | |||||
chr14:55629417
|
C | CAAAAA | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1081-521_1081-517d others(7): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr14 | 55629417 | |||||
chr14:55629417
|
CA | C | 14 | a0001c0001t0001g0135a0001c0001t0001g0238a0001c0001t0001g0254others(11): Show | 14 | HG01884.hp1 HG02257.hp1 HG03195.hp2 others(11): Show |
intron_variant | MODIFIER | c.1081-517delA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr14 | 55629417 | |||||
chr14:55629455
|
A | G | 20 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(17): Show | 20 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1081-502A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55629455 | ||||||
chr14:55629456
|
G | A | 2 | a0003c0016t0003g0190a0003c0019t0003g0189 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1081-501G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55629456 | ||||||
chr14:55629511
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1081-446G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55629511 | ||||||
chr14:55629616
|
G | C | 1 | a0001c0001t0001g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1081-341G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55629616 | ||||||
chr14:55629711
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1081-246G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55629711 | ||||||
chr14:55629812
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1081-145A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55629812 | ||||||
chr14:55629929
|
T | A | 9 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1081-28T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 6/43 | chr14 | 55629929 | ||||||
chr14:55630410
|
T | A | 109 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1221+313T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55630410 | ||||||
chr14:55630422
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1221+325T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55630422 | ||||||
chr14:55630522
|
G | A | 1 | a0009c0014t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1221+425G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55630522 | ||||||
chr14:55630596
|
A | G | 1 | a0001c0001t0001g0001 | 2 | HG00099.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1221+499A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55630596 | ||||||
chr14:55630744
|
C | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1221+647C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55630744 | ||||||
chr14:55630774
|
C | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1221+677C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55630774 | ||||||
chr14:55630850
|
G | A | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1221+753G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55630850 | ||||||
chr14:55630891
|
A | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | NA18951.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1221+794A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55630891 | ||||||
chr14:55630919
|
G | A | 8 | a0001c0001t0001g0121a0001c0001t0001g0164a0001c0001t0001g0165others(5): Show | 8 | HG02109.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1221+822G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55630919 | ||||||
chr14:55630978
|
T | C | 1 | a0003c0019t0003g0189 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1221+881T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55630978 | ||||||
chr14:55631111
|
TC | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1221+1015delC | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55631111 | ||||||
chr14:55631180
|
C | G | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1221+1083C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55631180 | ||||||
chr14:55631322
|
C | T | 81 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0011others(78): Show | 81 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1221+1225C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55631322 | ||||||
chr14:55631341
|
G | GAGAT | 3 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0194 | 3 | HG01884.hp1 HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1221+1245_1221+124 others(8): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GAGATAGA others(7): Show |
11 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(8): Show | 11 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1221+1245_1221+124 others(18): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GAGATAGA others(11): Show |
1 | a0001c0002t0003g0300 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1221+1245_1221+124 others(22): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GAT | 31 | a0001c0001t0001g0088a0001c0001t0001g0101a0001c0001t0001g0102others(28): Show | 31 | HG00597.hp1 HG01070.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1221+1271_1221+127 others(6): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATAT | 6 | a0001c0001t0001g0133a0001c0001t0001g0198a0001c0001t0001g0204others(3): Show | 6 | HG01123.hp1 HG01243.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1221+1269_1221+127 others(8): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATATAT | 17 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0099others(14): Show | 17 | HG01168.hp1 HG01169.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1221+1267_1221+127 others(10): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATATATA others(1): Show |
8 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0130others(5): Show | 8 | HG02071.hp2 HG02293.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1221+1265_1221+127 others(12): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATATATA others(3): Show |
16 | a0001c0001t0001g0093a0001c0001t0001g0097a0001c0001t0001g0098others(13): Show | 16 | HG00423.hp2 HG01070.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.1221+1263_1221+127 others(14): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATATATA others(5): Show |
10 | a0001c0001t0001g0094a0001c0001t0001g0122a0001c0001t0001g0131others(7): Show | 10 | HG00738.hp1 HG01071.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1221+1261_1221+127 others(16): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATATATA others(7): Show |
6 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0140others(3): Show | 6 | HG01981.hp2 HG02572.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1221+1259_1221+127 others(18): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATATATA others(9): Show |
3 | a0001c0001t0001g0124a0001c0001t0001g0159a0001c0001t0001g0171 | 3 | HG00673.hp2 HG01993.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1221+1257_1221+127 others(20): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATATATA others(13): Show |
1 | a0001c0001t0001g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1221+1253_1221+127 others(24): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATATATA others(19): Show |
1 | a0001c0001t0001g0087 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1221+1247_1221+127 others(30): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATATATA others(21): Show |
2 | a0001c0001t0001g0095a0001c0001t0001g0114 | 2 | NA18522.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1221+1245_1221+127 others(32): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATATATA others(23): Show |
3 | a0001c0009t0001g0084a0009c0014t0001g0172a0010c0011t0005g0173 | 3 | HG03225.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1221+1272_1221+127 others(34): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATTGATA others(1): Show |
37 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0014others(34): Show | 37 | HG00323.hp1 HG01168.hp2 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.1221+1246_1221+124 others(12): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATTGATA others(3): Show |
24 | a0001c0001t0002g0015a0001c0001t0002g0021a0001c0001t0002g0026others(21): Show | 24 | HG00544.hp1 HG00642.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.1221+1246_1221+124 others(14): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATTGATA others(5): Show |
5 | a0001c0001t0002g0012a0001c0001t0002g0033a0001c0001t0002g0039others(2): Show | 5 | HG00558.hp1 HG03834.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.1221+1246_1221+124 others(16): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATTGATA others(7): Show |
4 | a0001c0001t0002g0038a0001c0001t0002g0076a0001c0001t0002g0083others(1): Show | 4 | HG03491.hp2 HG03492.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.1221+1246_1221+124 others(18): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATTGATA others(11): Show |
2 | a0001c0001t0002g0020a0007c0017t0002g0030 | 2 | HG02738.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1221+1246_1221+124 others(22): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATTGATA others(13): Show |
2 | a0001c0001t0002g0025a0001c0001t0002g0285 | 2 | HG00558.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1221+1246_1221+124 others(24): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATTGATA others(15): Show |
1 | a0001c0001t0002g0024 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1221+1246_1221+124 others(26): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATTGATA others(17): Show |
1 | a0001c0001t0002g0066 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1221+1246_1221+124 others(28): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATTGATA others(19): Show |
1 | a0001c0001t0002g0067 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1221+1246_1221+124 others(30): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATTGATA others(21): Show |
1 | a0001c0001t0002g0068 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1221+1246_1221+124 others(32): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
G | GATTGATA others(23): Show |
1 | a0001c0001t0002g0065 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1221+1246_1221+124 others(34): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
GAT | G | 11 | a0001c0001t0001g0089a0001c0001t0001g0096a0001c0001t0001g0106others(8): Show | 11 | HG01358.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1221+1271_1221+127 others(6): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
GATATATA others(7): Show |
G | 4 | a0003c0016t0003g0190a0003c0019t0003g0189a0006c0008t0003g0187others(1): Show | 4 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1221+1259_1221+127 others(18): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631341
|
GATATATA others(9): Show |
G | 10 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(7): Show | 10 | HG00597.hp2 NA18963.hp2 NA18985.hp1 others(7): Show |
intron_variant | MODIFIER | c.1221+1257_1221+127 others(20): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55631341 | |||||
chr14:55631343
|
T | G | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1221+1246T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55631343 | ||||||
chr14:55631347
|
T | G | 2 | a0002c0003t0003g0193a0002c0003t0003g0301 | 2 | HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1221+1250T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55631347 | ||||||
chr14:55631357
|
T | G | 4 | a0003c0016t0003g0190a0003c0019t0003g0189a0006c0008t0003g0187others(1): Show | 4 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1221+1260T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55631357 | ||||||
chr14:55631673
|
C | T | 80 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0011others(77): Show | 80 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.1222-1562C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55631673 | ||||||
chr14:55631712
|
G | A | 5 | a0001c0001t0001g0088a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 5 | HG01109.hp2 HG01433.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222-1523G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55631712 | ||||||
chr14:55631748
|
G | C | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222-1487G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55631748 | ||||||
chr14:55631750
|
C | T | 1 | a0010c0011t0005g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1222-1485C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55631750 | ||||||
chr14:55631901
|
C | A | 1 | a0001c0001t0001g0278 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1222-1334C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55631901 | ||||||
chr14:55632136
|
A | G | 4 | a0003c0016t0003g0190a0003c0019t0003g0189a0006c0008t0003g0187others(1): Show | 4 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222-1099A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55632136 | ||||||
chr14:55632171
|
A | C | 3 | a0001c0009t0001g0084a0001c0009t0001g0086a0011c0015t0001g0085 | 3 | HG03540.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1222-1064A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55632171 | ||||||
chr14:55632365
|
TTA | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1222-869_1222-868d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55632365 | ||||||
chr14:55632370
|
A | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1222-865A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55632370 | ||||||
chr14:55632428
|
C | A | 1 | a0001c0001t0001g0302 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1222-807C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55632428 | ||||||
chr14:55632554
|
G | A | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0018t0001g0310 | 3 | HG01071.hp1 HG01192.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1222-681G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55632554 | ||||||
chr14:55632597
|
GGA | G | 113 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(110): Show | 113 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1222-633_1222-632d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr14 | 55632597 | |||||
chr14:55633110
|
G | T | 21 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(18): Show | 21 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.1222-125G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 7/43 | chr14 | 55633110 | ||||||
chr14:55633360
|
T | A | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1328+19T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | chr14 | 55633360 | ||||||
chr14:55633369
|
A | G | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1328+28A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | chr14 | 55633369 | ||||||
chr14:55633442
|
G | T | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.1328+101G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | chr14 | 55633442 | ||||||
chr14:55633530
|
CTA | C | 6 | a0001c0001t0001g0087a0001c0001t0001g0095a0001c0001t0001g0097others(3): Show | 6 | HG02970.hp1 HG03195.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1328+191_1328+192d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr14 | 55633530 | |||||
chr14:55633618
|
G | A | 2 | a0006c0008t0003g0187a0006c0008t0003g0188 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1328+277G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | chr14 | 55633618 | ||||||
chr14:55633773
|
G | A | 1 | a0003c0016t0003g0190 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1328+432G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | chr14 | 55633773 | ||||||
chr14:55633794
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1328+453A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | chr14 | 55633794 | ||||||
chr14:55633856
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1328+515G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | chr14 | 55633856 | ||||||
chr14:55634048
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1329-478C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | chr14 | 55634048 | ||||||
chr14:55634066
|
A | G | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.1329-460A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | chr14 | 55634066 | ||||||
chr14:55634128
|
C | T | 7 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1329-398C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | chr14 | 55634128 | ||||||
chr14:55634129
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1329-397G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | chr14 | 55634129 | ||||||
chr14:55634159
|
A | T | 2 | a0003c0016t0003g0190a0003c0019t0003g0189 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1329-367A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | chr14 | 55634159 | ||||||
chr14:55634218
|
C | T | 1 | a0002c0003t0003g0193 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1329-308C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | chr14 | 55634218 | ||||||
chr14:55634219
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | NA18971.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1329-307C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | chr14 | 55634219 | ||||||
chr14:55634254
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1329-272C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | chr14 | 55634254 | ||||||
chr14:55634446
|
AAACT | A | 91 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(88): Show | 91 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1329-76_1329-73del others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr14 | 55634446 | |||||
chr14:55634449
|
C | T | 1 | a0003c0019t0003g0189 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1329-77C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | chr14 | 55634449 | ||||||
chr14:55634494
|
C | T | 91 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(88): Show | 91 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1329-32C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 8/43 | chr14 | 55634494 | ||||||
chr14:55634777
|
T | C | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1461+119T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 9/43 | chr14 | 55634777 | ||||||
chr14:55634931
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1461+273G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 9/43 | chr14 | 55634931 | ||||||
chr14:55634977
|
A | T | 1 | a0001c0001t0002g0020 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1461+319A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 9/43 | chr14 | 55634977 | ||||||
chr14:55635161
|
G | A | 87 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(84): Show | 87 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1461+503G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 9/43 | chr14 | 55635161 | ||||||
chr14:55635216
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0003g0007 | 2 | HG02071.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1461+558A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 9/43 | chr14 | 55635216 | ||||||
chr14:55635301
|
A | T | 113 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(110): Show | 113 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1461+643A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 9/43 | chr14 | 55635301 | ||||||
chr14:55635381
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1461+723A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 9/43 | chr14 | 55635381 | ||||||
chr14:55635422
|
C | G | 1 | a0001c0001t0001g0119 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1461+764C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 9/43 | chr14 | 55635422 | ||||||
chr14:55635506
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1461+848G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 9/43 | chr14 | 55635506 | ||||||
chr14:55635703
|
A | C | 1 | a0001c0001t0003g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1462-746A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 9/43 | chr14 | 55635703 | ||||||
chr14:55635946
|
C | G | 14 | a0001c0002t0003g0175a0001c0009t0001g0084a0001c0009t0001g0086others(11): Show | 14 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1462-503C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 9/43 | chr14 | 55635946 | ||||||
chr14:55636010
|
G | A | 1 | a0001c0002t0003g0177 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1462-439G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 9/43 | chr14 | 55636010 | ||||||
chr14:55636015
|
G | A | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1462-434G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 9/43 | chr14 | 55636015 | ||||||
chr14:55636044
|
C | G | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1462-405C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 9/43 | chr14 | 55636044 | ||||||
chr14:55636064
|
A | T | 1 | a0001c0001t0001g0137 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1462-385A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 9/43 | chr14 | 55636064 | ||||||
chr14:55636148
|
A | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG00673.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1462-301A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 9/43 | chr14 | 55636148 | ||||||
chr14:55636254
|
G | T | 2 | a0006c0008t0003g0187a0006c0008t0003g0188 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1462-195G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 9/43 | chr14 | 55636254 | ||||||
chr14:55636595
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1549+59C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 10/43 | chr14 | 55636595 | ||||||
chr14:55636643
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1549+107A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 10/43 | chr14 | 55636643 | ||||||
chr14:55636794
|
T | G | 51 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(48): Show | 51 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.1549+258T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 10/43 | chr14 | 55636794 | ||||||
chr14:55636801
|
T | G | 1 | a0001c0004t0003g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1549+265T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 10/43 | chr14 | 55636801 | ||||||
chr14:55637048
|
G | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1550-150G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 10/43 | chr14 | 55637048 | ||||||
chr14:55637154
|
A | C | 11 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(8): Show | 11 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1550-44A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 10/43 | chr14 | 55637154 | ||||||
chr14:55637164
|
A | G | 54 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0195others(51): Show | 55 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1550-34A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 10/43 | chr14 | 55637164 | ||||||
chr14:55637377
|
CT | C | 16 | a0001c0001t0001g0243a0001c0001t0001g0265a0001c0001t0001g0308others(13): Show | 16 | HG00099.hp2 HG01081.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1716+26delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 11/43 | INFO_REALIGN_3_PRIME | chr14 | 55637377 | |||||
chr14:55637390
|
T | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0097others(21): Show | 25 | HG00099.hp1 HG00639.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1716+26T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 11/43 | chr14 | 55637390 | ||||||
chr14:55637560
|
T | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1716+196T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 11/43 | chr14 | 55637560 | ||||||
chr14:55638033
|
G | T | 88 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(85): Show | 88 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.1785+186G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 12/43 | chr14 | 55638033 | ||||||
chr14:55638225
|
G | A | 103 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(100): Show | 103 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1785+378G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 12/43 | chr14 | 55638225 | ||||||
chr14:55638308
|
A | G | 1 | a0010c0011t0005g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1785+461A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 12/43 | chr14 | 55638308 | ||||||
chr14:55638308
|
A | T | 2 | a0001c0001t0001g0296a0001c0001t0001g0299 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1785+461A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 12/43 | chr14 | 55638308 | ||||||
chr14:55638352
|
C | G | 1 | a0001c0002t0003g0184 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1785+505C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 12/43 | chr14 | 55638352 | ||||||
chr14:55638574
|
A | AT | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1786-606dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr14 | 55638574 | |||||
chr14:55638699
|
A | T | 2 | a0003c0016t0003g0190a0003c0019t0003g0189 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1786-486A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 12/43 | chr14 | 55638699 | ||||||
chr14:55638741
|
A | T | 53 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(50): Show | 53 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.1786-444A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 12/43 | chr14 | 55638741 | ||||||
chr14:55638760
|
A | C | 4 | a0001c0009t0001g0084a0001c0009t0001g0086a0009c0014t0001g0172others(1): Show | 4 | HG03540.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1786-425A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 12/43 | chr14 | 55638760 | ||||||
chr14:55638832
|
T | A | 90 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(87): Show | 90 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.1786-353T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 12/43 | chr14 | 55638832 | ||||||
chr14:55638976
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0025 | 2 | HG00558.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1786-209A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 12/43 | chr14 | 55638976 | ||||||
chr14:55639295
|
T | C | 53 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(50): Show | 53 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.1823+73T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 13/43 | chr14 | 55639295 | ||||||
chr14:55639313
|
TGAC | T | 98 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(95): Show | 98 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.1823+95_1823+97del others(3): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 13/43 | INFO_REALIGN_3_PRIME | chr14 | 55639313 | |||||
chr14:55639362
|
C | CT | 21 | a0001c0001t0001g0095a0001c0001t0001g0124a0001c0001t0001g0129others(18): Show | 21 | HG00639.hp2 HG00673.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1823+157dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 13/43 | INFO_REALIGN_3_PRIME | chr14 | 55639362 | |||||
chr14:55639362
|
CT | C | 106 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(103): Show | 106 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.1823+157delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 13/43 | INFO_REALIGN_3_PRIME | chr14 | 55639362 | |||||
chr14:55639493
|
G | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(95): Show | 98 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.1823+271G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 13/43 | chr14 | 55639493 | ||||||
chr14:55640050
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1914+47T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 14/43 | chr14 | 55640050 | ||||||
chr14:55640066
|
G | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1914+63G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 14/43 | chr14 | 55640066 | ||||||
chr14:55640149
|
C | A | 3 | a0001c0001t0001g0105a0001c0001t0001g0110a0001c0001t0001g0295 | 3 | HG01074.hp1 HG02055.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1914+146C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 14/43 | chr14 | 55640149 | ||||||
chr14:55640159
|
C | G | 1 | a0001c0001t0002g0290 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1914+156C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 14/43 | chr14 | 55640159 | ||||||
chr14:55640196
|
A | G | 2 | a0001c0001t0004g0208a0001c0001t0004g0209 | 2 | NA18986.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1915-178A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 14/43 | chr14 | 55640196 | ||||||
chr14:55640222
|
A | G | 1 | a0001c0009t0001g0086 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1915-152A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 14/43 | chr14 | 55640222 | ||||||
chr14:55640333
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1915-41G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 14/43 | chr14 | 55640333 | ||||||
chr14:55640489
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1983+47C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 15/43 | chr14 | 55640489 | ||||||
chr14:55640556
|
A | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1983+114A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 15/43 | chr14 | 55640556 | ||||||
chr14:55640558
|
C | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1983+116C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 15/43 | chr14 | 55640558 | ||||||
chr14:55640685
|
T | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | NA18951.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1983+243T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 15/43 | chr14 | 55640685 | ||||||
chr14:55641098
|
T | G | 1 | a0001c0001t0002g0059 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2022-29T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 16/43 | chr14 | 55641098 | ||||||
chr14:55641289
|
G | A | 97 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(94): Show | 97 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.2103+81G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 17/43 | chr14 | 55641289 | ||||||
chr14:55641315
|
G | A | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.2103+107G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 17/43 | chr14 | 55641315 | ||||||
chr14:55641399
|
G | A | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2103+191G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 17/43 | chr14 | 55641399 | ||||||
chr14:55641483
|
C | G | 3 | a0001c0001t0002g0045a0001c0001t0002g0054a0001c0001t0002g0063 | 3 | NA18998.hp1 NA19003.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2104-209C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 17/43 | chr14 | 55641483 | ||||||
chr14:55641571
|
C | T | 4 | a0003c0016t0003g0190a0003c0019t0003g0189a0006c0008t0003g0187others(1): Show | 4 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2104-121C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 17/43 | chr14 | 55641571 | ||||||
chr14:55641764
|
A | T | 1 | a0001c0004t0003g0003 | 1 | NA19043.hp1 | splice_region_variant&intron_variant | LOW | c.2172+4A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55641764 | ||||||
chr14:55641802
|
A | G | 97 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(94): Show | 97 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.2172+42A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55641802 | ||||||
chr14:55641868
|
G | C | 2 | a0004c0007t0002g0013a0004c0007t0002g0287 | 2 | HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2172+108G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55641868 | ||||||
chr14:55641881
|
T | C | 2 | a0003c0016t0003g0190a0003c0019t0003g0189 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2172+121T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55641881 | ||||||
chr14:55641898
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2172+138C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55641898 | ||||||
chr14:55642040
|
T | G | 1 | a0001c0001t0001g0224 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2172+280T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55642040 | ||||||
chr14:55642051
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2172+291C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55642051 | ||||||
chr14:55642125
|
T | A | 1 | a0001c0001t0001g0255 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2172+365T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55642125 | ||||||
chr14:55642351
|
A | G | 4 | a0001c0009t0001g0084a0001c0009t0001g0086a0009c0014t0001g0172others(1): Show | 4 | HG03540.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2172+591A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55642351 | ||||||
chr14:55642441
|
A | T | 1 | a0001c0001t0002g0047 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2172+681A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55642441 | ||||||
chr14:55642456
|
A | G | 99 | a0001c0001t0001g0004a0001c0001t0001g0239a0001c0001t0001g0240others(96): Show | 99 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.2172+696A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55642456 | ||||||
chr14:55642487
|
T | G | 2 | a0001c0001t0001g0296a0001c0001t0001g0299 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2172+727T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55642487 | ||||||
chr14:55642779
|
A | T | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2172+1019A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55642779 | ||||||
chr14:55642861
|
G | T | 2 | a0004c0007t0002g0013a0004c0007t0002g0287 | 2 | HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2172+1101G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55642861 | ||||||
chr14:55642921
|
T | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2172+1161T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55642921 | ||||||
chr14:55643062
|
A | G | 1 | a0001c0001t0001g0002 | 2 | HG02080.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.2172+1302A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55643062 | ||||||
chr14:55643096
|
G | C | 51 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(48): Show | 51 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.2172+1336G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55643096 | ||||||
chr14:55643150
|
T | G | 1 | a0003c0019t0003g0189 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2172+1390T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55643150 | ||||||
chr14:55643291
|
C | G | 7 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0112others(4): Show | 7 | HG01243.hp1 HG02109.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2172+1531C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55643291 | ||||||
chr14:55643542
|
A | C | 1 | a0001c0001t0001g0004 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2172+1782A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55643542 | ||||||
chr14:55643547
|
T | C | 22 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0099others(19): Show | 22 | HG01074.hp1 HG01081.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2172+1787T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55643547 | ||||||
chr14:55643590
|
T | C | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.2172+1830T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55643590 | ||||||
chr14:55643821
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0132others(96): Show | 101 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2172+2061G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55643821 | ||||||
chr14:55643868
|
T | C | 1 | a0001c0001t0002g0044 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2172+2108T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55643868 | ||||||
chr14:55643876
|
T | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.2172+2116T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55643876 | ||||||
chr14:55644054
|
C | A | 1 | a0001c0001t0001g0004 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2172+2294C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55644054 | ||||||
chr14:55644087
|
A | G | 20 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0100others(17): Show | 20 | HG01074.hp1 HG01081.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2172+2327A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55644087 | ||||||
chr14:55644298
|
A | G | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.2172+2538A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55644298 | ||||||
chr14:55644384
|
A | C | 21 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0099others(18): Show | 21 | HG01074.hp1 HG01081.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2173-2589A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55644384 | ||||||
chr14:55644560
|
C | CT | 19 | a0001c0001t0001g0095a0001c0001t0001g0099a0001c0001t0001g0115others(16): Show | 19 | HG00423.hp1 HG01109.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2173-2394dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55644560 | |||||
chr14:55644560
|
CT | C | 108 | a0001c0001t0001g0004a0001c0001t0001g0146a0001c0001t0001g0213others(105): Show | 108 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.2173-2394delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55644560 | |||||
chr14:55644621
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2173-2352A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55644621 | ||||||
chr14:55644682
|
A | G | 87 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0002g0008others(84): Show | 87 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.2173-2291A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55644682 | ||||||
chr14:55644735
|
A | G | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.2173-2238A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55644735 | ||||||
chr14:55644819
|
A | C | 1 | a0001c0001t0002g0047 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2173-2154A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55644819 | ||||||
chr14:55644850
|
A | G | 98 | a0001c0001t0001g0004a0001c0001t0001g0239a0001c0001t0001g0240others(95): Show | 98 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.2173-2123A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55644850 | ||||||
chr14:55644890
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2173-2083C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55644890 | ||||||
chr14:55644989
|
G | A | 120 | a0001c0001t0001g0004a0001c0001t0001g0239a0001c0001t0001g0240others(117): Show | 120 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.2173-1984G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55644989 | ||||||
chr14:55645056
|
T | C | 1 | a0001c0001t0003g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2173-1917T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55645056 | ||||||
chr14:55645436
|
C | T | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.2173-1537C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55645436 | ||||||
chr14:55645672
|
C | T | 1 | a0001c0001t0002g0288 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2173-1301C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55645672 | ||||||
chr14:55645717
|
G | A | 1 | a0001c0001t0003g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2173-1256G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55645717 | ||||||
chr14:55645745
|
C | A | 89 | a0001c0001t0001g0004a0001c0001t0001g0239a0001c0001t0001g0240others(86): Show | 89 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.2173-1228C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55645745 | ||||||
chr14:55645842
|
A | C | 1 | a0001c0001t0002g0033 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2173-1131A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55645842 | ||||||
chr14:55645962
|
G | C | 1 | a0001c0001t0001g0163 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2173-1011G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55645962 | ||||||
chr14:55646004
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0312 | 2 | HG01934.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2173-969G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646004 | ||||||
chr14:55646027
|
C | G | 2 | a0003c0016t0003g0190a0003c0019t0003g0189 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2173-946C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646027 | ||||||
chr14:55646041
|
G | C | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.2173-932G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646041 | ||||||
chr14:55646090
|
TGGACATA others(19): Show |
T | 7 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2173-878_2173-853d others(28): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646090 | |||||
chr14:55646249
|
T | C | 3 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0002g0012 | 3 | HG00558.hp1 NA18963.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2173-724T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646249 | ||||||
chr14:55646356
|
G | GAA | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2173-610_2173-609d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646356 | |||||
chr14:55646391
|
GTCTT | G | 3 | a0001c0001t0001g0170a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | HG03490.hp2 HG03492.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2173-569_2173-566d others(6): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646391 | |||||
chr14:55646427
|
CTTCCT | C | 6 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0155others(3): Show | 6 | HG01099.hp1 NA18985.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.2173-533_2173-529d others(7): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646427 | |||||
chr14:55646427
|
CTTCCTTT others(27): Show |
C | 1 | a0011c0015t0001g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2173-528_2173-495d others(36): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646427 | |||||
chr14:55646431
|
CTTTCCTT others(22): Show |
C | 4 | a0001c0001t0003g0022a0001c0009t0001g0084a0001c0009t0001g0086others(1): Show | 4 | HG06807.hp1 NA18906.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.2173-528_2173-500d others(31): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646431 | |||||
chr14:55646436
|
C | CTTTCCT | 12 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0098others(9): Show | 13 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2173-510_2173-505d others(8): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646436 | |||||
chr14:55646436
|
C | CTTTCCTT others(5): Show |
2 | a0001c0001t0001g0087a0001c0001t0001g0095 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2173-516_2173-505d others(14): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646436 | |||||
chr14:55646436
|
C | CTTTCCTT others(17): Show |
1 | a0001c0001t0001g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2173-528_2173-505d others(26): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646436 | |||||
chr14:55646436
|
CTTTCCT | C | 5 | a0001c0001t0001g0088a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 5 | HG01109.hp2 HG01433.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.2173-510_2173-505d others(8): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646436 | |||||
chr14:55646441
|
CT | C | 72 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0011others(69): Show | 72 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.2173-528delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646441 | |||||
chr14:55646441
|
CTTTTCCT others(12): Show |
C | 3 | a0001c0001t0002g0048a0001c0001t0002g0285a0001c0001t0002g0288 | 3 | HG01099.hp2 HG01993.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2173-528_2173-510d others(21): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646441 | |||||
chr14:55646442
|
T | TTTCC | 12 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2173-529_2173-528i others(6): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646442 | |||||
chr14:55646442
|
T | TTTCCTTT others(2): Show |
3 | a0001c0001t0002g0034a0001c0001t0002g0046a0001c0002t0003g0183 | 3 | HG01943.hp2 NA18612.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2173-529_2173-528i others(11): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646442 | |||||
chr14:55646442
|
T | TTTCCTTT others(7): Show |
1 | a0001c0001t0002g0290 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2173-529_2173-528i others(16): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646442 | |||||
chr14:55646443
|
T | TTCC | 5 | a0001c0001t0002g0035a0001c0001t0002g0068a0001c0001t0002g0071others(2): Show | 5 | HG02165.hp1 HG02738.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.2173-529_2173-528i others(5): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646443 | |||||
chr14:55646444
|
TTC | T | 10 | a0001c0001t0001g0004a0001c0001t0003g0007a0001c0004t0003g0003others(7): Show | 10 | HG01884.hp1 HG02071.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2173-528_2173-527d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646444 | ||||||
chr14:55646445
|
T | C | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2173-528T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646445 | ||||||
chr14:55646446
|
C | T | 5 | a0001c0001t0002g0035a0001c0001t0002g0068a0001c0001t0002g0071others(2): Show | 5 | HG02165.hp1 HG02738.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.2173-527C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646446 | ||||||
chr14:55646447
|
C | T | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2173-526C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646447 | ||||||
chr14:55646448
|
T | C | 15 | a0001c0001t0001g0004a0001c0001t0002g0035a0001c0001t0002g0068others(12): Show | 15 | HG01884.hp1 HG02071.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.2173-525T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646448 | ||||||
chr14:55646450
|
TTC | T | 69 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0011others(66): Show | 69 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.2173-522_2173-521d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646450 | ||||||
chr14:55646452
|
C | T | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2173-521C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646452 | ||||||
chr14:55646454
|
T | C | 71 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0002g0008others(68): Show | 71 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.2173-519T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646454 | ||||||
chr14:55646454
|
T | TTTTCTTT others(47): Show |
1 | a0001c0001t0001g0157 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2173-515_2173-514i others(56): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646454 | |||||
chr14:55646458
|
C | CCCTTTCC others(13): Show |
2 | a0001c0001t0001g0253a0001c0001t0001g0257 | 2 | NA18952.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2173-514_2173-513i others(22): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646458 | |||||
chr14:55646460
|
T | C | 12 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(9): Show | 12 | HG02055.hp2 HG04199.hp1 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.2173-513T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646460 | ||||||
chr14:55646460
|
T | TTTTCC | 25 | a0001c0001t0001g0002a0001c0001t0001g0099a0001c0001t0001g0101others(22): Show | 26 | HG00423.hp1 HG01071.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.2173-430_2173-426d others(7): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646460
|
T | TTTTCCCT others(29): Show |
1 | a0001c0001t0001g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2173-508_2173-507i others(38): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646460
|
T | TTTTCCTT others(3): Show |
18 | a0001c0001t0001g0088a0001c0001t0001g0118a0001c0001t0001g0120others(15): Show | 18 | HG00544.hp2 HG01884.hp2 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.2173-435_2173-426d others(12): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646460
|
T | TTTTCCTT others(8): Show |
24 | a0001c0001t0001g0094a0001c0001t0001g0107a0001c0001t0001g0127others(21): Show | 24 | HG00597.hp2 HG00639.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.2173-440_2173-426d others(17): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646460
|
T | TTTTCCTT others(13): Show |
17 | a0001c0001t0001g0093a0001c0001t0001g0097a0001c0001t0001g0098others(14): Show | 17 | HG00423.hp2 HG00738.hp1 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.2173-445_2173-426d others(22): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646460
|
T | TTTTCCTT others(18): Show |
8 | a0001c0001t0001g0115a0001c0001t0001g0124a0001c0001t0001g0159others(5): Show | 8 | HG00673.hp2 HG01993.hp2 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.2173-450_2173-426d others(27): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646460
|
T | TTTTCCTT others(23): Show |
7 | a0001c0001t0001g0095a0001c0001t0001g0123a0001c0001t0001g0149others(4): Show | 7 | HG00673.hp1 HG01099.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.2173-455_2173-426d others(32): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646460
|
T | TTTTCCTT others(28): Show |
10 | a0001c0001t0001g0114a0001c0001t0001g0142a0001c0001t0001g0143others(7): Show | 10 | HG01070.hp2 HG01071.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.2173-460_2173-426d others(37): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646460
|
T | TTTTCCTT others(33): Show |
3 | a0001c0001t0001g0156a0001c0001t0001g0198a0001c0001t0009g0260 | 3 | HG00323.hp2 HG03669.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2173-465_2173-426d others(42): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646460
|
T | TTTTCCTT others(38): Show |
3 | a0001c0001t0001g0129a0001c0001t0001g0309a0001c0001t0004g0225 | 3 | HG02738.hp1 NA18981.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2173-470_2173-426d others(47): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646460
|
T | TTTTCCTT others(43): Show |
2 | a0001c0001t0001g0087a0001c0001t0001g0306 | 2 | HG02056.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2173-475_2173-426d others(52): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646460
|
T | TTTTCCTT others(48): Show |
1 | a0013c0010t0001g0144 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2173-480_2173-426d others(57): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646460
|
TTTTCC | T | 27 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0096others(24): Show | 27 | HG00597.hp1 HG01070.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.2173-430_2173-426d others(7): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646460
|
TTTTCCTT others(3): Show |
T | 9 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0105others(6): Show | 9 | HG01074.hp1 HG02300.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.2173-435_2173-426d others(12): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646460
|
TTTTCCTT others(8): Show |
T | 8 | a0001c0001t0001g0091a0001c0001t0001g0150a0001c0001t0001g0151others(5): Show | 8 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.2173-440_2173-426d others(17): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646460
|
TTTTCCTT others(13): Show |
T | 1 | a0012c0013t0001g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2173-445_2173-426d others(22): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646460
|
TTTTCCTT others(18): Show |
T | 3 | a0001c0001t0001g0113a0001c0001t0001g0162a0001c0001t0001g0296 | 3 | HG01243.hp1 HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2173-450_2173-426d others(27): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646460
|
TTTTCCTT others(58): Show |
T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2173-490_2173-426d others(67): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646460 | |||||
chr14:55646463
|
T | TC | 6 | a0001c0001t0002g0035a0001c0001t0002g0068a0001c0001t0002g0071others(3): Show | 6 | HG02165.hp1 HG02723.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.2173-508dupC | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646463 | |||||
chr14:55646464
|
CCTTTCCT others(12): Show |
C | 1 | a0001c0001t0003g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2173-507_2173-489d others(21): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646464 | |||||
chr14:55646464
|
CCTTTCCT others(47): Show |
C | 1 | a0010c0011t0005g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2173-507_2173-454d others(56): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646464 | |||||
chr14:55646466
|
TTTCCTTT others(7): Show |
T | 2 | a0002c0003t0003g0193a0002c0003t0003g0301 | 2 | HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2173-504_2173-491d others(16): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646466 | |||||
chr14:55646466
|
TTTCCTTT others(27): Show |
T | 3 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0194 | 3 | HG01884.hp1 HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2173-504_2173-471d others(36): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646466 | |||||
chr14:55646467
|
TTCC | T | 16 | a0001c0001t0002g0008a0001c0001t0002g0014a0001c0001t0002g0021others(13): Show | 16 | HG00544.hp1 HG01257.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2173-504_2173-502d others(5): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646467 | |||||
chr14:55646467
|
TTCCTTTC others(1): Show |
T | 24 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0002g0015others(21): Show | 24 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.2173-504_2173-497d others(10): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646467 | |||||
chr14:55646467
|
TTCCTTTC others(6): Show |
T | 10 | a0001c0001t0002g0012a0001c0001t0002g0041a0001c0001t0002g0042others(7): Show | 10 | HG00558.hp1 HG01433.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2173-504_2173-492d others(15): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | 55646467 | |||||
chr14:55646468
|
T | TTC | 22 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0002g0024others(19): Show | 22 | HG01346.hp1 HG02071.hp1 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.2173-505_2173-504i others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646468 | ||||||
chr14:55646470
|
C | T | 1 | a0003c0016t0003g0190 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2173-503C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646470 | ||||||
chr14:55646473
|
T | C | 16 | a0001c0001t0002g0008a0001c0001t0002g0014a0001c0001t0002g0021others(13): Show | 16 | HG00544.hp1 HG01257.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2173-500T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646473 | ||||||
chr14:55646474
|
C | T | 2 | a0001c0001t0007g0174a0001c0002t0003g0175 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2173-499C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646474 | ||||||
chr14:55646475
|
C | T | 1 | a0003c0019t0003g0189 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2173-498C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646475 | ||||||
chr14:55646476
|
T | C | 2 | a0001c0001t0007g0174a0001c0002t0003g0175 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2173-497T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646476 | ||||||
chr14:55646478
|
T | C | 24 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0002g0015others(21): Show | 24 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.2173-495T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646478 | ||||||
chr14:55646479
|
C | T | 3 | a0001c0001t0002g0048a0001c0001t0002g0285a0001c0001t0002g0288 | 3 | HG01099.hp2 HG01993.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2173-494C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646479 | ||||||
chr14:55646481
|
T | C | 3 | a0001c0001t0002g0048a0001c0001t0002g0285a0001c0001t0002g0288 | 3 | HG01099.hp2 HG01993.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2173-492T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646481 | ||||||
chr14:55646483
|
T | C | 14 | a0001c0001t0002g0012a0001c0001t0002g0041a0001c0001t0002g0042others(11): Show | 14 | HG00558.hp1 HG01433.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2173-490T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646483 | ||||||
chr14:55646483
|
TCC | T | 3 | a0001c0001t0002g0048a0001c0001t0002g0285a0001c0001t0002g0288 | 3 | HG01099.hp2 HG01993.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2173-489_2173-488d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646483 | ||||||
chr14:55646485
|
C | T | 3 | a0001c0002t0003g0175a0006c0008t0003g0187a0006c0008t0003g0188 | 3 | HG02451.hp1 HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2173-488C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646485 | ||||||
chr14:55646488
|
T | C | 3 | a0001c0001t0002g0048a0001c0001t0002g0285a0001c0001t0002g0288 | 3 | HG01099.hp2 HG01993.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2173-485T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646488 | ||||||
chr14:55646489
|
C | T | 3 | a0001c0001t0003g0022a0001c0009t0001g0084a0001c0009t0001g0086 | 3 | NA18906.hp2 NA18986.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2173-484C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646489 | ||||||
chr14:55646491
|
T | C | 3 | a0001c0001t0003g0022a0001c0009t0001g0084a0001c0009t0001g0086 | 3 | NA18906.hp2 NA18986.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2173-482T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646491 | ||||||
chr14:55646493
|
TCC | T | 3 | a0001c0001t0003g0022a0001c0009t0001g0084a0001c0009t0001g0086 | 3 | NA18906.hp2 NA18986.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2173-479_2173-478d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646493 | ||||||
chr14:55646494
|
C | T | 2 | a0009c0014t0001g0172a0011c0015t0001g0085 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2173-479C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646494 | ||||||
chr14:55646496
|
T | C | 2 | a0009c0014t0001g0172a0011c0015t0001g0085 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2173-477T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646496 | ||||||
chr14:55646498
|
T | C | 3 | a0001c0001t0003g0022a0001c0009t0001g0084a0001c0009t0001g0086 | 3 | NA18906.hp2 NA18986.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2173-475T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646498 | ||||||
chr14:55646503
|
T | C | 2 | a0009c0014t0001g0172a0011c0015t0001g0085 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2173-470T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646503 | ||||||
chr14:55646509
|
C | T | 3 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0194 | 3 | HG01884.hp1 HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2173-464C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646509 | ||||||
chr14:55646511
|
T | C | 4 | a0001c0001t0002g0020a0002c0003t0003g0191a0002c0003t0003g0192others(1): Show | 4 | HG01884.hp1 HG02257.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2173-462T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646511 | ||||||
chr14:55646513
|
TCC | T | 3 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0194 | 3 | HG01884.hp1 HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2173-459_2173-458d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646513 | ||||||
chr14:55646518
|
T | C | 3 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0194 | 3 | HG01884.hp1 HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2173-455T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646518 | ||||||
chr14:55646519
|
C | G | 1 | a0001c0004t0003g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2173-454C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646519 | ||||||
chr14:55646520
|
C | T | 3 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0194 | 3 | HG01884.hp1 HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2173-453C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646520 | ||||||
chr14:55646565
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2173-408T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646565 | ||||||
chr14:55646619
|
G | A | 1 | a0001c0009t0001g0086 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2173-354G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646619 | ||||||
chr14:55646630
|
G | A | 1 | a0001c0001t0002g0034 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2173-343G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646630 | ||||||
chr14:55646732
|
A | T | 93 | a0001c0001t0001g0004a0001c0001t0001g0239a0001c0001t0001g0240others(90): Show | 93 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.2173-241A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646732 | ||||||
chr14:55646789
|
G | A | 93 | a0001c0001t0001g0004a0001c0001t0001g0239a0001c0001t0001g0240others(90): Show | 93 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.2173-184G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646789 | ||||||
chr14:55646870
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2173-103A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | chr14 | 55646870 | ||||||
chr14:55647013
|
A | G | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG00639.hp1 HG03490.hp1 |
splice_region_variant&intron_variant | LOW | c.2207+6A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647013 | ||||||
chr14:55647044
|
T | C | 1 | a0001c0001t0002g0016 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2207+37T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647044 | ||||||
chr14:55647069
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2207+62A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647069 | ||||||
chr14:55647118
|
A | G | 4 | a0001c0004t0003g0003a0001c0004t0003g0005a0001c0004t0003g0006others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2207+111A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647118 | ||||||
chr14:55647160
|
G | A | 2 | a0001c0001t0001g0296a0001c0001t0001g0299 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2207+153G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647160 | ||||||
chr14:55647199
|
A | C | 105 | a0001c0001t0001g0004a0001c0001t0001g0239a0001c0001t0001g0240others(102): Show | 105 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.2207+192A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647199 | ||||||
chr14:55647320
|
C | T | 1 | a0001c0001t0003g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2207+313C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647320 | ||||||
chr14:55647361
|
G | A | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2207+354G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647361 | ||||||
chr14:55647368
|
C | T | 4 | a0001c0009t0001g0084a0001c0009t0001g0086a0009c0014t0001g0172others(1): Show | 4 | HG03540.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2207+361C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647368 | ||||||
chr14:55647398
|
GCTGAGGC others(11): Show |
G | 1 | a0001c0001t0001g0238 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2207+398_2207+415d others(20): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr14 | 55647398 | |||||
chr14:55647548
|
A | G | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(304): Show | 309 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.2208-477A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647548 | ||||||
chr14:55647582
|
G | A | 1 | a0001c0001t0002g0033 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2208-443G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647582 | ||||||
chr14:55647588
|
A | G | 116 | a0001c0001t0001g0004a0001c0001t0001g0239a0001c0001t0001g0240others(113): Show | 116 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.2208-437A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647588 | ||||||
chr14:55647604
|
G | A | 89 | a0001c0001t0001g0004a0001c0001t0001g0239a0001c0001t0001g0240others(86): Show | 89 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.2208-421G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647604 | ||||||
chr14:55647633
|
C | CA | 60 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0098others(57): Show | 60 | HG00597.hp2 HG00673.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.2208-365dupA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr14 | 55647633 | |||||
chr14:55647633
|
CA | C | 12 | a0001c0001t0001g0116a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2208-365delA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr14 | 55647633 | |||||
chr14:55647633
|
CAA | C | 27 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0014others(24): Show | 27 | HG00544.hp1 HG00642.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.2208-366_2208-365d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr14 | 55647633 | |||||
chr14:55647633
|
CAAA | C | 73 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0002g0009others(70): Show | 73 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.2208-367_2208-365d others(5): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr14 | 55647633 | |||||
chr14:55647670
|
A | G | 94 | a0001c0001t0001g0004a0001c0001t0001g0239a0001c0001t0001g0240others(91): Show | 94 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.2208-355A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647670 | ||||||
chr14:55647715
|
C | T | 6 | a0001c0001t0001g0088a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG01109.hp2 HG01433.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.2208-310C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647715 | ||||||
chr14:55647735
|
G | A | 6 | a0001c0001t0002g0048a0001c0001t0002g0077a0001c0001t0002g0082others(3): Show | 6 | HG01099.hp2 NA18946.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.2208-290G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647735 | ||||||
chr14:55647805
|
G | A | 2 | a0006c0008t0003g0187a0006c0008t0003g0188 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2208-220G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647805 | ||||||
chr14:55647812
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2208-213C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647812 | ||||||
chr14:55647948
|
A | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0025 | 2 | HG00558.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2208-77A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647948 | ||||||
chr14:55647955
|
A | G | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2208-70A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 19/43 | chr14 | 55647955 | ||||||
chr14:55648148
|
A | T | 89 | a0001c0001t0001g0004a0001c0001t0001g0239a0001c0001t0001g0240others(86): Show | 89 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.2298+33A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 20/43 | chr14 | 55648148 | ||||||
chr14:55648315
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2298+200T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 20/43 | chr14 | 55648315 | ||||||
chr14:55648350
|
A | T | 1 | a0001c0001t0001g0122 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2298+235A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 20/43 | chr14 | 55648350 | ||||||
chr14:55648479
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2299-323G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 20/43 | chr14 | 55648479 | ||||||
chr14:55648584
|
T | A | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2299-218T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 20/43 | chr14 | 55648584 | ||||||
chr14:55648754
|
A | G | 2 | a0006c0008t0003g0187a0006c0008t0003g0188 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2299-48A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 20/43 | chr14 | 55648754 | ||||||
chr14:55648778
|
T | C | 4 | a0001c0009t0001g0084a0001c0009t0001g0086a0009c0014t0001g0172others(1): Show | 4 | HG03540.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2299-24T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 20/43 | chr14 | 55648778 | ||||||
chr14:55648939
|
T | A | 4 | a0001c0009t0001g0084a0001c0009t0001g0086a0009c0014t0001g0172others(1): Show | 4 | HG03540.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2367+69T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 21/43 | chr14 | 55648939 | ||||||
chr14:55649363
|
T | TTGTA | 115 | a0001c0001t0001g0004a0001c0001t0001g0239a0001c0001t0001g0240others(112): Show | 115 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.2368-411_2368-410i others(6): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 21/43 | INFO_REALIGN_3_PRIME | chr14 | 55649363 | |||||
chr14:55649456
|
C | G | 1 | a0001c0001t0001g0299 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2368-320C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 21/43 | chr14 | 55649456 | ||||||
chr14:55649858
|
AT | A | 114 | a0001c0001t0001g0004a0001c0001t0001g0239a0001c0001t0001g0240others(111): Show | 114 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.2405+55delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr14 | 55649858 | |||||
chr14:55649867
|
T | G | 2 | a0001c0001t0001g0110a0012c0013t0001g0111 | 2 | HG03139.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2405+54T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 22/43 | chr14 | 55649867 | ||||||
chr14:55649954
|
A | G | 2 | a0006c0008t0003g0187a0006c0008t0003g0188 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2405+141A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 22/43 | chr14 | 55649954 | ||||||
chr14:55649994
|
TA | T | 99 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0002g0008others(96): Show | 99 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.2405+194delA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr14 | 55649994 | |||||
chr14:55650005
|
A | C | 3 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0194 | 3 | HG01884.hp1 HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2405+192A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 22/43 | chr14 | 55650005 | ||||||
chr14:55650007
|
A | C | 1 | a0001c0001t0005g0052 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2405+194A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 22/43 | chr14 | 55650007 | ||||||
chr14:55650008
|
C | A | 1 | a0001c0001t0005g0052 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2405+195C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 22/43 | chr14 | 55650008 | ||||||
chr14:55650016
|
A | T | 4 | a0001c0004t0003g0003a0001c0004t0003g0005a0001c0004t0003g0006others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405+203A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 22/43 | chr14 | 55650016 | ||||||
chr14:55650499
|
C | G | 1 | a0001c0001t0002g0290 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2497-70C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 23/43 | chr14 | 55650499 | ||||||
chr14:55650674
|
A | G | 2 | a0001c0001t0004g0208a0001c0001t0004g0209 | 2 | NA18986.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.2565+37A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 24/43 | chr14 | 55650674 | ||||||
chr14:55650751
|
T | C | 1 | a0001c0001t0002g0071 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2565+114T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 24/43 | chr14 | 55650751 | ||||||
chr14:55650833
|
T | G | 10 | a0001c0002t0003g0176a0001c0002t0003g0179a0001c0002t0003g0180others(7): Show | 10 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.2565+196T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 24/43 | chr14 | 55650833 | ||||||
chr14:55650916
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0312 | 2 | HG01934.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2565+279G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 24/43 | chr14 | 55650916 | ||||||
chr14:55650920
|
A | T | 1 | a0001c0004t0003g0003 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2565+283A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 24/43 | chr14 | 55650920 | ||||||
chr14:55650990
|
G | T | 1 | a0001c0001t0001g0309 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2565+353G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 24/43 | chr14 | 55650990 | ||||||
chr14:55651167
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2565+530T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 24/43 | chr14 | 55651167 | ||||||
chr14:55651422
|
C | G | 1 | a0001c0004t0003g0003 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2566-468C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 24/43 | chr14 | 55651422 | ||||||
chr14:55651496
|
G | T | 1 | a0001c0001t0001g0215 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2566-394G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 24/43 | chr14 | 55651496 | ||||||
chr14:55651511
|
A | T | 2 | a0001c0001t0004g0225a0001c0001t0004g0226 | 2 | NA18981.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.2566-379A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 24/43 | chr14 | 55651511 | ||||||
chr14:55651650
|
A | G | 3 | a0001c0009t0001g0084a0001c0009t0001g0086a0011c0015t0001g0085 | 3 | HG03540.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2566-240A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 24/43 | chr14 | 55651650 | ||||||
chr14:55651837
|
A | G | 2 | a0001c0001t0001g0296a0001c0001t0001g0299 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2566-53A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 24/43 | chr14 | 55651837 | ||||||
chr14:55652000
|
T | C | 1 | a0001c0001t0004g0209 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2603+73T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652000 | ||||||
chr14:55652048
|
T | G | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2603+121T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652048 | ||||||
chr14:55652065
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2603+138G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652065 | ||||||
chr14:55652079
|
T | C | 1 | a0002c0003t0003g0191 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2603+152T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652079 | ||||||
chr14:55652183
|
C | G | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2603+256C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652183 | ||||||
chr14:55652393
|
C | CT | 32 | a0001c0001t0001g0094a0001c0001t0001g0099a0001c0001t0001g0126others(29): Show | 32 | HG00423.hp1 HG00597.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.2604-434dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr14 | 55652393 | |||||
chr14:55652393
|
CT | C | 7 | a0001c0001t0001g0108a0001c0001t0001g0114a0001c0001t0001g0150others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2604-434delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr14 | 55652393 | |||||
chr14:55652393
|
CTTT | C | 6 | a0001c0002t0003g0175a0002c0003t0003g0301a0003c0016t0003g0190others(3): Show | 6 | HG00639.hp2 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2604-436_2604-434d others(5): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr14 | 55652393 | |||||
chr14:55652429
|
C | T | 1 | a0001c0001t0002g0069 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2604-421C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652429 | ||||||
chr14:55652437
|
C | T | 11 | a0001c0009t0001g0084a0001c0009t0001g0086a0002c0003t0003g0191others(8): Show | 11 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2604-413C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652437 | ||||||
chr14:55652468
|
G | A | 1 | a0002c0003t0003g0193 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2604-382G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652468 | ||||||
chr14:55652589
|
C | T | 2 | a0001c0002t0003g0176a0001c0002t0003g0300 | 2 | HG01175.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2604-261C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652589 | ||||||
chr14:55652590
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2604-260G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652590 | ||||||
chr14:55652601
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0311 | 2 | HG02071.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.2604-249G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652601 | ||||||
chr14:55652603
|
G | C | 1 | a0001c0001t0002g0285 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2604-247G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652603 | ||||||
chr14:55652606
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0002g0021 | 2 | HG02056.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.2604-244A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652606 | ||||||
chr14:55652614
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2604-236T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652614 | ||||||
chr14:55652620
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0003g0128 | 2 | HG02886.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2604-230T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652620 | ||||||
chr14:55652623
|
T | A | 1 | a0001c0001t0001g0275 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2604-227T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652623 | ||||||
chr14:55652634
|
T | C | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2604-216T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652634 | ||||||
chr14:55652646
|
G | A | 1 | a0001c0001t0003g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2604-204G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652646 | ||||||
chr14:55652650
|
T | C | 2 | a0001c0001t0001g0105a0001c0001t0001g0295 | 2 | HG01074.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.2604-200T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652650 | ||||||
chr14:55652665
|
T | C | 1 | a0001c0001t0002g0049 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2604-185T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652665 | ||||||
chr14:55652672
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2604-178T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652672 | ||||||
chr14:55652683
|
G | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0170a0001c0001t0001g0202 | 3 | HG02970.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2604-167G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652683 | ||||||
chr14:55652688
|
T | C | 2 | a0006c0008t0003g0187a0006c0008t0003g0188 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2604-162T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652688 | ||||||
chr14:55652691
|
G | A | 49 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(46): Show | 49 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.2604-159G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652691 | ||||||
chr14:55652695
|
G | A | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.2604-155G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652695 | ||||||
chr14:55652736
|
C | T | 111 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0002g0008others(108): Show | 111 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.2604-114C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 25/43 | chr14 | 55652736 | ||||||
chr14:55653276
|
C | T | 4 | a0001c0004t0003g0003a0001c0004t0003g0005a0001c0004t0003g0006others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2763+191C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 27/43 | chr14 | 55653276 | ||||||
chr14:55653294
|
A | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | NA18951.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2763+209A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 27/43 | chr14 | 55653294 | ||||||
chr14:55653460
|
T | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2764-99T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 27/43 | chr14 | 55653460 | ||||||
chr14:55653520
|
T | C | 1 | a0001c0001t0002g0059 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2764-39T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 27/43 | chr14 | 55653520 | ||||||
chr14:55653882
|
A | G | 124 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0107others(121): Show | 124 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.2801+286A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 28/43 | chr14 | 55653882 | ||||||
chr14:55654330
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2801+734A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 28/43 | chr14 | 55654330 | ||||||
chr14:55654348
|
A | AAATG | 103 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0107others(100): Show | 103 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2801+753_2801+754i others(6): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 28/43 | INFO_REALIGN_3_PRIME | chr14 | 55654348 | |||||
chr14:55654411
|
A | G | 1 | a0001c0004t0003g0006 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2801+815A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 28/43 | chr14 | 55654411 | ||||||
chr14:55654538
|
AT | A | 26 | a0001c0001t0001g0264a0001c0001t0002g0056a0001c0001t0004g0280others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.2801+956delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 28/43 | INFO_REALIGN_3_PRIME | chr14 | 55654538 | |||||
chr14:55654538
|
ATT | A | 92 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0107others(89): Show | 92 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.2801+955_2801+956d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 28/43 | INFO_REALIGN_3_PRIME | chr14 | 55654538 | |||||
chr14:55654709
|
C | T | 91 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0107others(88): Show | 91 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.2801+1113C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 28/43 | chr14 | 55654709 | ||||||
chr14:55654936
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2802-1106C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 28/43 | chr14 | 55654936 | ||||||
chr14:55655036
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2802-1006T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 28/43 | chr14 | 55655036 | ||||||
chr14:55655193
|
G | A | 1 | a0001c0001t0002g0054 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2802-849G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 28/43 | chr14 | 55655193 | ||||||
chr14:55655440
|
A | G | 4 | a0001c0009t0001g0084a0001c0009t0001g0086a0009c0014t0001g0172others(1): Show | 4 | HG03540.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2802-602A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 28/43 | chr14 | 55655440 | ||||||
chr14:55655443
|
A | G | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2802-599A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 28/43 | chr14 | 55655443 | ||||||
chr14:55655476
|
T | C | 5 | a0001c0001t0002g0292a0001c0004t0003g0003a0001c0004t0003g0005others(2): Show | 5 | HG02145.hp2 HG02723.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2802-566T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 28/43 | chr14 | 55655476 | ||||||
chr14:55655596
|
T | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0107a0001c0001t0001g0108 | 3 | HG01081.hp2 HG01175.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2802-446T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 28/43 | chr14 | 55655596 | ||||||
chr14:55655762
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2802-280T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 28/43 | chr14 | 55655762 | ||||||
chr14:55655895
|
T | A | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.2802-147T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 28/43 | chr14 | 55655895 | ||||||
chr14:55655971
|
G | A | 91 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0107others(88): Show | 91 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.2802-71G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 28/43 | chr14 | 55655971 | ||||||
chr14:55656277
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0257 | 2 | NA18952.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2892+145T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | chr14 | 55656277 | ||||||
chr14:55656311
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2892+179T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | chr14 | 55656311 | ||||||
chr14:55656390
|
T | C | 1 | a0001c0001t0002g0081 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2892+258T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | chr14 | 55656390 | ||||||
chr14:55656606
|
C | T | 2 | a0006c0008t0003g0187a0006c0008t0003g0188 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2892+474C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | chr14 | 55656606 | ||||||
chr14:55656745
|
G | A | 1 | a0009c0014t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2892+613G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | chr14 | 55656745 | ||||||
chr14:55656818
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2892+686G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | chr14 | 55656818 | ||||||
chr14:55657397
|
G | GGTTTTTT others(3): Show |
1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2893-1149_2893-114 others(14): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | chr14 | 55657397 | ||||||
chr14:55657397
|
G | GT | 12 | a0001c0001t0001g0105a0001c0001t0001g0162a0001c0001t0001g0164others(9): Show | 12 | HG00597.hp1 HG01074.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.2893-1135dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr14 | 55657397 | |||||
chr14:55657397
|
G | GTTTTTTT | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2893-1141_2893-113 others(11): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr14 | 55657397 | |||||
chr14:55657397
|
G | GTTTTTTT others(5): Show |
2 | a0006c0008t0003g0187a0006c0008t0003g0188 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2893-1146_2893-113 others(16): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr14 | 55657397 | |||||
chr14:55657397
|
G | GTTTTTTT others(31): Show |
3 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0194 | 3 | HG01884.hp1 HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2893-1137_2893-113 others(42): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr14 | 55657397 | |||||
chr14:55657397
|
G | GTTTTTTT others(19): Show |
1 | a0002c0003t0003g0301 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2893-1136_2893-113 others(30): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr14 | 55657397 | |||||
chr14:55657397
|
G | GTTTTTTT others(22): Show |
1 | a0002c0003t0003g0193 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2893-1136_2893-113 others(33): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr14 | 55657397 | |||||
chr14:55657397
|
G | GTTTTTTT others(8): Show |
1 | a0001c0009t0001g0086 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2893-1135_2893-113 others(19): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr14 | 55657397 | |||||
chr14:55657397
|
G | GTTTTTTT others(10): Show |
1 | a0009c0014t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2893-1135_2893-113 others(21): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr14 | 55657397 | |||||
chr14:55657397
|
GT | G | 85 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0002g0008others(82): Show | 85 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.2893-1135delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr14 | 55657397 | |||||
chr14:55657468
|
T | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2893-1078T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | chr14 | 55657468 | ||||||
chr14:55657610
|
C | T | 4 | a0001c0009t0001g0084a0001c0009t0001g0086a0009c0014t0001g0172others(1): Show | 4 | HG03540.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2893-936C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | chr14 | 55657610 | ||||||
chr14:55657658
|
C | A | 2 | a0001c0001t0002g0069a0001c0001t0005g0070 | 2 | NA18951.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.2893-888C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | chr14 | 55657658 | ||||||
chr14:55657666
|
T | C | 26 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.2893-880T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | chr14 | 55657666 | ||||||
chr14:55657861
|
T | C | 26 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.2893-685T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | chr14 | 55657861 | ||||||
chr14:55657862
|
T | C | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.2893-684T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | chr14 | 55657862 | ||||||
chr14:55657897
|
CAG | C | 3 | a0001c0009t0001g0084a0001c0009t0001g0086a0011c0015t0001g0085 | 3 | HG03540.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2893-648_2893-647d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | chr14 | 55657897 | ||||||
chr14:55657995
|
CTT | C | 14 | a0001c0002t0003g0175a0001c0009t0001g0084a0001c0009t0001g0086others(11): Show | 14 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2893-550_2893-549d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | chr14 | 55657995 | ||||||
chr14:55658312
|
C | G | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2893-234C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | chr14 | 55658312 | ||||||
chr14:55658448
|
A | G | 1 | a0001c0001t0001g0146 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2893-98A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 29/43 | chr14 | 55658448 | ||||||
chr14:55658648
|
C | T | 26 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.2961+34C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 30/43 | chr14 | 55658648 | ||||||
chr14:55658649
|
G | A | 3 | a0001c0004t0003g0003a0001c0004t0003g0005a0001c0004t0003g0006 | 3 | HG02723.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2961+35G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 30/43 | chr14 | 55658649 | ||||||
chr14:55658936
|
A | G | 8 | a0001c0009t0001g0084a0001c0009t0001g0086a0003c0016t0003g0190others(5): Show | 8 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.2961+322A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 30/43 | chr14 | 55658936 | ||||||
chr14:55659049
|
T | TA | 26 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.2961+438dupA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr14 | 55659049 | |||||
chr14:55659053
|
T | A | 26 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.2961+439T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 30/43 | chr14 | 55659053 | ||||||
chr14:55659306
|
T | TG | 9 | a0001c0001t0002g0009a0001c0001t0002g0029a0001c0001t0002g0032others(6): Show | 9 | HG00544.hp1 HG00738.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2962-359dupG | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr14 | 55659306 | |||||
chr14:55659307
|
GT | G | 12 | a0001c0001t0001g0143a0001c0001t0001g0162a0001c0001t0001g0197others(9): Show | 12 | HG01070.hp1 HG01070.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.2962-341delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr14 | 55659307 | |||||
chr14:55659308
|
T | G | 104 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0107others(101): Show | 104 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.2962-358T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 30/43 | chr14 | 55659308 | ||||||
chr14:55659309
|
T | G | 5 | a0001c0001t0002g0058a0001c0001t0002g0078a0001c0002t0003g0182others(2): Show | 5 | HG01256.hp1 HG01516.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2962-357T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 30/43 | chr14 | 55659309 | ||||||
chr14:55659310
|
T | G | 1 | a0001c0004t0003g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2962-356T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 30/43 | chr14 | 55659310 | ||||||
chr14:55659459
|
T | C | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.2962-207T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 30/43 | chr14 | 55659459 | ||||||
chr14:55659480
|
C | A | 119 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0107others(116): Show | 119 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.2962-186C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 30/43 | chr14 | 55659480 | ||||||
chr14:55659516
|
A | T | 1 | a0001c0001t0002g0029 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2962-150A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 30/43 | chr14 | 55659516 | ||||||
chr14:55659608
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2962-58A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 30/43 | chr14 | 55659608 | ||||||
chr14:55659738
|
C | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(305): Show | 310 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.2999+35C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 31/43 | chr14 | 55659738 | ||||||
chr14:55660004
|
G | C | 105 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0107others(102): Show | 105 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.2999+301G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 31/43 | chr14 | 55660004 | ||||||
chr14:55660322
|
A | G | 20 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0032others(17): Show | 20 | HG00544.hp1 HG01099.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.2999+619A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 31/43 | chr14 | 55660322 | ||||||
chr14:55660389
|
G | GT | 12 | a0001c0001t0001g0088a0001c0001t0001g0101a0001c0001t0001g0102others(9): Show | 12 | HG01071.hp1 HG01109.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2999+707dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 31/43 | INFO_REALIGN_3_PRIME | chr14 | 55660389 | |||||
chr14:55660389
|
GT | G | 17 | a0001c0001t0001g0210a0001c0001t0001g0223a0001c0002t0003g0176others(14): Show | 17 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.2999+707delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 31/43 | INFO_REALIGN_3_PRIME | chr14 | 55660389 | |||||
chr14:55660389
|
GTTT | G | 85 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(82): Show | 85 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.2999+705_2999+707d others(5): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 31/43 | INFO_REALIGN_3_PRIME | chr14 | 55660389 | |||||
chr14:55660484
|
T | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2999+781T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 31/43 | chr14 | 55660484 | ||||||
chr14:55660729
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0257 | 2 | NA18952.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.3000-793C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 31/43 | chr14 | 55660729 | ||||||
chr14:55660864
|
G | A | 1 | a0001c0001t0002g0044 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3000-658G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 31/43 | chr14 | 55660864 | ||||||
chr14:55660933
|
T | C | 9 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(6): Show | 9 | HG00597.hp2 NA18963.hp2 NA18985.hp2 others(6): Show |
intron_variant | MODIFIER | c.3000-589T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 31/43 | chr14 | 55660933 | ||||||
chr14:55661173
|
A | G | 2 | a0004c0007t0002g0013a0004c0007t0002g0287 | 2 | HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.3000-349A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 31/43 | chr14 | 55661173 | ||||||
chr14:55661198
|
T | A | 1 | a0009c0014t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3000-324T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 31/43 | chr14 | 55661198 | ||||||
chr14:55661206
|
G | C | 1 | a0001c0001t0001g0219 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3000-316G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 31/43 | chr14 | 55661206 | ||||||
chr14:55661252
|
C | A | 1 | a0001c0001t0001g0303 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3000-270C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 31/43 | chr14 | 55661252 | ||||||
chr14:55661256
|
A | G | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3000-266A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 31/43 | chr14 | 55661256 | ||||||
chr14:55661333
|
T | C | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3000-189T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 31/43 | chr14 | 55661333 | ||||||
chr14:55661665
|
A | C | 9 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.3090+53A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | chr14 | 55661665 | ||||||
chr14:55661669
|
A | G | 4 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0056others(1): Show | 4 | HG02071.hp1 HG02132.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.3090+57A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | chr14 | 55661669 | ||||||
chr14:55661763
|
C | T | 2 | a0006c0008t0003g0187a0006c0008t0003g0188 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3090+151C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | chr14 | 55661763 | ||||||
chr14:55661767
|
G | A | 2 | a0006c0008t0003g0187a0006c0008t0003g0188 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3090+155G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | chr14 | 55661767 | ||||||
chr14:55662069
|
C | CT | 8 | a0001c0001t0001g0146a0001c0001t0001g0166a0001c0002t0003g0175others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.3090+476dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr14 | 55662069 | |||||
chr14:55662069
|
C | CTT | 7 | a0002c0003t0003g0192a0002c0003t0003g0193a0002c0003t0003g0194others(4): Show | 7 | HG02257.hp1 HG03195.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.3090+475_3090+476d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr14 | 55662069 | |||||
chr14:55662069
|
CT | C | 89 | a0001c0001t0001g0004a0001c0001t0001g0212a0001c0001t0001g0266others(86): Show | 89 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.3090+476delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr14 | 55662069 | |||||
chr14:55662069
|
CTT | C | 13 | a0001c0001t0002g0045a0001c0002t0003g0176a0001c0002t0003g0177others(10): Show | 13 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.3090+475_3090+476d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr14 | 55662069 | |||||
chr14:55662148
|
A | C | 99 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(96): Show | 99 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.3090+536A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | chr14 | 55662148 | ||||||
chr14:55662358
|
C | T | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.3090+746C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | chr14 | 55662358 | ||||||
chr14:55662496
|
A | G | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.3090+884A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | chr14 | 55662496 | ||||||
chr14:55662816
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0003g0007 | 2 | HG02071.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3091-1139A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | chr14 | 55662816 | ||||||
chr14:55662936
|
G | A | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.3091-1019G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | chr14 | 55662936 | ||||||
chr14:55662978
|
A | G | 1 | a0001c0001t0002g0067 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3091-977A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | chr14 | 55662978 | ||||||
chr14:55663028
|
T | A | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.3091-927T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | chr14 | 55663028 | ||||||
chr14:55663252
|
A | C | 1 | a0001c0001t0002g0014 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3091-703A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | chr14 | 55663252 | ||||||
chr14:55663358
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3091-597C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | chr14 | 55663358 | ||||||
chr14:55663527
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0295 | 2 | HG01074.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.3091-428A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | chr14 | 55663527 | ||||||
chr14:55663581
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3091-374A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | chr14 | 55663581 | ||||||
chr14:55663851
|
G | T | 5 | a0001c0001t0001g0087a0001c0001t0001g0095a0001c0001t0001g0097others(2): Show | 5 | HG02970.hp1 HG03195.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.3091-104G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 32/43 | chr14 | 55663851 | ||||||
chr14:55664366
|
C | T | 4 | a0001c0009t0001g0084a0001c0009t0001g0086a0009c0014t0001g0172others(1): Show | 4 | HG03540.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3177+325C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55664366 | ||||||
chr14:55664415
|
G | T | 2 | a0001c0002t0003g0183a0001c0002t0003g0184 | 2 | HG01943.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3177+374G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55664415 | ||||||
chr14:55664426
|
C | G | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.3177+385C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55664426 | ||||||
chr14:55664603
|
T | C | 1 | a0001c0001t0001g0258 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.3177+562T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55664603 | ||||||
chr14:55664659
|
T | C | 1 | a0001c0001t0002g0046 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3177+618T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55664659 | ||||||
chr14:55664664
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3177+623C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55664664 | ||||||
chr14:55664759
|
T | G | 1 | a0001c0001t0001g0198 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3177+718T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55664759 | ||||||
chr14:55664909
|
G | A | 3 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0194 | 3 | HG01884.hp1 HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3177+868G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55664909 | ||||||
chr14:55664992
|
AT | A | 97 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0107others(94): Show | 97 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.3177+965delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | INFO_REALIGN_3_PRIME | chr14 | 55664992 | |||||
chr14:55665065
|
A | G | 7 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3177+1024A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55665065 | ||||||
chr14:55665285
|
C | T | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3177+1244C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55665285 | ||||||
chr14:55665861
|
G | C | 4 | a0001c0009t0001g0084a0001c0009t0001g0086a0009c0014t0001g0172others(1): Show | 4 | HG03540.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3178-1380G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55665861 | ||||||
chr14:55666142
|
A | G | 4 | a0001c0004t0003g0003a0001c0004t0003g0005a0001c0004t0003g0006others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3178-1099A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55666142 | ||||||
chr14:55666336
|
C | G | 82 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0011others(79): Show | 82 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.3178-905C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55666336 | ||||||
chr14:55666433
|
T | G | 1 | a0001c0001t0002g0288 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3178-808T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55666433 | ||||||
chr14:55666465
|
G | T | 114 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(111): Show | 114 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.3178-776G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55666465 | ||||||
chr14:55666475
|
C | T | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3178-766C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55666475 | ||||||
chr14:55666533
|
C | T | 1 | a0009c0014t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3178-708C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55666533 | ||||||
chr14:55666758
|
T | G | 2 | a0001c0001t0001g0296a0001c0001t0001g0299 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3178-483T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55666758 | ||||||
chr14:55666775
|
G | A | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.3178-466G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55666775 | ||||||
chr14:55667015
|
T | G | 3 | a0001c0001t0001g0251a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG00639.hp1 HG01517.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.3178-226T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55667015 | ||||||
chr14:55667158
|
A | G | 1 | a0001c0001t0003g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3178-83A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55667158 | ||||||
chr14:55667224
|
C | T | 113 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(110): Show | 113 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.3178-17C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 33/43 | chr14 | 55667224 | ||||||
chr14:55667519
|
ATT | A | 3 | a0001c0001t0002g0045a0001c0001t0002g0054a0001c0001t0002g0063 | 3 | NA18998.hp1 NA19003.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.3267+190_3267+191d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55667519 | ||||||
chr14:55667905
|
CT | C | 88 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(85): Show | 88 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.3267+588delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr14 | 55667905 | |||||
chr14:55667954
|
C | G | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.3267+624C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55667954 | ||||||
chr14:55668037
|
C | G | 87 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(84): Show | 87 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.3267+707C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55668037 | ||||||
chr14:55668331
|
C | T | 87 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(84): Show | 87 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.3267+1001C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55668331 | ||||||
chr14:55668347
|
A | G | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.3267+1017A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55668347 | ||||||
chr14:55668612
|
G | A | 60 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(57): Show | 60 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.3267+1282G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55668612 | ||||||
chr14:55668827
|
C | T | 2 | a0003c0016t0003g0190a0003c0019t0003g0189 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.3267+1497C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55668827 | ||||||
chr14:55668912
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3267+1582A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55668912 | ||||||
chr14:55669372
|
T | G | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG00639.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.3268-1357T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55669372 | ||||||
chr14:55669395
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3268-1334T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55669395 | ||||||
chr14:55669402
|
G | A | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.3268-1327G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55669402 | ||||||
chr14:55669460
|
T | G | 1 | a0010c0011t0005g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3268-1269T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55669460 | ||||||
chr14:55669482
|
A | G | 2 | a0001c0001t0001g0089a0001c0001t0001g0158 | 2 | HG01358.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3268-1247A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55669482 | ||||||
chr14:55669558
|
C | T | 113 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(110): Show | 113 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.3268-1171C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55669558 | ||||||
chr14:55669679
|
A | C | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3268-1050A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55669679 | ||||||
chr14:55669834
|
T | C | 8 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(5): Show | 8 | NA18949.hp2 NA18952.hp2 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.3268-895T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55669834 | ||||||
chr14:55669844
|
C | A | 203 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0088others(200): Show | 203 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.3268-885C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55669844 | ||||||
chr14:55669933
|
A | G | 1 | a0001c0001t0003g0147 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3268-796A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55669933 | ||||||
chr14:55669977
|
G | A | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.3268-752G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55669977 | ||||||
chr14:55670236
|
T | A | 1 | a0001c0001t0001g0162 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3268-493T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55670236 | ||||||
chr14:55670241
|
C | T | 103 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(100): Show | 103 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.3268-488C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55670241 | ||||||
chr14:55670242
|
A | G | 1 | a0009c0014t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3268-487A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55670242 | ||||||
chr14:55670364
|
G | T | 103 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(100): Show | 103 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.3268-365G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55670364 | ||||||
chr14:55670563
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG00099.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3268-166C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55670563 | ||||||
chr14:55670632
|
A | G | 2 | a0006c0008t0003g0187a0006c0008t0003g0188 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3268-97A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55670632 | ||||||
chr14:55670650
|
T | C | 2 | a0001c0004t0003g0005a0001c0004t0003g0006 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3268-79T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55670650 | ||||||
chr14:55670680
|
A | AT | 6 | a0001c0001t0001g0126a0002c0003t0003g0191a0002c0003t0003g0192others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.3268-39dupT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr14 | 55670680 | |||||
chr14:55670689
|
T | C | 4 | a0001c0004t0003g0003a0001c0004t0003g0005a0001c0004t0003g0006others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3268-40T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 34/43 | chr14 | 55670689 | ||||||
chr14:55670836
|
A | G | 1 | a0001c0001t0002g0024 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3348+27A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 35/43 | chr14 | 55670836 | ||||||
chr14:55671022
|
C | T | 2 | a0006c0008t0003g0187a0006c0008t0003g0188 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3348+213C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 35/43 | chr14 | 55671022 | ||||||
chr14:55671057
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3348+248A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 35/43 | chr14 | 55671057 | ||||||
chr14:55671066
|
C | G | 2 | a0006c0008t0003g0187a0006c0008t0003g0188 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3348+257C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 35/43 | chr14 | 55671066 | ||||||
chr14:55671312
|
G | T | 1 | a0006c0008t0003g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3349-254G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 35/43 | chr14 | 55671312 | ||||||
chr14:55671391
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3349-175C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 35/43 | chr14 | 55671391 | ||||||
chr14:55671484
|
C | T | 1 | a0001c0018t0001g0310 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3349-82C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 35/43 | chr14 | 55671484 | ||||||
chr14:55671509
|
G | T | 1 | a0001c0001t0001g0002 | 2 | HG02080.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.3349-57G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 35/43 | chr14 | 55671509 | ||||||
chr14:55671531
|
A | C | 4 | a0001c0004t0003g0003a0001c0004t0003g0005a0001c0004t0003g0006others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3349-35A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 35/43 | chr14 | 55671531 | ||||||
chr14:55671754
|
T | C | 5 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0148others(2): Show | 5 | HG00423.hp2 HG02083.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.3439-31T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 36/43 | chr14 | 55671754 | ||||||
chr14:55671888
|
A | G | 1 | a0001c0001t0002g0029 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3531+11A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 37/43 | chr14 | 55671888 | ||||||
chr14:55672082
|
G | A | 92 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(89): Show | 92 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.3531+205G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 37/43 | chr14 | 55672082 | ||||||
chr14:55672186
|
C | A | 1 | a0003c0016t0003g0190 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3531+309C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 37/43 | chr14 | 55672186 | ||||||
chr14:55672556
|
T | C | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.3532-74T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 37/43 | chr14 | 55672556 | ||||||
chr14:55672583
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3532-47A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 37/43 | chr14 | 55672583 | ||||||
chr14:55672595
|
GT | G | 113 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(110): Show | 113 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.3532-31delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 37/43 | INFO_REALIGN_3_PRIME | chr14 | 55672595 | |||||
chr14:55672764
|
G | A | 3 | a0001c0004t0003g0003a0001c0004t0003g0005a0001c0004t0003g0006 | 3 | HG02723.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3603+63G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 38/43 | chr14 | 55672764 | ||||||
chr14:55672880
|
A | G | 1 | a0001c0009t0001g0086 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3604-49A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 38/43 | chr14 | 55672880 | ||||||
chr14:55673311
|
C | G | 2 | a0001c0004t0003g0005a0001c0004t0003g0006 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3771+56C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55673311 | ||||||
chr14:55673391
|
A | G | 2 | a0001c0004t0003g0005a0001c0004t0003g0006 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3771+136A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55673391 | ||||||
chr14:55673397
|
C | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.3771+142C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55673397 | ||||||
chr14:55673594
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3771+339T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55673594 | ||||||
chr14:55673651
|
T | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.3771+396T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55673651 | ||||||
chr14:55673749
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3771+494C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55673749 | ||||||
chr14:55673924
|
T | C | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3771+669T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55673924 | ||||||
chr14:55673977
|
A | C | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.3771+722A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55673977 | ||||||
chr14:55674113
|
T | C | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3771+858T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55674113 | ||||||
chr14:55674201
|
G | A | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.3771+946G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55674201 | ||||||
chr14:55674262
|
G | A | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3771+1007G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55674262 | ||||||
chr14:55674458
|
G | A | 4 | a0001c0009t0001g0084a0001c0009t0001g0086a0009c0014t0001g0172others(1): Show | 4 | HG03540.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3771+1203G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55674458 | ||||||
chr14:55674611
|
T | A | 1 | a0002c0003t0003g0193 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3772-1224T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55674611 | ||||||
chr14:55674622
|
C | A | 2 | a0001c0001t0002g0065a0001c0001t0002g0066 | 2 | NA18961.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.3772-1213C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55674622 | ||||||
chr14:55674889
|
G | A | 2 | a0001c0001t0001g0296a0001c0001t0001g0299 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3772-946G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55674889 | ||||||
chr14:55675006
|
A | G | 1 | a0001c0001t0002g0290 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3772-829A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55675006 | ||||||
chr14:55675023
|
C | T | 1 | a0001c0001t0002g0041 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3772-812C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55675023 | ||||||
chr14:55675050
|
C | T | 2 | a0001c0001t0002g0027a0001c0001t0002g0290 | 2 | HG01346.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.3772-785C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55675050 | ||||||
chr14:55675319
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3772-516A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55675319 | ||||||
chr14:55675403
|
T | G | 1 | a0001c0001t0001g0130 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3772-432T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55675403 | ||||||
chr14:55675415
|
A | G | 4 | a0001c0009t0001g0084a0001c0009t0001g0086a0009c0014t0001g0172others(1): Show | 4 | HG03540.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3772-420A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55675415 | ||||||
chr14:55675485
|
AAACT | A | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.3772-346_3772-343d others(6): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | INFO_REALIGN_3_PRIME | chr14 | 55675485 | |||||
chr14:55675492
|
C | T | 2 | a0003c0016t0003g0190a0003c0019t0003g0189 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.3772-343C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55675492 | ||||||
chr14:55675553
|
A | G | 5 | a0001c0001t0001g0118a0001c0001t0001g0138a0001c0001t0001g0146others(2): Show | 5 | NA18957.hp2 NA18964.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3772-282A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55675553 | ||||||
chr14:55675762
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0132others(95): Show | 100 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.3772-73A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55675762 | ||||||
chr14:55675831
|
A | G | 2 | a0001c0001t0001g0296a0001c0001t0001g0299 | 2 | HG01243.hp2 HG03098.hp2 |
splice_region_variant&intron_variant | LOW | c.3772-4A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 40/43 | chr14 | 55675831 | ||||||
chr14:55675932
|
G | A | 1 | a0003c0016t0003g0190 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3855+14G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55675932 | ||||||
chr14:55675999
|
T | G | 1 | a0001c0001t0002g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3855+81T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55675999 | ||||||
chr14:55676203
|
C | T | 10 | a0001c0002t0003g0175a0002c0003t0003g0191a0002c0003t0003g0192others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.3855+285C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55676203 | ||||||
chr14:55676292
|
T | C | 4 | a0001c0004t0003g0003a0001c0004t0003g0005a0001c0004t0003g0006others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3855+374T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55676292 | ||||||
chr14:55676364
|
T | G | 1 | a0001c0001t0001g0299 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3855+446T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55676364 | ||||||
chr14:55676414
|
G | A | 113 | a0001c0001t0001g0004a0001c0001t0002g0008a0001c0001t0002g0009others(110): Show | 113 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.3855+496G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55676414 | ||||||
chr14:55676559
|
G | A | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.3855+641G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55676559 | ||||||
chr14:55676654
|
A | G | 2 | a0001c0001t0001g0153a0013c0010t0001g0144 | 2 | HG01358.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.3855+736A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55676654 | ||||||
chr14:55676882
|
GA | G | 3 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0064 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3855+965delA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55676882 | ||||||
chr14:55676890
|
A | T | 1 | a0001c0001t0002g0027 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3855+972A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55676890 | ||||||
chr14:55676919
|
G | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3855+1001G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55676919 | ||||||
chr14:55676941
|
C | T | 1 | a0001c0001t0003g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3855+1023C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55676941 | ||||||
chr14:55677029
|
C | T | 8 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0116others(5): Show | 8 | HG01123.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.3855+1111C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55677029 | ||||||
chr14:55677083
|
A | C | 4 | a0003c0016t0003g0190a0003c0019t0003g0189a0006c0008t0003g0187others(1): Show | 4 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3855+1165A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55677083 | ||||||
chr14:55677209
|
C | T | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.3856-1143C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55677209 | ||||||
chr14:55677214
|
G | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.3856-1138G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55677214 | ||||||
chr14:55677250
|
C | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.3856-1102C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55677250 | ||||||
chr14:55677380
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3856-972G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55677380 | ||||||
chr14:55677401
|
C | T | 1 | a0001c0001t0002g0042 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3856-951C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55677401 | ||||||
chr14:55677425
|
C | T | 4 | a0001c0001t0001g0243a0001c0004t0003g0003a0001c0004t0003g0005others(1): Show | 4 | HG02723.hp1 HG03041.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3856-927C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55677425 | ||||||
chr14:55677473
|
T | TA | 17 | a0001c0001t0001g0126a0001c0001t0001g0215a0001c0001t0001g0228others(14): Show | 17 | HG01243.hp2 HG02145.hp1 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.3856-857dupA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | INFO_REALIGN_3_PRIME | chr14 | 55677473 | |||||
chr14:55677473
|
TAAAAAAA others(4): Show |
T | 84 | a0001c0001t0001g0142a0001c0001t0001g0239a0001c0001t0001g0240others(81): Show | 84 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.3856-867_3856-857d others(13): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | INFO_REALIGN_3_PRIME | chr14 | 55677473 | |||||
chr14:55677474
|
A | G | 22 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0099others(19): Show | 22 | HG01074.hp1 HG01081.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.3856-878A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55677474 | ||||||
chr14:55677475
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3856-877A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55677475 | ||||||
chr14:55677919
|
A | G | 7 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.3856-433A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55677919 | ||||||
chr14:55677989
|
C | T | 1 | a0010c0011t0005g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3856-363C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55677989 | ||||||
chr14:55678300
|
A | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.3856-52A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55678300 | ||||||
chr14:55678330
|
T | C | 1 | a0001c0001t0002g0028 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3856-22T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 41/43 | chr14 | 55678330 | ||||||
chr14:55678525
|
C | T | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3948+81C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 42/43 | chr14 | 55678525 | ||||||
chr14:55678552
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3948+108T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 42/43 | chr14 | 55678552 | ||||||
chr14:55678594
|
A | G | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.3948+150A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 42/43 | chr14 | 55678594 | ||||||
chr14:55678649
|
G | A | 1 | a0001c0001t0002g0071 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3948+205G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 42/43 | chr14 | 55678649 | ||||||
chr14:55678660
|
A | G | 1 | a0001c0004t0003g0003 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3948+216A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 42/43 | chr14 | 55678660 | ||||||
chr14:55678889
|
C | T | 7 | a0001c0001t0001g0224a0001c0001t0001g0233a0001c0001t0002g0010others(4): Show | 7 | HG02165.hp2 HG04228.hp2 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.3948+445C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 42/43 | chr14 | 55678889 | ||||||
chr14:55678950
|
G | C | 1 | a0001c0001t0001g0004 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3948+506G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 42/43 | chr14 | 55678950 | ||||||
chr14:55679256
|
G | A | 1 | a0001c0009t0001g0084 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3949-309G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 42/43 | chr14 | 55679256 | ||||||
chr14:55679269
|
T | C | 90 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0107others(87): Show | 90 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.3949-296T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 42/43 | chr14 | 55679269 | ||||||
chr14:55679271
|
T | C | 88 | a0001c0001t0001g0099a0001c0001t0001g0107a0001c0001t0001g0108others(85): Show | 88 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.3949-294T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 42/43 | chr14 | 55679271 | ||||||
chr14:55679510
|
T | G | 120 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0107others(117): Show | 120 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.3949-55T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 42/43 | chr14 | 55679510 | ||||||
chr14:55679937
|
G | A | 1 | a0001c0001t0002g0041 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.4069+252G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55679937 | ||||||
chr14:55679976
|
G | T | 22 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.4069+291G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55679976 | ||||||
chr14:55680193
|
C | T | 1 | a0010c0011t0005g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4069+508C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55680193 | ||||||
chr14:55680228
|
G | A | 2 | a0001c0001t0002g0012a0001c0001t0002g0020 | 2 | HG00558.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.4069+543G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55680228 | ||||||
chr14:55680369
|
GT | G | 25 | a0001c0001t0001g0217a0001c0002t0003g0175a0001c0002t0003g0176others(22): Show | 25 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.4069+699delT | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | INFO_REALIGN_3_PRIME | chr14 | 55680369 | |||||
chr14:55680370
|
T | G | 7 | a0001c0001t0001g0087a0001c0001t0001g0095a0001c0001t0001g0097others(4): Show | 7 | HG02970.hp1 HG03195.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.4069+685T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55680370 | ||||||
chr14:55680558
|
T | C | 9 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.4069+873T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55680558 | ||||||
chr14:55680621
|
G | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0243others(1): Show | 4 | HG02886.hp2 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.4069+936G>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55680621 | ||||||
chr14:55680822
|
G | T | 100 | a0001c0001t0001g0004a0001c0001t0001g0239a0001c0001t0001g0240others(97): Show | 100 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.4069+1137G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55680822 | ||||||
chr14:55680978
|
G | A | 88 | a0001c0001t0001g0004a0001c0001t0001g0239a0001c0001t0001g0240others(85): Show | 88 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.4069+1293G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55680978 | ||||||
chr14:55681040
|
A | G | 2 | a0003c0016t0003g0190a0003c0019t0003g0189 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.4069+1355A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55681040 | ||||||
chr14:55681370
|
G | T | 1 | a0009c0014t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4069+1685G>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55681370 | ||||||
chr14:55681387
|
C | G | 89 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0239others(86): Show | 89 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.4069+1702C>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55681387 | ||||||
chr14:55681525
|
T | G | 2 | a0004c0007t0002g0013a0004c0007t0002g0287 | 2 | HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.4069+1840T>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55681525 | ||||||
chr14:55681539
|
T | C | 88 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0107others(85): Show | 88 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.4069+1854T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55681539 | ||||||
chr14:55681548
|
T | C | 1 | a0008c0012t0002g0060 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.4069+1863T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55681548 | ||||||
chr14:55681608
|
G | A | 1 | a0009c0014t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4069+1923G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55681608 | ||||||
chr14:55681631
|
C | T | 4 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 4 | NA18941.hp1 NA18950.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.4069+1946C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55681631 | ||||||
chr14:55681723
|
G | A | 1 | a0001c0001t0002g0025 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.4069+2038G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55681723 | ||||||
chr14:55681754
|
A | G | 4 | a0003c0016t0003g0190a0003c0019t0003g0189a0006c0008t0003g0187others(1): Show | 4 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4069+2069A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55681754 | ||||||
chr14:55681857
|
C | T | 1 | a0003c0019t0003g0189 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4069+2172C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55681857 | ||||||
chr14:55681952
|
G | A | 1 | a0010c0011t0005g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4070-2147G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55681952 | ||||||
chr14:55681962
|
C | A | 99 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0002g0008others(96): Show | 99 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.4070-2137C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55681962 | ||||||
chr14:55681998
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4070-2101G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55681998 | ||||||
chr14:55682198
|
A | G | 8 | a0001c0009t0001g0084a0001c0009t0001g0086a0003c0016t0003g0190others(5): Show | 8 | HG00639.hp2 HG02559.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.4070-1901A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55682198 | ||||||
chr14:55682491
|
TTACCTTA others(29): Show |
T | 1 | a0012c0013t0001g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4070-1607_4070-157 others(40): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55682491 | ||||||
chr14:55682633
|
T | C | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.4070-1466T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55682633 | ||||||
chr14:55682758
|
G | A | 1 | a0002c0003t0003g0194 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4070-1341G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55682758 | ||||||
chr14:55682868
|
T | A | 81 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0011others(78): Show | 81 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.4070-1231T>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55682868 | ||||||
chr14:55682958
|
C | T | 1 | a0001c0002t0003g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4070-1141C>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55682958 | ||||||
chr14:55683118
|
C | A | 1 | a0001c0001t0001g0305 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4070-981C>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55683118 | ||||||
chr14:55683237
|
A | G | 1 | a0009c0014t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4070-862A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55683237 | ||||||
chr14:55683379
|
A | G | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.4070-720A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55683379 | ||||||
chr14:55683392
|
T | C | 3 | a0001c0001t0001g0118a0001c0001t0001g0138a0001c0001t0001g0146 | 3 | NA18970.hp1 NA19056.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.4070-707T>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55683392 | ||||||
chr14:55683408
|
A | G | 5 | a0002c0003t0003g0191a0002c0003t0003g0192a0002c0003t0003g0193others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.4070-691A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55683408 | ||||||
chr14:55683433
|
A | G | 205 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0088others(202): Show | 205 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.4070-666A>G | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55683433 | ||||||
chr14:55683519
|
A | C | 1 | a0001c0001t0002g0288 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4070-580A>C | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55683519 | ||||||
chr14:55683527
|
A | T | 1 | a0001c0002t0003g0181 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4070-572A>T | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55683527 | ||||||
chr14:55683636
|
GTCTC | G | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.4070-459_4070-456d others(6): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | INFO_REALIGN_3_PRIME | chr14 | 55683636 | |||||
chr14:55683671
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4070-428G>A | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | chr14 | 55683671 | ||||||
chr14:55683706
|
TA | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0087others(179): Show | 184 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.4070-376delA | KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | INFO_REALIGN_3_PRIME | chr14 | 55683706 | |||||
chr14:55683706
|
TAA | T | 96 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0101others(93): Show | 96 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.4070-377_4070-376d others(4): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | INFO_REALIGN_3_PRIME | chr14 | 55683706 | |||||
chr14:55683706
|
TAAA | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0163a0001c0001t0001g0243others(5): Show | 8 | HG02055.hp2 HG02071.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.4070-378_4070-376d others(5): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | INFO_REALIGN_3_PRIME | chr14 | 55683706 | |||||
chr14:55683706
|
TAAAA | T | 12 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0178others(9): Show | 12 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.4070-379_4070-376d others(6): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 43/43 | INFO_REALIGN_3_PRIME | chr14 | 55683706 |