geneid | 23247 |
---|---|
ensemblid | ENSG00000047578.14 |
hgncid | 29068 |
symbol | KATNIP |
name | katanin interacting protein |
refseq_nuc | NM_015202.5 |
refseq_prot | NP_056017.4 |
ensembl_nuc | ENST00000261588.10 |
ensembl_prot | ENSP00000261588.4 |
mane_status | MANE Select |
chr | chr16 |
start | 27550144 |
end | 27780344 |
strand | + |
ver | v1.2 |
region | chr16:27550144-27780344 |
region5000 | chr16:27545144-27785344 |
regionname0 | KATNIP_chr16_27550144_27780344 |
regionname5000 | KATNIP_chr16_27545144_27785344 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1618 | 87 | 53 | 9 | 21 | 3 | 1 | 12 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0002 | 0/0 | 1618 | 17 | 4 | 0 | 13 | 0 | 0 | 7 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0003 | 0/0 | 1618 | 13 | 1 | 6 | 0 | 4 | 2 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0004 | 0/0 | 1618 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0005 | 0/0 | 1618 | 5 | 0 | 1 | 4 | 0 | 0 | 3 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0006 | 0/0 | 1618 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0007 | 0/0 | 1618 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0008 | 0/0 | 1618 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0009 | 0/0 | 1618 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0010 | 0/0 | 1618 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0011 | 0/0 | 1618 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0012 | 0/0 | 1618 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0013 | 0/0 | 1618 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0014 | 0/0 | 1618 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0015 | 0/0 | 1618 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0016 | 1/0 | 1618 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0017 | 0/1 | 1618 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0018 | 0/0 | 1618 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0019 | 0/0 | 1618 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 4857 | 57 | 28 | 6 | 20 | 2 | 1 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0002 | 0/0 | 4857 | 16 | 3 | 0 | 13 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0003 | 0/0 | 4857 | 13 | 1 | 6 | 0 | 4 | 2 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0004 | 0/0 | 4857 | 9 | 7 | 1 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0005 | 0/0 | 4857 | 6 | 6 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0006 | 0/0 | 4857 | 5 | 0 | 1 | 4 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0007 | 0/0 | 4857 | 5 | 5 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0008 | 0/0 | 4857 | 4 | 4 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0009 | 0/0 | 4857 | 3 | 0 | 2 | 0 | 0 | 1 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0010 | 0/0 | 4857 | 3 | 3 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0011 | 0/0 | 4857 | 2 | 1 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0012 | 0/0 | 4857 | 2 | 2 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0013 | 0/0 | 4857 | 2 | 0 | 0 | 2 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0014 | 0/0 | 4857 | 2 | 0 | 2 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0015 | 0/0 | 4857 | 2 | 2 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0016 | 0/0 | 4857 | 2 | 2 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0017 | 0/0 | 4857 | 2 | 2 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0018 | 0/0 | 4857 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0019 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0020 | 0/0 | 4857 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0021 | 0/1 | 4857 | 1 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0022 | 1/0 | 4857 | 1 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0023 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0024 | 0/0 | 4857 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0025 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0026 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0027 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0028 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0029 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0030 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0031 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0032 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0033 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
c0034 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
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 | 1743 | 67 | 24 | 13 | 23 | 3 | 2 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
t0002 | 0/0 | 1743 | 36 | 24 | 6 | 0 | 4 | 2 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
t0003 | 0/0 | 1741 | 22 | 7 | 0 | 15 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
t0004 | 0/0 | 1743 | 16 | 15 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
t0005 | 0/0 | 1736 | 4 | 4 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
t0006 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
t0007 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
t0008 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
t0009 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
t0010 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
t0011 | 0/0 | 1743 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
t0012 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0016 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4857 | 57 | 28 | 6 | 20 | 2 | 1 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0004 | 0/0 | 4857 | 9 | 7 | 1 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0005 | 0/0 | 4857 | 6 | 6 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0008 | 0/0 | 4857 | 4 | 4 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0011 | 0/0 | 4857 | 2 | 1 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0012 | 0/0 | 4857 | 2 | 2 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0015 | 0/0 | 4857 | 2 | 2 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0018 | 0/0 | 4857 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0023 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0024 | 0/0 | 4857 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0026 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0028 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0002c0002 | 0/0 | 4857 | 16 | 3 | 0 | 13 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0002c0029 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0003c0003 | 0/0 | 4857 | 13 | 1 | 6 | 0 | 4 | 2 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0004c0007 | 0/0 | 4857 | 5 | 5 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0004c0030 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0004c0034 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0005c0006 | 0/0 | 4857 | 5 | 0 | 1 | 4 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0006c0009 | 0/0 | 4857 | 3 | 0 | 2 | 0 | 0 | 1 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0007c0010 | 0/0 | 4857 | 3 | 3 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0008c0016 | 0/0 | 4857 | 2 | 2 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0008c0031 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0009c0014 | 0/0 | 4857 | 2 | 0 | 2 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0010c0013 | 0/0 | 4857 | 2 | 0 | 0 | 2 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0011c0017 | 0/0 | 4857 | 2 | 2 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0012c0033 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0013c0027 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0014c0019 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0015c0020 | 0/0 | 4857 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0016c0022 | 1/0 | 4857 | 1 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0017c0021 | 0/1 | 4857 | 1 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0018c0025 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0019c0032 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6599 | 34 | 7 | 6 | 18 | 2 | 1 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0001t0002 | 0/0 | 6599 | 10 | 10 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0001t0004 | 0/0 | 6599 | 9 | 9 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0001t0006 | 0/0 | 6599 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0001t0007 | 0/0 | 6599 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0001t0008 | 0/0 | 6599 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0001t0009 | 0/0 | 6599 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0004t0001 | 0/0 | 6599 | 6 | 4 | 1 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0004t0002 | 0/0 | 6599 | 3 | 3 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0005t0001 | 0/0 | 6599 | 3 | 3 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0005t0002 | 0/0 | 6599 | 3 | 3 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0008t0004 | 0/0 | 6599 | 4 | 4 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0011t0002 | 0/0 | 6599 | 2 | 1 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0012t0002 | 0/0 | 6599 | 2 | 2 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0015t0001 | 0/0 | 6599 | 2 | 2 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0018t0011 | 0/0 | 6599 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0023t0001 | 0/0 | 6599 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0024t0001 | 0/0 | 6599 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0026t0004 | 0/0 | 6599 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0001c0028t0004 | 0/0 | 6599 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0002c0002t0003 | 0/0 | 6597 | 16 | 3 | 0 | 13 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0002c0029t0003 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0003c0003t0001 | 0/0 | 6599 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0003c0003t0002 | 0/0 | 6599 | 12 | 1 | 5 | 0 | 4 | 2 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0004c0007t0001 | 0/0 | 6599 | 3 | 3 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0004c0007t0010 | 0/0 | 6599 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0004c0007t0012 | 0/0 | 6599 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0004c0030t0005 | 0/0 | 6592 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0004c0034t0005 | 0/0 | 6592 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0005c0006t0001 | 0/0 | 6599 | 5 | 0 | 1 | 4 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0006c0009t0001 | 0/0 | 6599 | 3 | 0 | 2 | 0 | 0 | 1 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0007c0010t0002 | 0/0 | 6599 | 3 | 3 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0008c0016t0001 | 0/0 | 6599 | 2 | 2 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0008c0031t0001 | 0/0 | 6599 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0009c0014t0001 | 0/0 | 6599 | 2 | 0 | 2 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0010c0013t0003 | 0/0 | 6597 | 2 | 0 | 0 | 2 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0011c0017t0005 | 0/0 | 6592 | 2 | 2 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0012c0033t0002 | 0/0 | 6599 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0013c0027t0001 | 0/0 | 6599 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0014c0019t0003 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0015c0020t0004 | 0/0 | 6599 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0016c0022t0001 | 1/0 | 6599 | 1 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0017c0021t0001 | 0/1 | 6599 | 1 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0018c0025t0003 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
a0019c0032t0003 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | copy fasta | chr16 | 27545144 | 27785344 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0001t0009g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0004t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0004t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0004t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0004t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0004t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0004t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0005t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0005t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0005t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0005t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0005t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0005t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0008t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0008t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0008t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0008t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0011t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0011t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0012t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0012t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0015t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0015t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0018t0011g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0023t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0024t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0026t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0001c0028t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0002c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0002c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0002c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0002c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0002c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0002c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0002c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0002c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0002c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0002c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0002c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0002c0002t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0002c0002t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0002c0002t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0002c0029t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0003c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0003c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0003c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0003c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0003c0003t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0003c0003t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0003c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0003c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0003c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0003c0003t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0003c0003t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0003c0003t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0003c0003t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0004c0007t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0004c0007t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0004c0007t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0004c0007t0010g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0004c0007t0012g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0004c0030t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0004c0034t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0005c0006t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0005c0006t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0005c0006t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0005c0006t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0005c0006t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0006c0009t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0006c0009t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0006c0009t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0007c0010t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0007c0010t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0007c0010t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0008c0016t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0008c0016t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0008c0031t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0009c0014t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0009c0014t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0010c0013t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0010c0013t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0011c0017t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0011c0017t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0012c0033t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0013c0027t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0014c0019t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0015c0020t0004g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0016c0022t0001g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0017c0021t0001g0016 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0018c0025t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
a0019c0032t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0003 | t0002 | g0128 | EUR | GBR | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG00099 | hp2 | a0001 | c0004 | t0001 | g0042 | EUR | GBR | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG00140 | hp1 | a0003 | c0003 | t0002 | g0120 | EUR | GBR | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | GBR | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG00408 | hp1 | a0002 | c0002 | t0003 | g0065 | EAS | CHS | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG00741 | hp2 | a0005 | c0006 | t0001 | g0085 | AMR | PUR | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01106 | hp1 | a0001 | c0018 | t0011 | g0122 | AMR | PUR | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01109 | hp2 | a0001 | c0004 | t0001 | g0138 | AMR | PUR | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01243 | hp1 | a0009 | c0014 | t0001 | g0018 | AMR | PUR | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01243 | hp2 | a0001 | c0011 | t0002 | g0141 | AMR | PUR | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01258 | hp1 | a0009 | c0014 | t0001 | g0043 | AMR | CLM | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01258 | hp2 | a0003 | c0003 | t0002 | g0130 | AMR | CLM | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01261 | hp1 | a0006 | c0009 | t0001 | g0036 | AMR | CLM | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01261 | hp2 | a0003 | c0003 | t0001 | g0127 | AMR | CLM | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01358 | hp2 | a0003 | c0003 | t0002 | g0123 | AMR | CLM | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01361 | hp1 | a0003 | c0003 | t0002 | g0131 | AMR | CLM | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01361 | hp2 | a0006 | c0009 | t0001 | g0035 | AMR | CLM | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01515 | hp1 | a0003 | c0003 | t0002 | g0129 | EUR | IBS | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01515 | hp2 | a0015 | c0020 | t0004 | g0008 | EUR | IBS | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01517 | hp1 | a0003 | c0003 | t0002 | g0126 | EUR | IBS | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG01978 | hp2 | a0003 | c0003 | t0002 | g0140 | AMR | PEL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | ACB | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02055 | hp2 | a0008 | c0031 | t0001 | g0107 | AFR | ACB | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02056 | hp1 | a0005 | c0006 | t0001 | g0013 | EAS | KHV | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02074 | hp1 | a0002 | c0002 | t0003 | g0104 | EAS | KHV | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02132 | hp2 | a0002 | c0002 | t0003 | g0062 | EAS | KHV | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02135 | hp1 | a0002 | c0002 | t0003 | g0110 | EAS | KHV | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | ACB | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02145 | hp2 | a0011 | c0017 | t0005 | g0151 | AFR | ACB | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CDX | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CDX | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02165 | hp2 | a0002 | c0002 | t0003 | g0068 | EAS | CDX | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02273 | hp2 | a0003 | c0003 | t0002 | g0125 | AMR | PEL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | ACB | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02280 | hp2 | a0001 | c0028 | t0004 | g0109 | AFR | ACB | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02451 | hp1 | a0008 | c0016 | t0001 | g0076 | AFR | ACB | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0081 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02615 | hp2 | a0004 | c0007 | t0001 | g0075 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02622 | hp2 | a0002 | c0029 | t0003 | g0101 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02630 | hp1 | a0001 | c0012 | t0002 | g0137 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02647 | hp1 | a0001 | c0004 | t0002 | g0070 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02683 | hp1 | a0003 | c0003 | t0002 | g0121 | SAS | PJL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02717 | hp1 | a0012 | c0033 | t0002 | g0142 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0051 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02738 | hp1 | a0006 | c0009 | t0001 | g0096 | SAS | PJL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02738 | hp2 | a0003 | c0003 | t0002 | g0094 | SAS | PJL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02809 | hp2 | a0001 | c0004 | t0002 | g0073 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02818 | hp1 | a0001 | c0011 | t0002 | g0152 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02886 | hp1 | a0018 | c0025 | t0003 | g0111 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02886 | hp2 | a0004 | c0007 | t0001 | g0105 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02896 | hp1 | a0007 | c0010 | t0002 | g0112 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02896 | hp2 | a0001 | c0004 | t0002 | g0069 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02897 | hp1 | a0001 | c0023 | t0001 | g0060 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02897 | hp2 | a0007 | c0010 | t0002 | g0113 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02922 | hp2 | a0001 | c0004 | t0001 | g0118 | AFR | ESN | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02965 | hp1 | a0001 | c0008 | t0004 | g0079 | AFR | ESN | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02965 | hp2 | a0002 | c0002 | t0003 | g0136 | AFR | ESN | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02970 | hp1 | a0001 | c0005 | t0001 | g0145 | AFR | ESN | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02970 | hp2 | a0001 | c0001 | t0008 | g0050 | AFR | ESN | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02976 | hp1 | a0001 | c0008 | t0004 | g0080 | AFR | ESN | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03041 | hp1 | a0001 | c0008 | t0004 | g0041 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03041 | hp2 | a0004 | c0030 | t0005 | g0115 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03098 | hp1 | a0001 | c0005 | t0002 | g0149 | AFR | MSL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | ESN | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03130 | hp2 | a0001 | c0004 | t0001 | g0116 | AFR | ESN | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03139 | hp1 | a0001 | c0012 | t0002 | g0143 | AFR | ESN | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03139 | hp2 | a0001 | c0005 | t0002 | g0147 | AFR | ESN | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03195 | hp1 | a0011 | c0017 | t0005 | g0150 | AFR | ESN | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03209 | hp1 | a0013 | c0027 | t0001 | g0004 | AFR | MSL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03209 | hp2 | a0004 | c0007 | t0010 | g0108 | AFR | MSL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03225 | hp1 | a0004 | c0034 | t0005 | g0119 | AFR | MSL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03225 | hp2 | a0001 | c0015 | t0001 | g0084 | AFR | MSL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03453 | hp1 | a0007 | c0010 | t0002 | g0114 | AFR | MSL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03453 | hp2 | a0002 | c0002 | t0003 | g0135 | AFR | MSL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03516 | hp2 | a0008 | c0016 | t0001 | g0077 | AFR | ESN | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03540 | hp1 | a0004 | c0007 | t0012 | g0106 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHB | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18747 | hp2 | a0002 | c0002 | t0003 | g0066 | EAS | CHB | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18906 | hp1 | a0001 | c0008 | t0004 | g0026 | AFR | YRI | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18906 | hp2 | a0001 | c0004 | t0001 | g0117 | AFR | YRI | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18950 | hp1 | a0002 | c0002 | t0003 | g0067 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18954 | hp1 | a0002 | c0002 | t0003 | g0063 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18959 | hp2 | a0002 | c0002 | t0003 | g0098 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18962 | hp1 | a0002 | c0002 | t0003 | g0072 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18971 | hp1 | a0002 | c0002 | t0003 | g0099 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18971 | hp2 | a0005 | c0006 | t0001 | g0058 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18986 | hp2 | a0001 | c0024 | t0001 | g0078 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18995 | hp1 | a0001 | c0001 | t0007 | g0091 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA18995 | hp2 | a0002 | c0002 | t0003 | g0102 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA19000 | hp1 | a0010 | c0013 | t0003 | g0103 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA19043 | hp1 | a0001 | c0004 | t0001 | g0132 | AFR | LWK | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA19043 | hp2 | a0001 | c0015 | t0001 | g0012 | AFR | LWK | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA19080 | hp1 | a0005 | c0006 | t0001 | g0064 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA19080 | hp2 | a0002 | c0002 | t0003 | g0097 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA19081 | hp2 | a0005 | c0006 | t0001 | g0059 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA19084 | hp1 | a0010 | c0013 | t0003 | g0061 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA19084 | hp2 | a0001 | c0001 | t0009 | g0055 | EAS | JPT | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA19240 | hp2 | a0001 | c0005 | t0001 | g0144 | AFR | YRI | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA20129 | hp1 | a0004 | c0007 | t0001 | g0074 | AFR | ASW | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ASW | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0037 | AFR | ACB | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02109 | hp2 | a0014 | c0019 | t0003 | g0100 | AFR | ACB | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02486 | hp1 | a0019 | c0032 | t0003 | g0001 | AFR | ACB | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03471 | hp1 | a0001 | c0005 | t0001 | g0146 | AFR | MSL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
HG03471 | hp2 | a0002 | c0002 | t0003 | g0134 | AFR | MSL | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | USA | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA20300 | hp2 | a0001 | c0005 | t0002 | g0148 | AFR | USA | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA21309 | hp1 | a0001 | c0026 | t0004 | g0032 | AFR | LWK | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
NA21309 | hp2 | a0003 | c0003 | t0002 | g0139 | AFR | LWK | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
homoSapiens_chm13v2 | hp1 | a0017 | c0021 | t0001 | g0016 | REF | REF | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
homoSapiens_grch38 | hp1 | a0016 | c0022 | t0001 | g0124 | REF | REF | KATNIP_chr16_27545144_27785344 | KATNIP | chr16 | 27545144 | 27785344 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:27628729
|
C | G | 1 | a0012 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.209C>G | p.Ser70Cys | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 4/28 | 236/6599 | 209/4857 | 70/1618 | chr16 | 27628729 | ||
chr16:27648710
|
A | G | 4 | a0004a0008a0011others(1): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
missense_variant | MODERATE | c.515A>G | p.Asn172Ser | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/28 | 542/6599 | 515/4857 | 172/1618 | chr16 | 27648710 | ||
chr16:27677816
|
G | T | 1 | a0007 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.628G>T | p.Asp210Tyr | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/28 | 655/6599 | 628/4857 | 210/1618 | chr16 | 27677816 | ||
chr16:27708880
|
C | T | 1 | a0003 | 13 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(10): Show |
missense_variant | MODERATE | c.1565C>T | p.Thr522Met | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/28 | 1592/6599 | 1565/4857 | 522/1618 | chr16 | 27708880 | ||
chr16:27740318
|
A | C | 1 | a0011 | 2 | HG02145.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.2021A>C | p.Gln674Pro | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/28 | 2048/6599 | 2021/4857 | 674/1618 | chr16 | 27740318 | ||
chr16:27740477
|
A | T | 1 | a0019 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.2180A>T | p.His727Leu | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/28 | 2207/6599 | 2180/4857 | 727/1618 | chr16 | 27740477 | ||
chr16:27740549
|
C | T | 1 | a0013 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.2252C>T | p.Thr751Ile | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/28 | 2279/6599 | 2252/4857 | 751/1618 | chr16 | 27740549 | ||
chr16:27740663
|
C | T | 1 | a0014 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.2366C>T | p.Pro789Leu | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/28 | 2393/6599 | 2366/4857 | 789/1618 | chr16 | 27740663 | ||
chr16:27749614
|
G | A | 1 | a0015 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.2654G>A | p.Arg885Gln | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/28 | 2681/6599 | 2654/4857 | 885/1618 | chr16 | 27749614 | ||
chr16:27749719
|
C | T | 2 | a0005a0009 | 7 | HG00741.hp2 HG01243.hp1 HG01258.hp1 others(4): Show |
missense_variant | MODERATE | c.2759C>T | p.Pro920Leu | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/28 | 2786/6599 | 2759/4857 | 920/1618 | chr16 | 27749719 | ||
chr16:27751922
|
C | T | 1 | a0018 | 1 | HG02886.hp1 | missense_variant&splice_region_variant | MODERATE | c.3550C>T | p.Arg1184Trp | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/28 | 3577/6599 | 3550/4857 | 1184/1618 | chr16 | 27751922 | ||
chr16:27761433
|
G | A | 1 | a0014 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.3652G>A | p.Ala1218Thr | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/28 | 3679/6599 | 3652/4857 | 1218/1618 | chr16 | 27761433 | ||
chr16:27761500
|
C | T | 1 | a0009 | 2 | HG01243.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.3719C>T | p.Ala1240Val | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/28 | 3746/6599 | 3719/4857 | 1240/1618 | chr16 | 27761500 | ||
chr16:27761580
|
G | A | 18 | a0001a0002a0003others(15): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
missense_variant | MODERATE | c.3799G>A | p.Ala1267Thr | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/28 | 3826/6599 | 3799/4857 | 1267/1618 | chr16 | 27761580 | ||
chr16:27769911
|
G | C | 1 | a0008 | 3 | HG02055.hp2 HG02451.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.4026G>C | p.Glu1342Asp | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 21/28 | 4053/6599 | 4026/4857 | 1342/1618 | chr16 | 27769911 | ||
chr16:27769988
|
G | A | 1 | a0006 | 3 | HG01261.hp1 HG01361.hp2 HG02738.hp1 |
missense_variant | MODERATE | c.4103G>A | p.Arg1368Gln | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 21/28 | 4130/6599 | 4103/4857 | 1368/1618 | chr16 | 27769988 | ||
chr16:27773176
|
G | A | 1 | a0017 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.4276G>A | p.Glu1426Lys | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 23/28 | 4303/6599 | 4276/4857 | 1426/1618 | chr16 | 27773176 | ||
chr16:27774992
|
G | A | 1 | a0010 | 2 | NA19000.hp1 NA19084.hp1 |
missense_variant | MODERATE | c.4357G>A | p.Gly1453Arg | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/28 | 4384/6599 | 4357/4857 | 1453/1618 | chr16 | 27774992 | ||
chr16:27777957
|
G | A | 3 | a0002a0010a0019 | 20 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(17): Show |
missense_variant | MODERATE | c.4789G>A | p.Val1597Ile | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 27/28 | 4816/6599 | 4789/4857 | 1597/1618 | chr16 | 27777957 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:27550176
|
C | T | 1 | a0004c0034 | 1 | HG03225.hp1 | splice_region_variant&synonymous_variant | LOW | c.6C>T | p.Asp2Asp | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/28 | 33/6599 | 6/4857 | 2/1618 | chr16 | 27550176 | ||
chr16:27573920
|
C | G | 2 | a0004c0034a0011c0017 | 3 | HG02145.hp2 HG03195.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.27C>G | p.Ala9Ala | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/28 | 54/6599 | 27/4857 | 9/1618 | chr16 | 27573920 | ||
chr16:27628766
|
A | G | 7 | a0004c0007a0004c0030a0004c0034others(4): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
synonymous_variant | LOW | c.246A>G | p.Ser82Ser | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 4/28 | 273/6599 | 246/4857 | 82/1618 | chr16 | 27628766 | ||
chr16:27681514
|
G | A | 6 | a0001c0005a0001c0011a0001c0018others(3): Show | 26 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(23): Show |
synonymous_variant | LOW | c.924G>A | p.Gln308Gln | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/28 | 951/6599 | 924/4857 | 308/1618 | chr16 | 27681514 | ||
chr16:27698476
|
C | T | 1 | a0001c0018 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.1089C>T | p.Ala363Ala | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 9/28 | 1116/6599 | 1089/4857 | 363/1618 | chr16 | 27698476 | ||
chr16:27698485
|
A | G | 1 | a0002c0029 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1098A>G | p.Pro366Pro | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 9/28 | 1125/6599 | 1098/4857 | 366/1618 | chr16 | 27698485 | ||
chr16:27698491
|
C | T | 1 | a0001c0028 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.1104C>T | p.Ser368Ser | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 9/28 | 1131/6599 | 1104/4857 | 368/1618 | chr16 | 27698491 | ||
chr16:27708722
|
G | A | 2 | a0001c0012a0014c0019 | 3 | HG02109.hp2 HG02630.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.1407G>A | p.Arg469Arg | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/28 | 1434/6599 | 1407/4857 | 469/1618 | chr16 | 27708722 | ||
chr16:27740427
|
C | T | 1 | a0001c0015 | 2 | HG03225.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.2130C>T | p.Asp710Asp | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/28 | 2157/6599 | 2130/4857 | 710/1618 | chr16 | 27740427 | ||
chr16:27740472
|
T | C | 1 | a0001c0018 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.2175T>C | p.Pro725Pro | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/28 | 2202/6599 | 2175/4857 | 725/1618 | chr16 | 27740472 | ||
chr16:27740679
|
C | T | 1 | a0001c0026 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.2382C>T | p.Ile794Ile | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/28 | 2409/6599 | 2382/4857 | 794/1618 | chr16 | 27740679 | ||
chr16:27740814
|
C | T | 10 | a0001c0005a0001c0011a0001c0018others(7): Show | 35 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(32): Show |
synonymous_variant | LOW | c.2517C>T | p.Asp839Asp | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/28 | 2544/6599 | 2517/4857 | 839/1618 | chr16 | 27740814 | ||
chr16:27749678
|
C | T | 1 | a0004c0034 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.2718C>T | p.Phe906Phe | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/28 | 2745/6599 | 2718/4857 | 906/1618 | chr16 | 27749678 | ||
chr16:27749876
|
T | C | 1 | a0008c0031 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.2916T>C | p.Pro972Pro | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/28 | 2943/6599 | 2916/4857 | 972/1618 | chr16 | 27749876 | ||
chr16:27749888
|
C | T | 1 | a0018c0025 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.2928C>T | p.Arg976Arg | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/28 | 2955/6599 | 2928/4857 | 976/1618 | chr16 | 27749888 | ||
chr16:27749975
|
G | A | 2 | a0001c0012a0014c0019 | 3 | HG02109.hp2 HG02630.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.3015G>A | p.Pro1005Pro | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/28 | 3042/6599 | 3015/4857 | 1005/1618 | chr16 | 27749975 | ||
chr16:27750065
|
C | T | 1 | a0001c0024 | 1 | NA18986.hp2 | synonymous_variant | LOW | c.3105C>T | p.Ile1035Ile | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/28 | 3132/6599 | 3105/4857 | 1035/1618 | chr16 | 27750065 | ||
chr16:27750224
|
C | T | 3 | a0004c0030a0004c0034a0011c0017 | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
synonymous_variant | LOW | c.3264C>T | p.Gly1088Gly | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/28 | 3291/6599 | 3264/4857 | 1088/1618 | chr16 | 27750224 | ||
chr16:27751789
|
T | C | 14 | a0001c0004a0001c0005a0001c0012others(11): Show | 47 | HG00099.hp2 HG00408.hp1 HG01109.hp2 others(44): Show |
synonymous_variant | LOW | c.3417T>C | p.Ser1139Ser | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/28 | 3444/6599 | 3417/4857 | 1139/1618 | chr16 | 27751789 | ||
chr16:27751864
|
G | A | 1 | a0018c0025 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.3492G>A | p.Thr1164Thr | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/28 | 3519/6599 | 3492/4857 | 1164/1618 | chr16 | 27751864 | ||
chr16:27754181
|
G | A | 1 | a0001c0008 | 4 | HG02965.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
synonymous_variant | LOW | c.3561G>A | p.Glu1187Glu | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/28 | 3588/6599 | 3561/4857 | 1187/1618 | chr16 | 27754181 | ||
chr16:27761570
|
C | T | 3 | a0001c0011a0001c0023a0012c0033 | 4 | HG01243.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
synonymous_variant | LOW | c.3789C>T | p.Asp1263Asp | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/28 | 3816/6599 | 3789/4857 | 1263/1618 | chr16 | 27761570 | ||
chr16:27774991
|
C | T | 2 | a0001c0011a0012c0033 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
synonymous_variant | LOW | c.4356C>T | p.Gly1452Gly | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/28 | 4383/6599 | 4356/4857 | 1452/1618 | chr16 | 27774991 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:27778657
|
C | A | 3 | a0004c0030t0005a0004c0034t0005a0011c0017t0005 | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*28C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 28/28 | 28 | chr16 | 27778657 | |||||
chr16:27778955
|
G | A | 6 | a0001c0001t0004a0001c0001t0006a0001c0008t0004others(3): Show | 17 | HG01515.hp2 HG02055.hp1 HG02109.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*326G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 28/28 | 326 | chr16 | 27778955 | |||||
chr16:27779128
|
G | A | 1 | a0001c0001t0007 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*499G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 28/28 | 499 | chr16 | 27779128 | |||||
chr16:27779271
|
CTG | C | 9 | a0002c0002t0003a0002c0029t0003a0004c0030t0005others(6): Show | 26 | HG00408.hp1 HG02074.hp1 HG02109.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*647_*648delTG | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 28/28 | 647 | INFO_REALIGN_3_PRIME | chr16 | 27779271 | ||||
chr16:27779479
|
G | C | 1 | a0001c0001t0008 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*850G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 28/28 | 850 | chr16 | 27779479 | |||||
chr16:27779605
|
C | T | 1 | a0004c0007t0012 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*976C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 28/28 | 976 | chr16 | 27779605 | |||||
chr16:27779726
|
G | A | 1 | a0001c0001t0009 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1097G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 28/28 | 1097 | chr16 | 27779726 | |||||
chr16:27779902
|
C | G | 1 | a0001c0018t0011 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1273C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 28/28 | 1273 | chr16 | 27779902 | |||||
chr16:27780035
|
G | A | 1 | a0004c0007t0010 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1406G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 28/28 | 1406 | chr16 | 27780035 | |||||
chr16:27780145
|
G | C | 14 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(11): Show | 43 | HG00099.hp1 HG00140.hp1 HG01243.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1516G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 28/28 | 1516 | chr16 | 27780145 | |||||
chr16:27780260
|
ATGTAC | A | 3 | a0004c0030t0005a0004c0034t0005a0011c0017t0005 | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1635_*1639delACTG others(1): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 28/28 | 1635 | INFO_REALIGN_3_PRIME | chr16 | 27780260 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:27550263
|
G | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.7+86G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27550263 | ||||||
chr16:27550297
|
G | A | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.7+120G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27550297 | ||||||
chr16:27550339
|
C | G | 1 | a0002c0002t0003g0110 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.7+162C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27550339 | ||||||
chr16:27550406
|
C | T | 1 | a0001c0011t0002g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.7+229C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27550406 | ||||||
chr16:27550893
|
T | G | 1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.7+716T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27550893 | ||||||
chr16:27550954
|
G | T | 2 | a0011c0017t0005g0150a0011c0017t0005g0151 | 2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.7+777G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27550954 | ||||||
chr16:27551235
|
A | G | 6 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(3): Show | 6 | HG02970.hp1 HG03098.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+1058A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27551235 | ||||||
chr16:27551524
|
G | C | 1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.7+1347G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27551524 | ||||||
chr16:27551826
|
C | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+1649C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27551826 | ||||||
chr16:27551939
|
A | G | 1 | a0001c0012t0002g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.7+1762A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27551939 | ||||||
chr16:27552520
|
G | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG01358.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.7+2343G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27552520 | ||||||
chr16:27552686
|
G | GT | 38 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0086others(35): Show | 38 | HG00408.hp2 HG00741.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.7+2533dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27552686 | |||||
chr16:27552723
|
T | G | 1 | a0013c0027t0001g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.7+2546T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27552723 | ||||||
chr16:27552728
|
G | A | 1 | a0001c0001t0004g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.7+2551G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27552728 | ||||||
chr16:27552731
|
G | A | 1 | a0001c0001t0004g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.7+2554G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27552731 | ||||||
chr16:27552940
|
C | G | 2 | a0001c0008t0004g0079a0001c0008t0004g0080 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.7+2763C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27552940 | ||||||
chr16:27553014
|
T | G | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+2837T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27553014 | ||||||
chr16:27553147
|
C | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+2970C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27553147 | ||||||
chr16:27553552
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.7+3375C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27553552 | ||||||
chr16:27553553
|
G | A | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+3376G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27553553 | ||||||
chr16:27553917
|
G | A | 1 | a0001c0005t0001g0144 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7+3740G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27553917 | ||||||
chr16:27553976
|
G | C | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+3799G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27553976 | ||||||
chr16:27553981
|
A | AGAGAGGA others(30): Show |
1 | a0001c0001t0001g0006 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.7+3827_7+3863dupAG others(35): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27553981 | |||||
chr16:27554162
|
A | G | 1 | a0001c0024t0001g0078 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.7+3985A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27554162 | ||||||
chr16:27554299
|
C | T | 1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.7+4122C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27554299 | ||||||
chr16:27554418
|
T | C | 17 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(14): Show | 17 | HG01109.hp2 HG02145.hp2 HG02896.hp1 others(14): Show |
intron_variant | MODIFIER | c.7+4241T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27554418 | ||||||
chr16:27554427
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.7+4250T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27554427 | ||||||
chr16:27554638
|
G | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.7+4461G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27554638 | ||||||
chr16:27554642
|
G | T | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.7+4465G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27554642 | ||||||
chr16:27554737
|
G | T | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.7+4560G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27554737 | ||||||
chr16:27554780
|
T | C | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+4603T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27554780 | ||||||
chr16:27554789
|
C | CT | 5 | a0001c0011t0002g0141a0001c0011t0002g0152a0004c0034t0005g0119others(2): Show | 5 | HG01243.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+4634dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27554789 | |||||
chr16:27554789
|
CT | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(90): Show | 93 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.7+4634delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27554789 | |||||
chr16:27554842
|
G | A | 1 | a0015c0020t0004g0008 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.7+4665G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27554842 | ||||||
chr16:27554847
|
A | G | 2 | a0001c0028t0004g0109a0019c0032t0003g0001 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.7+4670A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27554847 | ||||||
chr16:27555082
|
G | A | 1 | a0003c0003t0002g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.7+4905G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27555082 | ||||||
chr16:27555375
|
G | C | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.7+5198G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27555375 | ||||||
chr16:27555792
|
C | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+5615C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27555792 | ||||||
chr16:27555831
|
C | T | 5 | a0001c0001t0001g0133a0001c0004t0001g0132a0002c0002t0003g0134others(2): Show | 5 | HG02258.hp1 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+5654C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27555831 | ||||||
chr16:27555856
|
A | G | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+5679A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27555856 | ||||||
chr16:27556028
|
T | C | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+5851T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27556028 | ||||||
chr16:27556084
|
A | G | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+5907A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27556084 | ||||||
chr16:27556126
|
CA | C | 9 | a0001c0001t0004g0051a0004c0007t0001g0074a0004c0007t0001g0075others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+5964delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27556126 | |||||
chr16:27556223
|
C | T | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.7+6046C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27556223 | ||||||
chr16:27556483
|
G | A | 1 | a0001c0001t0001g0009 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.7+6306G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27556483 | ||||||
chr16:27557060
|
T | C | 1 | a0001c0001t0001g0010 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.7+6883T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27557060 | ||||||
chr16:27557142
|
A | AT | 5 | a0002c0002t0003g0104a0008c0016t0001g0077a0010c0013t0003g0103others(2): Show | 5 | HG01515.hp2 HG02074.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+6982dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27557142 | |||||
chr16:27557323
|
G | A | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+7146G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27557323 | ||||||
chr16:27557430
|
AT | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.7+7272delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27557430 | |||||
chr16:27557430
|
ATT | A | 18 | a0001c0004t0002g0069a0001c0012t0002g0137a0001c0012t0002g0143others(15): Show | 18 | HG00408.hp1 HG02109.hp2 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.7+7271_7+7272delTT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27557430 | |||||
chr16:27557549
|
G | C | 1 | a0001c0001t0002g0011 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7+7372G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27557549 | ||||||
chr16:27557860
|
T | C | 1 | a0001c0015t0001g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.7+7683T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27557860 | ||||||
chr16:27557948
|
C | A | 1 | a0001c0001t0001g0009 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.7+7771C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27557948 | ||||||
chr16:27557996
|
C | T | 5 | a0001c0001t0001g0133a0001c0004t0001g0132a0002c0002t0003g0134others(2): Show | 5 | HG02258.hp1 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+7819C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27557996 | ||||||
chr16:27558829
|
T | TGATTGTG others(298): Show |
1 | a0001c0001t0004g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7+8667_7+8668insTT others(303): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27558829 | |||||
chr16:27558954
|
C | T | 7 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(4): Show | 7 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+8777C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27558954 | ||||||
chr16:27559033
|
T | C | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.7+8856T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27559033 | ||||||
chr16:27559063
|
C | T | 1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.7+8886C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27559063 | ||||||
chr16:27559128
|
G | A | 1 | a0003c0003t0002g0121 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.7+8951G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27559128 | ||||||
chr16:27559375
|
T | C | 1 | a0005c0006t0001g0013 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.7+9198T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27559375 | ||||||
chr16:27559383
|
C | G | 1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.7+9206C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27559383 | ||||||
chr16:27559427
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.7+9250G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27559427 | ||||||
chr16:27559473
|
G | C | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.7+9296G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27559473 | ||||||
chr16:27559537
|
A | G | 1 | a0001c0001t0002g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.7+9360A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27559537 | ||||||
chr16:27559680
|
C | CA | 9 | a0001c0018t0011g0122a0004c0007t0001g0074a0004c0007t0001g0075others(6): Show | 9 | HG01106.hp1 HG02055.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+9519dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27559680 | |||||
chr16:27559795
|
A | G | 1 | a0003c0003t0002g0121 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.7+9618A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27559795 | ||||||
chr16:27559817
|
G | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.7+9640G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27559817 | ||||||
chr16:27559866
|
A | G | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.7+9689A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27559866 | ||||||
chr16:27560080
|
A | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.7+9903A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27560080 | ||||||
chr16:27560117
|
A | G | 5 | a0001c0001t0001g0133a0001c0004t0001g0132a0002c0002t0003g0134others(2): Show | 5 | HG02258.hp1 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+9940A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27560117 | ||||||
chr16:27560236
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.7+10059C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27560236 | ||||||
chr16:27560238
|
C | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+10061C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27560238 | ||||||
chr16:27560283
|
G | GA | 15 | a0001c0001t0001g0015a0001c0001t0001g0082a0001c0001t0002g0014others(12): Show | 15 | HG01243.hp2 HG01978.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.7+10128dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27560283 | |||||
chr16:27560348
|
A | G | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+10171A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27560348 | ||||||
chr16:27560498
|
T | G | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+10321T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27560498 | ||||||
chr16:27560591
|
C | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+10414C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27560591 | ||||||
chr16:27560610
|
T | C | 2 | a0001c0028t0004g0109a0019c0032t0003g0001 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.7+10433T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27560610 | ||||||
chr16:27560895
|
G | A | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.7+10718G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27560895 | ||||||
chr16:27560995
|
T | A | 1 | a0001c0001t0002g0011 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7+10818T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27560995 | ||||||
chr16:27560997
|
C | G | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+10820C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27560997 | ||||||
chr16:27561097
|
C | T | 1 | a0001c0023t0001g0060 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.7+10920C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27561097 | ||||||
chr16:27561102
|
C | T | 1 | a0001c0001t0004g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.7+10925C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27561102 | ||||||
chr16:27561156
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7+10979C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27561156 | ||||||
chr16:27561186
|
AT | A | 11 | a0001c0001t0002g0071a0002c0029t0003g0101a0004c0007t0001g0074others(8): Show | 11 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.7+11024delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27561186 | |||||
chr16:27561201
|
T | C | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.7+11024T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27561201 | ||||||
chr16:27561225
|
A | G | 5 | a0001c0001t0001g0133a0001c0004t0001g0132a0002c0002t0003g0134others(2): Show | 5 | HG02258.hp1 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+11048A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27561225 | ||||||
chr16:27561346
|
C | T | 1 | a0001c0001t0004g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.7+11169C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27561346 | ||||||
chr16:27561922
|
G | A | 4 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+11745G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27561922 | ||||||
chr16:27562310
|
C | G | 1 | a0001c0001t0004g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.8-11591C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27562310 | ||||||
chr16:27562356
|
G | A | 16 | a0001c0024t0001g0078a0002c0002t0003g0062a0002c0002t0003g0063others(13): Show | 16 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.8-11545G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27562356 | ||||||
chr16:27562420
|
A | G | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8-11481A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27562420 | ||||||
chr16:27562938
|
C | T | 1 | a0010c0013t0003g0061 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.8-10963C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27562938 | ||||||
chr16:27563000
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | NA18747.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.8-10901C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27563000 | ||||||
chr16:27563036
|
A | G | 1 | a0001c0023t0001g0060 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.8-10865A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27563036 | ||||||
chr16:27563267
|
A | T | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.8-10634A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27563267 | ||||||
chr16:27563406
|
C | T | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.8-10495C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27563406 | ||||||
chr16:27563413
|
G | A | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-10488G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27563413 | ||||||
chr16:27563477
|
C | T | 3 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151 | 3 | HG02145.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.8-10424C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27563477 | ||||||
chr16:27563515
|
C | T | 3 | a0002c0002t0003g0097a0005c0006t0001g0058a0005c0006t0001g0059 | 3 | NA18971.hp2 NA19080.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.8-10386C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27563515 | ||||||
chr16:27563528
|
G | A | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.8-10373G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27563528 | ||||||
chr16:27563891
|
T | TA | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(81): Show | 84 | HG00408.hp2 HG00741.hp1 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.8-9984dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27563891 | |||||
chr16:27563891
|
T | TAA | 8 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0014others(5): Show | 8 | HG02572.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.8-9985_8-9984dupAA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27563891 | |||||
chr16:27563891
|
TAAAAAAA others(5): Show |
T | 2 | a0011c0017t0005g0150a0011c0017t0005g0151 | 2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.8-9995_8-9984delAA others(10): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27563891 | |||||
chr16:27564101
|
G | A | 2 | a0001c0001t0001g0047a0003c0003t0002g0094 | 2 | HG01109.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.8-9800G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27564101 | ||||||
chr16:27564352
|
C | T | 14 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(11): Show | 14 | HG01109.hp2 HG02896.hp1 HG02897.hp2 others(11): Show |
intron_variant | MODIFIER | c.8-9549C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27564352 | ||||||
chr16:27564670
|
A | G | 1 | a0004c0030t0005g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.8-9231A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27564670 | ||||||
chr16:27564742
|
G | A | 4 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-9159G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27564742 | ||||||
chr16:27564746
|
G | GGCTTGCT others(1): Show |
3 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151 | 3 | HG02145.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.8-9130_8-9123dupGC others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27564746 | |||||
chr16:27564945
|
G | T | 2 | a0001c0012t0002g0137a0001c0012t0002g0143 | 2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.8-8956G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27564945 | ||||||
chr16:27565149
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.8-8752C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27565149 | ||||||
chr16:27565720
|
A | C | 1 | a0001c0001t0004g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.8-8181A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27565720 | ||||||
chr16:27565788
|
A | C | 5 | a0001c0001t0001g0133a0001c0004t0001g0132a0002c0002t0003g0134others(2): Show | 5 | HG02258.hp1 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-8113A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27565788 | ||||||
chr16:27565918
|
T | A | 4 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-7983T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27565918 | ||||||
chr16:27566022
|
GT | G | 8 | a0001c0001t0001g0019a0001c0015t0001g0012a0001c0015t0001g0084others(5): Show | 8 | HG00741.hp2 HG01243.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-7861delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27566022 | |||||
chr16:27566030
|
T | G | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.8-7871T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27566030 | ||||||
chr16:27566399
|
G | T | 1 | a0001c0001t0004g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.8-7502G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27566399 | ||||||
chr16:27566805
|
G | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8-7096G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27566805 | ||||||
chr16:27566874
|
C | A | 2 | a0001c0028t0004g0109a0018c0025t0003g0111 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.8-7027C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27566874 | ||||||
chr16:27567138
|
G | A | 1 | a0001c0001t0004g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.8-6763G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27567138 | ||||||
chr16:27567871
|
G | A | 4 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-6030G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27567871 | ||||||
chr16:27567874
|
G | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG00408.hp2 HG01978.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-6027G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27567874 | ||||||
chr16:27567926
|
T | C | 1 | a0001c0001t0001g0006 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.8-5975T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27567926 | ||||||
chr16:27567999
|
A | G | 1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.8-5902A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27567999 | ||||||
chr16:27568323
|
C | T | 1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.8-5578C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27568323 | ||||||
chr16:27568715
|
G | A | 1 | a0001c0001t0004g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.8-5186G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27568715 | ||||||
chr16:27569263
|
T | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.8-4638T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27569263 | ||||||
chr16:27569280
|
T | C | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.8-4621T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27569280 | ||||||
chr16:27569339
|
C | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.8-4562C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27569339 | ||||||
chr16:27569391
|
A | G | 1 | a0017c0021t0001g0016 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.8-4510A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27569391 | ||||||
chr16:27569491
|
C | A | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.8-4410C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27569491 | ||||||
chr16:27569768
|
A | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.8-4133A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27569768 | ||||||
chr16:27570044
|
G | A | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.8-3857G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27570044 | ||||||
chr16:27570738
|
C | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.8-3163C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27570738 | ||||||
chr16:27570821
|
A | G | 1 | a0001c0001t0002g0040 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-3080A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27570821 | ||||||
chr16:27571280
|
G | A | 4 | a0004c0030t0005g0115a0007c0010t0002g0112a0007c0010t0002g0113others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-2621G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27571280 | ||||||
chr16:27571290
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.8-2611C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27571290 | ||||||
chr16:27571448
|
G | GA | 8 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(5): Show | 8 | HG01109.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-2439dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27571448 | |||||
chr16:27571448
|
G | GAA | 10 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(7): Show | 10 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.8-2440_8-2439dupAA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27571448 | |||||
chr16:27571602
|
G | A | 1 | a0003c0003t0002g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.8-2299G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27571602 | ||||||
chr16:27571682
|
G | A | 3 | a0003c0003t0002g0121a0003c0003t0002g0123a0003c0003t0002g0139 | 3 | HG01358.hp2 HG02683.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.8-2219G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27571682 | ||||||
chr16:27571772
|
C | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(3): Show | 6 | HG01358.hp1 HG02155.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.8-2129C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27571772 | ||||||
chr16:27571868
|
C | A | 2 | a0002c0002t0003g0097a0005c0006t0001g0058 | 2 | NA18971.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.8-2033C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27571868 | ||||||
chr16:27571987
|
G | GGT | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.8-1897_8-1896dupGT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27571987 | |||||
chr16:27571987
|
G | T | 3 | a0001c0011t0002g0152a0001c0015t0001g0012a0014c0019t0003g0100 | 3 | HG02109.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.8-1914G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27571987 | ||||||
chr16:27571989
|
T | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0093a0001c0028t0004g0109 | 3 | HG00741.hp1 HG02280.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.8-1912T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27571989 | ||||||
chr16:27572016
|
G | A | 3 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0052 | 3 | HG02055.hp1 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.8-1885G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27572016 | ||||||
chr16:27572085
|
A | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.8-1816A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27572085 | ||||||
chr16:27572261
|
A | T | 3 | a0001c0001t0002g0071a0001c0018t0011g0122a0002c0029t0003g0101 | 3 | HG01106.hp1 HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.8-1640A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27572261 | ||||||
chr16:27572302
|
T | A | 1 | a0001c0023t0001g0060 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.8-1599T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27572302 | ||||||
chr16:27572362
|
A | AAC | 15 | a0001c0008t0004g0026a0001c0008t0004g0041a0001c0008t0004g0079others(12): Show | 15 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.8-1503_8-1502dupCA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27572362 | |||||
chr16:27572362
|
A | AACAC | 5 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0020others(2): Show | 5 | HG02135.hp2 HG02155.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-1505_8-1502dupCA others(2): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27572362 | |||||
chr16:27572362
|
A | AACACAC | 22 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0133others(19): Show | 22 | HG00099.hp2 HG00741.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.8-1507_8-1502dupCA others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27572362 | |||||
chr16:27572362
|
A | AACACACA others(1): Show |
35 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0028others(32): Show | 35 | HG00140.hp2 HG01109.hp1 HG01515.hp2 others(32): Show |
intron_variant | MODIFIER | c.8-1509_8-1502dupCA others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27572362 | |||||
chr16:27572362
|
A | AACACACA others(3): Show |
23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(20): Show | 23 | HG00741.hp1 HG01106.hp2 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.8-1511_8-1502dupCA others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27572362 | |||||
chr16:27572362
|
A | AACACACA others(5): Show |
2 | a0001c0001t0001g0086a0018c0025t0003g0111 | 2 | HG00408.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.8-1513_8-1502dupCA others(10): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27572362 | |||||
chr16:27572362
|
A | AACACACA others(9): Show |
1 | a0001c0004t0002g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.8-1517_8-1502dupCA others(14): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27572362 | |||||
chr16:27572362
|
A | AACACACA others(11): Show |
1 | a0001c0001t0008g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8-1519_8-1502dupCA others(16): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27572362 | |||||
chr16:27572362
|
A | C | 5 | a0001c0001t0001g0038a0001c0001t0007g0091a0001c0024t0001g0078others(2): Show | 5 | HG02165.hp2 NA18986.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-1539A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27572362 | ||||||
chr16:27572362
|
AAC | A | 5 | a0002c0002t0003g0063a0002c0002t0003g0099a0002c0002t0003g0104others(2): Show | 5 | HG02074.hp1 NA18954.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-1503_8-1502delCA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr16 | 27572362 | |||||
chr16:27572423
|
G | A | 3 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151 | 3 | HG02145.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.8-1478G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27572423 | ||||||
chr16:27572523
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.8-1378G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27572523 | ||||||
chr16:27572600
|
T | C | 2 | a0001c0028t0004g0109a0018c0025t0003g0111 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.8-1301T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27572600 | ||||||
chr16:27572619
|
A | G | 4 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-1282A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27572619 | ||||||
chr16:27572760
|
A | G | 1 | a0001c0001t0004g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.8-1141A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27572760 | ||||||
chr16:27572774
|
G | A | 1 | a0001c0004t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.8-1127G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27572774 | ||||||
chr16:27572992
|
G | T | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.8-909G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27572992 | ||||||
chr16:27573568
|
A | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.8-333A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27573568 | ||||||
chr16:27573832
|
T | G | 4 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-69T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 1/27 | chr16 | 27573832 | ||||||
chr16:27574121
|
GTCACTTG others(6): Show |
G | 1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+195_63+207delCT others(11): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27574121 | |||||
chr16:27574448
|
A | G | 4 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+492A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27574448 | ||||||
chr16:27574507
|
T | C | 1 | a0002c0002t0003g0072 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.63+551T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27574507 | ||||||
chr16:27574558
|
C | CT | 9 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(6): Show | 9 | HG01109.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+627dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27574558 | |||||
chr16:27574558
|
CT | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.63+627delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27574558 | |||||
chr16:27574558
|
CTT | C | 5 | a0001c0001t0001g0082a0001c0028t0004g0109a0002c0002t0003g0063others(2): Show | 5 | HG02280.hp2 HG02886.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+626_63+627delTT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27574558 | |||||
chr16:27574784
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.63+828G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27574784 | ||||||
chr16:27574793
|
A | ACCTCAGG others(6): Show |
116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.63+837_63+838insCC others(11): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27574793 | ||||||
chr16:27574876
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.63+920C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27574876 | ||||||
chr16:27574896
|
G | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.63+940G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27574896 | ||||||
chr16:27574971
|
TC | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(4): Show | 7 | HG00408.hp2 HG01978.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+1021delC | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27574971 | |||||
chr16:27574977
|
C | G | 5 | a0001c0001t0001g0133a0001c0004t0001g0132a0002c0002t0003g0134others(2): Show | 5 | HG02258.hp1 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+1021C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27574977 | ||||||
chr16:27575082
|
G | A | 4 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+1126G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27575082 | ||||||
chr16:27575221
|
A | G | 5 | a0004c0007t0010g0108a0004c0007t0012g0106a0008c0016t0001g0076others(2): Show | 5 | HG02055.hp2 HG02451.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+1265A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27575221 | ||||||
chr16:27575396
|
C | T | 5 | a0004c0007t0010g0108a0004c0007t0012g0106a0008c0016t0001g0076others(2): Show | 5 | HG02055.hp2 HG02451.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+1440C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27575396 | ||||||
chr16:27575447
|
C | A | 4 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+1491C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27575447 | ||||||
chr16:27575759
|
A | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.63+1803A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27575759 | ||||||
chr16:27576222
|
T | C | 1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.63+2266T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27576222 | ||||||
chr16:27576509
|
C | G | 2 | a0003c0003t0002g0130a0003c0003t0002g0131 | 2 | HG01258.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.63+2553C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27576509 | ||||||
chr16:27576660
|
A | C | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+2704A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27576660 | ||||||
chr16:27576902
|
C | T | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.63+2946C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27576902 | ||||||
chr16:27577389
|
A | T | 1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.63+3433A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27577389 | ||||||
chr16:27577623
|
C | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.63+3667C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27577623 | ||||||
chr16:27577641
|
G | A | 4 | a0004c0030t0005g0115a0007c0010t0002g0112a0007c0010t0002g0113others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+3685G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27577641 | ||||||
chr16:27578120
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.63+4164A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27578120 | ||||||
chr16:27578558
|
G | A | 5 | a0001c0001t0001g0133a0001c0004t0001g0132a0002c0002t0003g0134others(2): Show | 5 | HG02258.hp1 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+4602G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27578558 | ||||||
chr16:27578770
|
G | A | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.63+4814G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27578770 | ||||||
chr16:27579135
|
G | A | 10 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(7): Show | 10 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+5179G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27579135 | ||||||
chr16:27579153
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.63+5197T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27579153 | ||||||
chr16:27579275
|
CTG | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0087 | 2 | HG02135.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.63+5322_63+5323del others(2): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27579275 | |||||
chr16:27579281
|
A | C | 1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+5325A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27579281 | ||||||
chr16:27579769
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.63+5813C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27579769 | ||||||
chr16:27580019
|
A | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.63+6063A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27580019 | ||||||
chr16:27580101
|
C | T | 2 | a0002c0002t0003g0065a0002c0002t0003g0066 | 2 | HG00408.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.63+6145C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27580101 | ||||||
chr16:27580127
|
G | A | 1 | a0003c0003t0001g0127 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.63+6171G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27580127 | ||||||
chr16:27580173
|
C | T | 1 | a0002c0002t0003g0102 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.63+6217C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27580173 | ||||||
chr16:27580244
|
T | G | 5 | a0001c0001t0001g0133a0001c0004t0001g0132a0002c0002t0003g0134others(2): Show | 5 | HG02258.hp1 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+6288T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27580244 | ||||||
chr16:27580569
|
C | T | 2 | a0001c0001t0001g0047a0003c0003t0002g0094 | 2 | HG01109.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.63+6613C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27580569 | ||||||
chr16:27580653
|
C | T | 1 | a0001c0015t0001g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.63+6697C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27580653 | ||||||
chr16:27580683
|
C | G | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.63+6727C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27580683 | ||||||
chr16:27580699
|
AT | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.63+6761delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27580699 | |||||
chr16:27580832
|
C | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.63+6876C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27580832 | ||||||
chr16:27580884
|
C | T | 4 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+6928C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27580884 | ||||||
chr16:27581086
|
G | A | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+7130G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27581086 | ||||||
chr16:27581468
|
C | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.63+7512C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27581468 | ||||||
chr16:27581486
|
C | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.63+7530C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27581486 | ||||||
chr16:27581503
|
C | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.63+7547C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27581503 | ||||||
chr16:27581624
|
C | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(111): Show | 114 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.63+7668C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27581624 | ||||||
chr16:27582006
|
G | C | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+8050G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27582006 | ||||||
chr16:27582079
|
G | A | 2 | a0001c0011t0002g0141a0001c0011t0002g0152 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.63+8123G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27582079 | ||||||
chr16:27582266
|
T | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.63+8310T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27582266 | ||||||
chr16:27582611
|
G | A | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+8655G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27582611 | ||||||
chr16:27582640
|
C | A | 1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.63+8684C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27582640 | ||||||
chr16:27582661
|
T | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.63+8705T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27582661 | ||||||
chr16:27582700
|
G | T | 1 | a0001c0001t0004g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.63+8744G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27582700 | ||||||
chr16:27582859
|
G | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.63+8903G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27582859 | ||||||
chr16:27582890
|
G | A | 4 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+8934G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27582890 | ||||||
chr16:27583104
|
T | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.63+9148T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27583104 | ||||||
chr16:27583453
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.63+9497G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27583453 | ||||||
chr16:27583625
|
C | T | 1 | a0001c0012t0002g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.63+9669C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27583625 | ||||||
chr16:27583702
|
G | A | 1 | a0015c0020t0004g0008 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.63+9746G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27583702 | ||||||
chr16:27583741
|
T | C | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.63+9785T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27583741 | ||||||
chr16:27583815
|
G | A | 1 | a0013c0027t0001g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.63+9859G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27583815 | ||||||
chr16:27584058
|
A | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.63+10102A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27584058 | ||||||
chr16:27584099
|
G | A | 1 | a0001c0001t0009g0055 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.63+10143G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27584099 | ||||||
chr16:27584291
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.63+10335C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27584291 | ||||||
chr16:27584590
|
T | TGA | 4 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+10635_63+10636d others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27584590 | |||||
chr16:27584727
|
G | T | 1 | a0001c0004t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.63+10771G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27584727 | ||||||
chr16:27585263
|
TCAAAAGA others(13): Show |
T | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+11308_63+11327d others(22): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27585263 | ||||||
chr16:27585284
|
A | T | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+11328A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27585284 | ||||||
chr16:27585288
|
TGGCGA | T | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+11335_63+11339d others(7): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27585288 | |||||
chr16:27585454
|
G | A | 1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.63+11498G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27585454 | ||||||
chr16:27585478
|
T | C | 1 | a0013c0027t0001g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.63+11522T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27585478 | ||||||
chr16:27585570
|
A | G | 1 | a0004c0007t0010g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.63+11614A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27585570 | ||||||
chr16:27585650
|
T | C | 1 | a0001c0001t0002g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.63+11694T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27585650 | ||||||
chr16:27586134
|
T | C | 18 | a0001c0012t0002g0137a0001c0012t0002g0143a0001c0024t0001g0078others(15): Show | 18 | HG00408.hp1 HG02074.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.63+12178T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27586134 | ||||||
chr16:27586519
|
A | G | 6 | a0001c0001t0001g0083a0001c0001t0006g0037a0001c0008t0004g0026others(3): Show | 6 | HG02109.hp1 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+12563A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27586519 | ||||||
chr16:27586785
|
C | T | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.63+12829C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27586785 | ||||||
chr16:27586828
|
C | CA | 26 | a0001c0001t0001g0054a0001c0001t0001g0083a0001c0012t0002g0137others(23): Show | 26 | HG00408.hp1 HG02056.hp1 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+12885dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27586828 | |||||
chr16:27586850
|
C | A | 4 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+12894C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27586850 | ||||||
chr16:27586965
|
A | G | 1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+13009A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27586965 | ||||||
chr16:27587170
|
G | C | 6 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(3): Show | 6 | HG02970.hp1 HG03098.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+13214G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27587170 | ||||||
chr16:27587280
|
C | T | 2 | a0003c0003t0002g0126a0003c0003t0002g0129 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.63+13324C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27587280 | ||||||
chr16:27587484
|
C | T | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+13528C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27587484 | ||||||
chr16:27587818
|
T | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.63+13862T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27587818 | ||||||
chr16:27588009
|
G | A | 14 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(11): Show | 14 | HG01109.hp2 HG02896.hp1 HG02897.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+14053G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27588009 | ||||||
chr16:27588129
|
C | A | 1 | a0001c0024t0001g0078 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.63+14173C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27588129 | ||||||
chr16:27588171
|
T | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.63+14215T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27588171 | ||||||
chr16:27588380
|
A | G | 1 | a0001c0001t0004g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.63+14424A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27588380 | ||||||
chr16:27588878
|
CT | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(123): Show | 126 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.63+14943delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27588878 | |||||
chr16:27589070
|
AT | A | 6 | a0001c0001t0001g0133a0001c0004t0001g0132a0002c0002t0003g0098others(3): Show | 6 | HG02258.hp1 HG02965.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+15129delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27589070 | |||||
chr16:27589098
|
G | T | 1 | a0004c0007t0001g0075 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.63+15142G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27589098 | ||||||
chr16:27589510
|
A | G | 1 | a0015c0020t0004g0008 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.63+15554A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27589510 | ||||||
chr16:27589754
|
A | G | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+15798A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27589754 | ||||||
chr16:27589928
|
C | T | 10 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(7): Show | 10 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+15972C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27589928 | ||||||
chr16:27590379
|
G | T | 1 | a0001c0001t0004g0025 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.63+16423G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27590379 | ||||||
chr16:27590647
|
G | T | 1 | a0002c0002t0003g0098 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.63+16691G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27590647 | ||||||
chr16:27590884
|
A | G | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.63+16928A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27590884 | ||||||
chr16:27590904
|
T | C | 1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.63+16948T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27590904 | ||||||
chr16:27590930
|
G | T | 3 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105 | 3 | HG02615.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.63+16974G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27590930 | ||||||
chr16:27590982
|
G | A | 1 | a0001c0001t0004g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.63+17026G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27590982 | ||||||
chr16:27591270
|
C | T | 4 | a0004c0030t0005g0115a0007c0010t0002g0112a0007c0010t0002g0113others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+17314C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27591270 | ||||||
chr16:27591394
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.63+17438A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27591394 | ||||||
chr16:27591416
|
C | T | 3 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151 | 3 | HG02145.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.63+17460C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27591416 | ||||||
chr16:27591430
|
G | A | 1 | a0015c0020t0004g0008 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.63+17474G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27591430 | ||||||
chr16:27591435
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(1): Show | 4 | HG01358.hp1 HG02273.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+17479G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27591435 | ||||||
chr16:27591494
|
C | A | 1 | a0015c0020t0004g0008 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.63+17538C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27591494 | ||||||
chr16:27591704
|
C | T | 2 | a0001c0001t0002g0071a0002c0029t0003g0101 | 2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.63+17748C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27591704 | ||||||
chr16:27591705
|
G | T | 1 | a0001c0001t0001g0009 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.63+17749G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27591705 | ||||||
chr16:27591855
|
G | GC | 4 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+17900dupC | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27591855 | |||||
chr16:27591961
|
G | C | 1 | a0003c0003t0002g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.63+18005G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27591961 | ||||||
chr16:27592098
|
C | T | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.63+18142C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27592098 | ||||||
chr16:27592129
|
T | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0092 | 3 | HG02056.hp2 HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.63+18173T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27592129 | ||||||
chr16:27592270
|
CT | C | 7 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0002g0027others(4): Show | 7 | HG00099.hp2 HG01106.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+18344delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27592270 | |||||
chr16:27592270
|
CTT | C | 54 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(51): Show | 54 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.63+18343_63+18344d others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27592270 | |||||
chr16:27592270
|
CTTT | C | 45 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0021others(42): Show | 45 | HG00741.hp2 HG01243.hp1 HG01258.hp1 others(42): Show |
intron_variant | MODIFIER | c.63+18342_63+18344d others(5): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27592270 | |||||
chr16:27592270
|
CTTTT | C | 17 | a0001c0001t0009g0055a0001c0008t0004g0026a0001c0008t0004g0079others(14): Show | 17 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.63+18341_63+18344d others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27592270 | |||||
chr16:27592270
|
CTTTTT | C | 6 | a0001c0001t0001g0133a0001c0004t0001g0132a0002c0002t0003g0134others(3): Show | 6 | HG01515.hp2 HG02258.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+18340_63+18344d others(7): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27592270 | |||||
chr16:27592270
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.63+18334_63+18344d others(13): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27592270 | |||||
chr16:27592270
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0004g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.63+18332_63+18344d others(15): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27592270 | |||||
chr16:27592551
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.63+18595G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27592551 | ||||||
chr16:27592621
|
C | A | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+18665C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27592621 | ||||||
chr16:27592962
|
A | G | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+19006A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27592962 | ||||||
chr16:27593115
|
A | C | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+19159A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27593115 | ||||||
chr16:27593190
|
A | C | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+19234A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27593190 | ||||||
chr16:27593424
|
G | A | 1 | a0001c0001t0004g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.63+19468G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27593424 | ||||||
chr16:27593752
|
T | C | 1 | a0006c0009t0001g0096 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.63+19796T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27593752 | ||||||
chr16:27593772
|
G | T | 6 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(3): Show | 6 | HG02970.hp1 HG03098.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+19816G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27593772 | ||||||
chr16:27593778
|
G | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.63+19822G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27593778 | ||||||
chr16:27594033
|
A | G | 3 | a0004c0034t0005g0119a0011c0017t0005g0150a0011c0017t0005g0151 | 3 | HG02145.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.63+20077A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27594033 | ||||||
chr16:27594238
|
T | C | 1 | a0003c0003t0002g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.63+20282T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27594238 | ||||||
chr16:27594375
|
T | G | 2 | a0001c0001t0002g0071a0002c0029t0003g0101 | 2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.63+20419T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27594375 | ||||||
chr16:27594376
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.63+20420C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27594376 | ||||||
chr16:27594480
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.63+20524C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27594480 | ||||||
chr16:27594512
|
C | A | 1 | a0001c0001t0001g0083 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.63+20556C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27594512 | ||||||
chr16:27594728
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.63+20772C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27594728 | ||||||
chr16:27594864
|
T | C | 1 | a0001c0001t0002g0011 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.63+20908T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27594864 | ||||||
chr16:27595221
|
C | T | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+21265C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27595221 | ||||||
chr16:27595692
|
G | A | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.63+21736G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27595692 | ||||||
chr16:27595923
|
A | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.63+21967A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27595923 | ||||||
chr16:27595967
|
G | A | 1 | a0009c0014t0001g0043 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.63+22011G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27595967 | ||||||
chr16:27596009
|
G | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.63+22053G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27596009 | ||||||
chr16:27596342
|
T | A | 10 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(7): Show | 10 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-22083T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27596342 | ||||||
chr16:27596718
|
C | T | 1 | a0001c0001t0004g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.64-21707C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27596718 | ||||||
chr16:27597058
|
A | G | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.64-21367A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27597058 | ||||||
chr16:27597258
|
A | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.64-21167A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27597258 | ||||||
chr16:27597402
|
CT | C | 8 | a0001c0004t0001g0132a0001c0011t0002g0141a0001c0011t0002g0152others(5): Show | 8 | HG01243.hp2 HG02717.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-20994delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27597402 | |||||
chr16:27597402
|
CTT | C | 44 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00408.hp1 HG00741.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.64-20995_64-20994d others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27597402 | |||||
chr16:27597402
|
CTTT | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(62): Show | 65 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.64-20996_64-20994d others(5): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27597402 | |||||
chr16:27597402
|
CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0002g0014a0001c0001t0002g0027a0001c0001t0002g0046others(2): Show | 5 | HG01358.hp2 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-21003_64-20994d others(12): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27597402 | |||||
chr16:27597402
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.64-21004_64-20994d others(13): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27597402 | |||||
chr16:27597402
|
CTTTTTTT others(8): Show |
C | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-21008_64-20994d others(17): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27597402 | |||||
chr16:27598019
|
G | C | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.64-20406G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27598019 | ||||||
chr16:27598090
|
G | A | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.64-20335G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27598090 | ||||||
chr16:27598198
|
G | A | 2 | a0001c0001t0002g0071a0002c0029t0003g0101 | 2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.64-20227G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27598198 | ||||||
chr16:27598222
|
C | T | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.64-20203C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27598222 | ||||||
chr16:27598243
|
C | CA | 35 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0087others(32): Show | 35 | HG00408.hp1 HG02055.hp2 HG02074.hp1 others(32): Show |
intron_variant | MODIFIER | c.64-20169dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27598243 | |||||
chr16:27598243
|
C | CAA | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.64-20170_64-20169d others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27598243 | |||||
chr16:27598369
|
G | A | 3 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0136 | 3 | HG02965.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64-20056G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27598369 | ||||||
chr16:27598722
|
T | C | 1 | a0017c0021t0001g0016 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.64-19703T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27598722 | ||||||
chr16:27598767
|
A | G | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-19658A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27598767 | ||||||
chr16:27598773
|
G | T | 1 | a0001c0004t0001g0042 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.64-19652G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27598773 | ||||||
chr16:27599013
|
G | A | 1 | a0002c0002t0003g0099 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.64-19412G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27599013 | ||||||
chr16:27599050
|
G | A | 1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-19375G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27599050 | ||||||
chr16:27599192
|
C | G | 1 | a0005c0006t0001g0085 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.64-19233C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27599192 | ||||||
chr16:27599264
|
T | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.64-19161T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27599264 | ||||||
chr16:27599342
|
C | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.64-19083C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27599342 | ||||||
chr16:27599504
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.64-18921C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27599504 | ||||||
chr16:27599508
|
G | T | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.64-18917G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27599508 | ||||||
chr16:27599740
|
C | T | 2 | a0001c0028t0004g0109a0018c0025t0003g0111 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.64-18685C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27599740 | ||||||
chr16:27599823
|
C | T | 14 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(11): Show | 14 | HG01109.hp2 HG02896.hp1 HG02897.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-18602C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27599823 | ||||||
chr16:27599911
|
C | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-18514C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27599911 | ||||||
chr16:27599958
|
C | T | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-18467C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27599958 | ||||||
chr16:27600066
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.64-18359G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27600066 | ||||||
chr16:27600340
|
T | C | 11 | a0001c0001t0001g0053a0001c0001t0001g0083a0001c0001t0004g0024others(8): Show | 11 | HG01258.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-18085T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27600340 | ||||||
chr16:27600732
|
CT | C | 6 | a0001c0001t0001g0006a0001c0001t0002g0040a0001c0004t0002g0069others(3): Show | 6 | HG00741.hp2 HG01515.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-17678delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27600732 | |||||
chr16:27600761
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.64-17664A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27600761 | ||||||
chr16:27600791
|
G | T | 1 | a0004c0034t0005g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64-17634G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27600791 | ||||||
chr16:27600855
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.64-17570G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27600855 | ||||||
chr16:27600861
|
C | G | 1 | a0001c0001t0002g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.64-17564C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27600861 | ||||||
chr16:27600958
|
C | A | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.64-17467C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27600958 | ||||||
chr16:27601131
|
T | C | 1 | a0001c0001t0001g0010 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.64-17294T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27601131 | ||||||
chr16:27601484
|
G | A | 10 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(7): Show | 10 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-16941G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27601484 | ||||||
chr16:27601485
|
G | C | 1 | a0003c0003t0002g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.64-16940G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27601485 | ||||||
chr16:27601593
|
A | G | 12 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(9): Show | 12 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-16832A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27601593 | ||||||
chr16:27601981
|
C | G | 4 | a0001c0004t0001g0132a0002c0002t0003g0134a0002c0002t0003g0135others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-16444C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27601981 | ||||||
chr16:27602128
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.64-16297T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27602128 | ||||||
chr16:27602415
|
A | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.64-16010A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27602415 | ||||||
chr16:27602444
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.64-15981G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27602444 | ||||||
chr16:27602641
|
T | C | 2 | a0001c0012t0002g0137a0001c0012t0002g0143 | 2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.64-15784T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27602641 | ||||||
chr16:27602707
|
C | CT | 12 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(9): Show | 12 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-15709dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27602707 | |||||
chr16:27603037
|
G | T | 12 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(9): Show | 12 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-15388G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27603037 | ||||||
chr16:27603569
|
G | A | 1 | a0015c0020t0004g0008 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.64-14856G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27603569 | ||||||
chr16:27603737
|
CT | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(116): Show | 119 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.64-14671delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27603737 | |||||
chr16:27603824
|
C | G | 1 | a0001c0001t0004g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.64-14601C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27603824 | ||||||
chr16:27603974
|
C | T | 2 | a0007c0010t0002g0112a0007c0010t0002g0113 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.64-14451C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27603974 | ||||||
chr16:27604211
|
G | A | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-14214G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27604211 | ||||||
chr16:27604292
|
G | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.64-14133G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27604292 | ||||||
chr16:27604524
|
C | T | 2 | a0003c0003t0002g0126a0003c0003t0002g0129 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.64-13901C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27604524 | ||||||
chr16:27605537
|
G | A | 1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.64-12888G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27605537 | ||||||
chr16:27605906
|
G | T | 1 | a0009c0014t0001g0018 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64-12519G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27605906 | ||||||
chr16:27605954
|
A | C | 6 | a0001c0001t0001g0083a0001c0001t0006g0037a0001c0008t0004g0026others(3): Show | 6 | HG02109.hp1 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-12471A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27605954 | ||||||
chr16:27605966
|
T | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.64-12459T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27605966 | ||||||
chr16:27606002
|
C | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.64-12423C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27606002 | ||||||
chr16:27606116
|
C | T | 13 | a0001c0001t0001g0095a0004c0007t0001g0074a0004c0007t0001g0075others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-12309C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27606116 | ||||||
chr16:27606462
|
G | T | 1 | a0003c0003t0002g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64-11963G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27606462 | ||||||
chr16:27606478
|
T | TAC | 6 | a0001c0001t0001g0053a0001c0028t0004g0109a0004c0030t0005g0115others(3): Show | 6 | HG02280.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-11927_64-11926d others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27606478 | |||||
chr16:27606478
|
TAC | T | 12 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(9): Show | 12 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-11927_64-11926d others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27606478 | |||||
chr16:27606484
|
C | T | 12 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(9): Show | 12 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-11941C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27606484 | ||||||
chr16:27606500
|
G | C | 1 | a0001c0008t0004g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-11925G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27606500 | ||||||
chr16:27606500
|
GACACACA others(7): Show |
G | 1 | a0001c0001t0001g0089 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.64-11900_64-11887d others(16): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27606500 | |||||
chr16:27606548
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.64-11877G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27606548 | ||||||
chr16:27606690
|
G | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.64-11735G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27606690 | ||||||
chr16:27606732
|
CT | C | 13 | a0002c0002t0003g0063a0004c0007t0001g0074a0004c0007t0001g0075others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-11680delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27606732 | |||||
chr16:27606848
|
G | A | 1 | a0005c0006t0001g0013 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.64-11577G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27606848 | ||||||
chr16:27607431
|
C | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.64-10994C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27607431 | ||||||
chr16:27607537
|
G | A | 12 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(9): Show | 12 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-10888G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27607537 | ||||||
chr16:27607557
|
G | A | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.64-10868G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27607557 | ||||||
chr16:27607594
|
C | CT | 10 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(7): Show | 10 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-10810dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27607594 | |||||
chr16:27607594
|
CT | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 101 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.64-10810delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27607594 | |||||
chr16:27607594
|
CTTT | C | 13 | a0001c0001t0001g0020a0004c0007t0001g0074a0004c0007t0001g0075others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-10812_64-10810d others(5): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27607594 | |||||
chr16:27607661
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.64-10764A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27607661 | ||||||
chr16:27607688
|
C | T | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.64-10737C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27607688 | ||||||
chr16:27607726
|
T | C | 11 | a0001c0001t0001g0019a0001c0015t0001g0012a0001c0015t0001g0084others(8): Show | 11 | HG00741.hp2 HG01243.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-10699T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27607726 | ||||||
chr16:27607782
|
T | G | 1 | a0001c0004t0001g0116 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.64-10643T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27607782 | ||||||
chr16:27608178
|
T | G | 10 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(7): Show | 10 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-10247T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27608178 | ||||||
chr16:27608226
|
C | CT | 12 | a0001c0001t0001g0021a0001c0001t0001g0028a0001c0001t0001g0083others(9): Show | 12 | HG00741.hp1 HG01106.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-10177dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27608226 | |||||
chr16:27608226
|
CT | C | 5 | a0001c0001t0002g0040a0001c0001t0002g0046a0001c0023t0001g0060others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-10177delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27608226 | |||||
chr16:27608335
|
A | G | 1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.64-10090A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27608335 | ||||||
chr16:27608356
|
A | G | 6 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(3): Show | 6 | HG02970.hp1 HG03098.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-10069A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27608356 | ||||||
chr16:27608399
|
C | CT | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(103): Show | 106 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.64-10006dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27608399 | |||||
chr16:27608399
|
C | CTT | 14 | a0001c0001t0001g0057a0002c0029t0003g0101a0004c0007t0001g0074others(11): Show | 14 | HG00140.hp2 HG01243.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-10007_64-10006d others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27608399 | |||||
chr16:27608461
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.64-9964G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27608461 | ||||||
chr16:27608571
|
C | G | 12 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(9): Show | 12 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-9854C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27608571 | ||||||
chr16:27608653
|
G | C | 1 | a0001c0001t0004g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.64-9772G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27608653 | ||||||
chr16:27608774
|
A | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.64-9651A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27608774 | ||||||
chr16:27608799
|
G | A | 1 | a0002c0002t0003g0098 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.64-9626G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27608799 | ||||||
chr16:27608844
|
G | A | 12 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(9): Show | 12 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-9581G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27608844 | ||||||
chr16:27609378
|
C | CT | 11 | a0001c0001t0004g0052a0001c0005t0001g0144a0001c0005t0001g0146others(8): Show | 11 | HG01361.hp1 HG02055.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-9017dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27609378 | |||||
chr16:27609378
|
CT | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(64): Show | 67 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.64-9017delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27609378 | |||||
chr16:27609378
|
CTT | C | 32 | a0001c0001t0001g0006a0001c0001t0002g0071a0001c0004t0001g0117others(29): Show | 32 | HG00408.hp1 HG02055.hp2 HG02074.hp1 others(29): Show |
intron_variant | MODIFIER | c.64-9018_64-9017del others(2): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27609378 | |||||
chr16:27609454
|
G | A | 10 | a0001c0001t0001g0015a0004c0007t0001g0074a0004c0007t0001g0075others(7): Show | 10 | HG02055.hp2 HG02165.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-8971G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27609454 | ||||||
chr16:27609459
|
C | G | 1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.64-8966C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27609459 | ||||||
chr16:27609632
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.64-8793C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27609632 | ||||||
chr16:27609664
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.64-8761A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27609664 | ||||||
chr16:27609680
|
G | A | 6 | a0001c0001t0001g0053a0001c0001t0002g0014a0001c0001t0002g0027others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-8745G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27609680 | ||||||
chr16:27609695
|
A | AT | 14 | a0001c0001t0001g0093a0001c0001t0004g0005a0001c0004t0001g0116others(11): Show | 14 | HG00741.hp1 HG01109.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.64-8715dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27609695 | |||||
chr16:27609695
|
A | ATT | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-8716_64-8715dup others(2): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27609695 | |||||
chr16:27609695
|
AT | A | 8 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(5): Show | 8 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-8715delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27609695 | |||||
chr16:27609771
|
A | G | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-8654A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27609771 | ||||||
chr16:27609873
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG01358.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.64-8552G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27609873 | ||||||
chr16:27609984
|
G | A | 1 | a0006c0009t0001g0036 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.64-8441G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27609984 | ||||||
chr16:27610042
|
G | A | 2 | a0011c0017t0005g0150a0011c0017t0005g0151 | 2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.64-8383G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27610042 | ||||||
chr16:27610242
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.64-8183C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27610242 | ||||||
chr16:27610376
|
C | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.64-8049C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27610376 | ||||||
chr16:27610395
|
T | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.64-8030T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27610395 | ||||||
chr16:27610611
|
G | A | 2 | a0001c0028t0004g0109a0018c0025t0003g0111 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.64-7814G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27610611 | ||||||
chr16:27610708
|
T | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-7717T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27610708 | ||||||
chr16:27611246
|
G | A | 9 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(6): Show | 9 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-7179G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27611246 | ||||||
chr16:27611361
|
T | G | 1 | a0001c0001t0001g0031 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.64-7064T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27611361 | ||||||
chr16:27611411
|
G | C | 1 | a0002c0002t0003g0072 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.64-7014G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27611411 | ||||||
chr16:27611483
|
C | T | 2 | a0001c0028t0004g0109a0018c0025t0003g0111 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.64-6942C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27611483 | ||||||
chr16:27611494
|
A | G | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-6931A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27611494 | ||||||
chr16:27611551
|
G | A | 1 | a0003c0003t0002g0120 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.64-6874G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27611551 | ||||||
chr16:27611848
|
A | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-6577A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27611848 | ||||||
chr16:27611853
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0054 | 2 | NA18959.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.64-6572C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27611853 | ||||||
chr16:27612226
|
A | ACC | 2 | a0001c0001t0001g0030a0001c0001t0001g0092 | 2 | HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.64-6199_64-6198ins others(2): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27612226 | ||||||
chr16:27612228
|
GT | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0092 | 2 | HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.64-6195delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27612228 | |||||
chr16:27612357
|
A | G | 2 | a0001c0004t0002g0070a0001c0004t0002g0073 | 2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.64-6068A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27612357 | ||||||
chr16:27612948
|
A | T | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(4): Show | 7 | HG00099.hp2 HG01358.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-5477A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27612948 | ||||||
chr16:27613104
|
C | CAAAAAAA | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-5320_64-5314dup others(7): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27613104 | |||||
chr16:27613561
|
AATGGTT | A | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-4860_64-4855del others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27613561 | |||||
chr16:27613582
|
G | T | 1 | a0008c0016t0001g0077 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.64-4843G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27613582 | ||||||
chr16:27613696
|
G | A | 11 | a0001c0001t0001g0083a0001c0001t0004g0024a0001c0001t0004g0025others(8): Show | 11 | HG01258.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-4729G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27613696 | ||||||
chr16:27613740
|
A | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0092 | 3 | HG02056.hp2 HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.64-4685A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27613740 | ||||||
chr16:27613834
|
C | T | 1 | a0015c0020t0004g0008 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.64-4591C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27613834 | ||||||
chr16:27613839
|
C | T | 1 | a0004c0030t0005g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.64-4586C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27613839 | ||||||
chr16:27613844
|
G | A | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-4581G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27613844 | ||||||
chr16:27613925
|
G | A | 3 | a0003c0003t0002g0121a0003c0003t0002g0123a0003c0003t0002g0139 | 3 | HG01358.hp2 HG02683.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.64-4500G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27613925 | ||||||
chr16:27614080
|
A | AT | 10 | a0001c0001t0001g0053a0001c0001t0001g0133a0001c0001t0002g0014others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-4332dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27614080 | |||||
chr16:27614114
|
G | C | 2 | a0001c0004t0001g0116a0001c0004t0001g0118 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.64-4311G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27614114 | ||||||
chr16:27614180
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.64-4245C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27614180 | ||||||
chr16:27614268
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.64-4157C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27614268 | ||||||
chr16:27614428
|
T | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-3997T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27614428 | ||||||
chr16:27614459
|
C | G | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.64-3966C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27614459 | ||||||
chr16:27614490
|
T | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-3935T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27614490 | ||||||
chr16:27615034
|
C | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-3391C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27615034 | ||||||
chr16:27615153
|
G | A | 1 | a0005c0006t0001g0085 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.64-3272G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27615153 | ||||||
chr16:27615274
|
A | G | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-3151A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27615274 | ||||||
chr16:27615293
|
C | CT | 8 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0052others(5): Show | 8 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-3116dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27615293 | |||||
chr16:27615293
|
CT | C | 7 | a0001c0001t0001g0021a0001c0001t0002g0033a0001c0008t0004g0079others(4): Show | 7 | HG01515.hp1 HG02486.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-3116delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27615293 | |||||
chr16:27615457
|
C | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.64-2968C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27615457 | ||||||
chr16:27615674
|
T | C | 6 | a0005c0006t0001g0013a0005c0006t0001g0058a0005c0006t0001g0059others(3): Show | 6 | HG00741.hp2 HG01243.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-2751T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27615674 | ||||||
chr16:27616134
|
G | A | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.64-2291G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27616134 | ||||||
chr16:27616137
|
C | A | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-2288C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27616137 | ||||||
chr16:27616288
|
G | A | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-2137G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27616288 | ||||||
chr16:27616430
|
A | G | 2 | a0001c0001t0001g0047a0003c0003t0002g0094 | 2 | HG01109.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.64-1995A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27616430 | ||||||
chr16:27616499
|
G | A | 9 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(6): Show | 9 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-1926G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27616499 | ||||||
chr16:27616641
|
C | T | 1 | a0001c0001t0007g0091 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.64-1784C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27616641 | ||||||
chr16:27616778
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0054 | 2 | NA18959.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.64-1647A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27616778 | ||||||
chr16:27616886
|
CTAAAAAA | C | 4 | a0001c0004t0001g0132a0002c0002t0003g0134a0002c0002t0003g0135others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-1538_64-1532del others(7): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27616886 | ||||||
chr16:27616887
|
T | TAA | 8 | a0003c0003t0002g0120a0003c0003t0002g0139a0004c0007t0001g0074others(5): Show | 8 | HG00140.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-1501_64-1500dup others(2): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27616887 | |||||
chr16:27616887
|
TA | T | 7 | a0001c0005t0001g0145a0001c0005t0001g0146a0001c0005t0002g0149others(4): Show | 7 | HG01106.hp1 HG01243.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-1500delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27616887 | |||||
chr16:27616887
|
TAA | T | 6 | a0001c0001t0001g0082a0001c0005t0001g0144a0001c0005t0002g0147others(3): Show | 6 | HG02056.hp1 HG03139.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-1501_64-1500del others(2): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27616887 | |||||
chr16:27616887
|
TAAA | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0019a0005c0006t0001g0059others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-1502_64-1500del others(3): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27616887 | |||||
chr16:27616887
|
TAAAA | T | 11 | a0001c0001t0001g0003a0001c0001t0002g0034a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01358.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-1503_64-1500del others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27616887 | |||||
chr16:27616887
|
TAAAAA | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.64-1504_64-1500del others(5): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27616887 | |||||
chr16:27616887
|
TAAAAAA | T | 43 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0020others(40): Show | 43 | HG00408.hp2 HG00741.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.64-1505_64-1500del others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27616887 | |||||
chr16:27616887
|
TAAAAAAA | T | 19 | a0001c0001t0002g0033a0001c0001t0002g0071a0001c0004t0001g0116others(16): Show | 19 | HG00408.hp1 HG02132.hp2 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-1506_64-1500del others(7): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27616887 | |||||
chr16:27616887
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-1512_64-1500del others(13): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27616887 | |||||
chr16:27616887
|
TAAAAAAA others(15): Show |
T | 1 | a0003c0003t0002g0140 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.64-1521_64-1500del others(22): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr16 | 27616887 | |||||
chr16:27616894
|
A | C | 4 | a0001c0004t0001g0132a0002c0002t0003g0134a0002c0002t0003g0135others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-1531A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27616894 | ||||||
chr16:27617117
|
G | C | 4 | a0001c0004t0001g0132a0002c0002t0003g0134a0002c0002t0003g0135others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-1308G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27617117 | ||||||
chr16:27617254
|
C | T | 9 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(6): Show | 9 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-1171C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27617254 | ||||||
chr16:27617396
|
G | T | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-1029G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27617396 | ||||||
chr16:27617476
|
T | C | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-949T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27617476 | ||||||
chr16:27617542
|
C | T | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.64-883C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27617542 | ||||||
chr16:27617727
|
G | A | 4 | a0003c0003t0002g0125a0003c0003t0002g0130a0003c0003t0002g0131others(1): Show | 4 | HG01258.hp2 HG01361.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-698G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27617727 | ||||||
chr16:27617841
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.64-584C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27617841 | ||||||
chr16:27617946
|
C | T | 1 | a0013c0027t0001g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64-479C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27617946 | ||||||
chr16:27618274
|
A | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-151A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27618274 | ||||||
chr16:27618340
|
G | C | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(121): Show | 124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.64-85G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27618340 | ||||||
chr16:27618348
|
G | A | 2 | a0003c0003t0002g0126a0003c0003t0002g0129 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.64-77G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 2/27 | chr16 | 27618348 | ||||||
chr16:27618517
|
C | T | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.140+16C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27618517 | ||||||
chr16:27618712
|
C | T | 1 | a0002c0002t0003g0072 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.140+211C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27618712 | ||||||
chr16:27618842
|
T | C | 1 | a0001c0001t0001g0010 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.140+341T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27618842 | ||||||
chr16:27618908
|
T | C | 3 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0052 | 3 | HG02055.hp1 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.140+407T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27618908 | ||||||
chr16:27619020
|
G | C | 1 | a0002c0002t0003g0110 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.140+519G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27619020 | ||||||
chr16:27619235
|
G | T | 2 | a0001c0004t0001g0116a0001c0004t0001g0118 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.140+734G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27619235 | ||||||
chr16:27619377
|
C | G | 2 | a0002c0002t0003g0068a0002c0002t0003g0110 | 2 | HG02135.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.140+876C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27619377 | ||||||
chr16:27619422
|
G | A | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.140+921G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27619422 | ||||||
chr16:27619440
|
G | A | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.140+939G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27619440 | ||||||
chr16:27619717
|
C | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.140+1216C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27619717 | ||||||
chr16:27619729
|
C | A | 1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.140+1228C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27619729 | ||||||
chr16:27619797
|
C | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.140+1296C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27619797 | ||||||
chr16:27619901
|
C | T | 18 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(15): Show | 18 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.140+1400C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27619901 | ||||||
chr16:27619950
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.140+1449A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27619950 | ||||||
chr16:27620601
|
G | A | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.140+2100G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27620601 | ||||||
chr16:27620738
|
AG | A | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.140+2243delG | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr16 | 27620738 | |||||
chr16:27620745
|
A | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.140+2244A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27620745 | ||||||
chr16:27620917
|
C | G | 1 | a0001c0001t0007g0091 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.140+2416C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27620917 | ||||||
chr16:27621114
|
A | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.140+2613A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27621114 | ||||||
chr16:27621188
|
T | C | 4 | a0001c0004t0001g0132a0002c0002t0003g0134a0002c0002t0003g0135others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+2687T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27621188 | ||||||
chr16:27621390
|
C | T | 2 | a0001c0001t0004g0025a0001c0001t0004g0052 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.140+2889C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27621390 | ||||||
chr16:27621401
|
A | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.140+2900A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27621401 | ||||||
chr16:27621435
|
A | G | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.140+2934A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27621435 | ||||||
chr16:27621465
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.140+2964C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27621465 | ||||||
chr16:27621508
|
C | T | 9 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(6): Show | 9 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.140+3007C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27621508 | ||||||
chr16:27621559
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.140+3058C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27621559 | ||||||
chr16:27621649
|
C | T | 1 | a0001c0001t0009g0055 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.140+3148C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27621649 | ||||||
chr16:27621744
|
A | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.140+3243A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27621744 | ||||||
chr16:27621784
|
TG | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.140+3290delG | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr16 | 27621784 | |||||
chr16:27622054
|
C | A | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(123): Show | 126 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.140+3553C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27622054 | ||||||
chr16:27622167
|
T | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.140+3666T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27622167 | ||||||
chr16:27622247
|
G | A | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.140+3746G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27622247 | ||||||
chr16:27622356
|
C | A | 1 | a0001c0001t0001g0039 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.140+3855C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27622356 | ||||||
chr16:27622400
|
T | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.140+3899T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27622400 | ||||||
chr16:27622503
|
G | A | 1 | a0001c0012t0002g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.140+4002G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27622503 | ||||||
chr16:27622789
|
C | A | 1 | a0001c0001t0001g0093 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.140+4288C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27622789 | ||||||
chr16:27622820
|
T | C | 1 | a0001c0012t0002g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.140+4319T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27622820 | ||||||
chr16:27622941
|
A | T | 1 | a0001c0001t0001g0023 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.140+4440A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27622941 | ||||||
chr16:27623290
|
G | A | 6 | a0001c0001t0001g0083a0001c0001t0006g0037a0001c0008t0004g0026others(3): Show | 6 | HG02109.hp1 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+4789G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27623290 | ||||||
chr16:27623793
|
G | A | 1 | a0001c0005t0002g0147 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.141-4868G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27623793 | ||||||
chr16:27623839
|
A | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.141-4822A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27623839 | ||||||
chr16:27623910
|
A | G | 2 | a0010c0013t0003g0061a0010c0013t0003g0103 | 2 | NA19000.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.141-4751A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27623910 | ||||||
chr16:27624062
|
G | A | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-4599G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27624062 | ||||||
chr16:27624333
|
C | T | 1 | a0001c0001t0004g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.141-4328C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27624333 | ||||||
chr16:27624436
|
A | T | 1 | a0001c0001t0001g0039 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.141-4225A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27624436 | ||||||
chr16:27624441
|
G | A | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.141-4220G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27624441 | ||||||
chr16:27624519
|
A | G | 19 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0020others(16): Show | 19 | HG00408.hp2 HG00741.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.141-4142A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27624519 | ||||||
chr16:27624524
|
C | T | 1 | a0001c0005t0002g0149 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.141-4137C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27624524 | ||||||
chr16:27624651
|
A | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.141-4010A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27624651 | ||||||
chr16:27625855
|
CT | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.141-2795delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr16 | 27625855 | |||||
chr16:27625998
|
C | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.141-2663C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27625998 | ||||||
chr16:27626247
|
A | G | 1 | a0001c0001t0001g0009 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.141-2414A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27626247 | ||||||
chr16:27626576
|
A | G | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(121): Show | 124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.141-2085A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27626576 | ||||||
chr16:27626888
|
C | G | 2 | a0001c0012t0002g0137a0001c0012t0002g0143 | 2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.141-1773C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27626888 | ||||||
chr16:27626919
|
C | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.141-1742C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27626919 | ||||||
chr16:27626964
|
CA | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.141-1681delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr16 | 27626964 | |||||
chr16:27627139
|
T | G | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.141-1522T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27627139 | ||||||
chr16:27627370
|
A | T | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.141-1291A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27627370 | ||||||
chr16:27627567
|
A | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.141-1094A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27627567 | ||||||
chr16:27627616
|
A | G | 2 | a0003c0003t0002g0126a0003c0003t0002g0129 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.141-1045A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27627616 | ||||||
chr16:27627725
|
T | C | 1 | a0005c0006t0001g0085 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.141-936T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27627725 | ||||||
chr16:27628317
|
C | T | 1 | a0011c0017t0005g0151 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.141-344C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27628317 | ||||||
chr16:27628469
|
G | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.141-192G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27628469 | ||||||
chr16:27628506
|
C | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.141-155C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 3/27 | chr16 | 27628506 | ||||||
chr16:27628938
|
C | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.310+108C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 4/27 | chr16 | 27628938 | ||||||
chr16:27629100
|
G | A | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+270G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 4/27 | chr16 | 27629100 | ||||||
chr16:27629165
|
C | CA | 13 | a0001c0001t0004g0081a0001c0005t0002g0147a0001c0008t0004g0026others(10): Show | 13 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.310+354dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr16 | 27629165 | |||||
chr16:27629177
|
A | G | 1 | a0001c0001t0008g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.310+347A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 4/27 | chr16 | 27629177 | ||||||
chr16:27629531
|
T | C | 1 | a0002c0002t0003g0098 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.310+701T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 4/27 | chr16 | 27629531 | ||||||
chr16:27629601
|
G | A | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.310+771G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 4/27 | chr16 | 27629601 | ||||||
chr16:27629657
|
C | T | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.310+827C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 4/27 | chr16 | 27629657 | ||||||
chr16:27629877
|
G | A | 1 | a0003c0003t0002g0128 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.310+1047G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 4/27 | chr16 | 27629877 | ||||||
chr16:27630366
|
A | G | 1 | a0001c0001t0008g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.311-699A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 4/27 | chr16 | 27630366 | ||||||
chr16:27630463
|
G | A | 6 | a0005c0006t0001g0013a0005c0006t0001g0058a0005c0006t0001g0059others(3): Show | 6 | HG00741.hp2 HG01243.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-602G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 4/27 | chr16 | 27630463 | ||||||
chr16:27630561
|
A | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.311-504A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 4/27 | chr16 | 27630561 | ||||||
chr16:27630582
|
G | C | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.311-483G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 4/27 | chr16 | 27630582 | ||||||
chr16:27630670
|
C | CTTCA | 7 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.311-374_311-371dup others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr16 | 27630670 | |||||
chr16:27630817
|
C | T | 4 | a0001c0004t0001g0132a0002c0002t0003g0134a0002c0002t0003g0135others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.311-248C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 4/27 | chr16 | 27630817 | ||||||
chr16:27630928
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.311-137A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 4/27 | chr16 | 27630928 | ||||||
chr16:27631315
|
G | A | 1 | a0003c0003t0002g0121 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.408+153G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27631315 | ||||||
chr16:27631543
|
T | TA | 10 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0083others(7): Show | 10 | HG00408.hp1 HG01978.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.408+398dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27631543 | |||||
chr16:27631543
|
TA | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.408+398delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27631543 | |||||
chr16:27632068
|
G | A | 2 | a0003c0003t0002g0126a0003c0003t0002g0129 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.408+906G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27632068 | ||||||
chr16:27632460
|
C | T | 1 | a0001c0001t0001g0021 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.408+1298C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27632460 | ||||||
chr16:27632475
|
C | T | 1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.408+1313C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27632475 | ||||||
chr16:27632619
|
C | T | 1 | a0001c0026t0004g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.408+1457C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27632619 | ||||||
chr16:27632752
|
T | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.408+1590T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27632752 | ||||||
chr16:27633206
|
C | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.408+2044C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27633206 | ||||||
chr16:27633455
|
A | T | 1 | a0004c0034t0005g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.408+2293A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27633455 | ||||||
chr16:27633457
|
A | AT | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.408+2301dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27633457 | |||||
chr16:27633539
|
G | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.408+2377G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27633539 | ||||||
chr16:27633662
|
A | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.408+2500A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27633662 | ||||||
chr16:27633746
|
G | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.408+2584G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27633746 | ||||||
chr16:27633817
|
G | C | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.408+2655G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27633817 | ||||||
chr16:27633863
|
A | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.408+2701A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27633863 | ||||||
chr16:27633912
|
G | A | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.408+2750G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27633912 | ||||||
chr16:27633917
|
G | C | 1 | a0001c0001t0001g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.408+2755G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27633917 | ||||||
chr16:27634357
|
G | A | 1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.408+3195G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27634357 | ||||||
chr16:27634813
|
C | T | 3 | a0007c0010t0002g0112a0007c0010t0002g0113a0007c0010t0002g0114 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.408+3651C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27634813 | ||||||
chr16:27634860
|
A | G | 1 | a0001c0026t0004g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.408+3698A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27634860 | ||||||
chr16:27634943
|
T | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.408+3781T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27634943 | ||||||
chr16:27635033
|
T | C | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+3871T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27635033 | ||||||
chr16:27636068
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.408+4906C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27636068 | ||||||
chr16:27636149
|
A | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.408+4987A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27636149 | ||||||
chr16:27636150
|
T | C | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.408+4988T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27636150 | ||||||
chr16:27636394
|
G | A | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.408+5232G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27636394 | ||||||
chr16:27636509
|
C | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.408+5347C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27636509 | ||||||
chr16:27636960
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.408+5798T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27636960 | ||||||
chr16:27637021
|
C | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.408+5859C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27637021 | ||||||
chr16:27637192
|
G | A | 16 | a0001c0024t0001g0078a0002c0002t0003g0062a0002c0002t0003g0063others(13): Show | 16 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.408+6030G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27637192 | ||||||
chr16:27637258
|
C | T | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.408+6096C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27637258 | ||||||
chr16:27637305
|
A | T | 19 | a0001c0012t0002g0137a0001c0012t0002g0143a0001c0024t0001g0078others(16): Show | 19 | HG00408.hp1 HG02074.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.408+6143A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27637305 | ||||||
chr16:27637504
|
C | T | 1 | a0001c0026t0004g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.408+6342C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27637504 | ||||||
chr16:27637674
|
G | A | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.408+6512G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27637674 | ||||||
chr16:27637869
|
C | T | 16 | a0001c0024t0001g0078a0002c0002t0003g0062a0002c0002t0003g0063others(13): Show | 16 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.408+6707C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27637869 | ||||||
chr16:27637997
|
C | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.408+6835C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27637997 | ||||||
chr16:27638013
|
C | T | 1 | a0017c0021t0001g0016 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.408+6851C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27638013 | ||||||
chr16:27638197
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.408+7035C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27638197 | ||||||
chr16:27638286
|
G | C | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.408+7124G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27638286 | ||||||
chr16:27638343
|
A | T | 1 | a0001c0001t0001g0093 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.408+7181A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27638343 | ||||||
chr16:27638672
|
C | T | 1 | a0001c0001t0004g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.408+7510C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27638672 | ||||||
chr16:27638835
|
A | AT | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.408+7694dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27638835 | |||||
chr16:27638835
|
A | ATT | 6 | a0001c0001t0002g0014a0001c0001t0009g0055a0001c0026t0004g0032others(3): Show | 6 | HG02622.hp2 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.408+7693_408+7694d others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27638835 | |||||
chr16:27638835
|
A | ATTT | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(2): Show | 5 | HG02970.hp1 HG03139.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.408+7692_408+7694d others(5): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27638835 | |||||
chr16:27638835
|
A | ATTTT | 16 | a0001c0005t0002g0149a0004c0007t0001g0074a0004c0007t0001g0075others(13): Show | 16 | HG02145.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.408+7691_408+7694d others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27638835 | |||||
chr16:27638979
|
ACT | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG00408.hp2 HG01978.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.408+7822_408+7823d others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27638979 | |||||
chr16:27639239
|
A | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.408+8077A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27639239 | ||||||
chr16:27639268
|
G | A | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.408+8106G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27639268 | ||||||
chr16:27639355
|
C | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.408+8193C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27639355 | ||||||
chr16:27639421
|
C | T | 1 | a0001c0001t0004g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.408+8259C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27639421 | ||||||
chr16:27639675
|
G | A | 1 | a0003c0003t0002g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.408+8513G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27639675 | ||||||
chr16:27639817
|
G | A | 1 | a0001c0004t0001g0042 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.408+8655G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27639817 | ||||||
chr16:27639915
|
GACCT | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-8684_409-8681d others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27639915 | |||||
chr16:27640208
|
C | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.409-8396C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27640208 | ||||||
chr16:27640677
|
AT | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(116): Show | 119 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.409-7909delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27640677 | |||||
chr16:27640849
|
A | C | 1 | a0001c0001t0004g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.409-7755A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27640849 | ||||||
chr16:27640862
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.409-7742G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27640862 | ||||||
chr16:27640876
|
A | C | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(121): Show | 124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.409-7728A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27640876 | ||||||
chr16:27640902
|
G | A | 1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.409-7702G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27640902 | ||||||
chr16:27640918
|
C | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-7686C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27640918 | ||||||
chr16:27641060
|
C | T | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.409-7544C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27641060 | ||||||
chr16:27641137
|
C | CA | 7 | a0001c0001t0001g0022a0001c0001t0004g0056a0001c0015t0001g0012others(4): Show | 7 | HG01258.hp1 HG01978.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.409-7453dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27641137 | |||||
chr16:27641137
|
CA | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-7453delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27641137 | |||||
chr16:27641152
|
G | A | 1 | a0002c0002t0003g0063 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.409-7452G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27641152 | ||||||
chr16:27641242
|
G | A | 1 | a0001c0026t0004g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.409-7362G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27641242 | ||||||
chr16:27641409
|
C | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-7195C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27641409 | ||||||
chr16:27641955
|
G | A | 1 | a0001c0001t0004g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.409-6649G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27641955 | ||||||
chr16:27642471
|
A | G | 2 | a0007c0010t0002g0112a0007c0010t0002g0113 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.409-6133A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27642471 | ||||||
chr16:27642520
|
AC | A | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-6082delC | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27642520 | |||||
chr16:27642536
|
G | C | 9 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(6): Show | 9 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.409-6068G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27642536 | ||||||
chr16:27642570
|
C | T | 1 | a0005c0006t0001g0085 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.409-6034C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27642570 | ||||||
chr16:27642576
|
G | C | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-6028G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27642576 | ||||||
chr16:27642654
|
C | T | 10 | a0001c0001t0001g0019a0001c0015t0001g0012a0001c0015t0001g0084others(7): Show | 10 | HG00741.hp2 HG01243.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.409-5950C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27642654 | ||||||
chr16:27642695
|
A | G | 1 | a0001c0001t0001g0038 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.409-5909A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27642695 | ||||||
chr16:27642726
|
T | A | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(123): Show | 126 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.409-5878T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27642726 | ||||||
chr16:27642739
|
C | G | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.409-5865C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27642739 | ||||||
chr16:27642762
|
T | TA | 16 | a0001c0024t0001g0078a0002c0002t0003g0062a0002c0002t0003g0063others(13): Show | 16 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.409-5842_409-5841i others(3): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27642762 | ||||||
chr16:27642763
|
T | A | 17 | a0001c0024t0001g0078a0002c0002t0003g0062a0002c0002t0003g0063others(14): Show | 17 | HG00408.hp1 HG01243.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.409-5841T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27642763 | ||||||
chr16:27642768
|
A | T | 1 | a0003c0003t0002g0130 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.409-5836A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27642768 | ||||||
chr16:27642769
|
A | T | 4 | a0003c0003t0002g0123a0003c0003t0002g0130a0003c0003t0002g0131others(1): Show | 4 | HG01243.hp1 HG01258.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-5835A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27642769 | ||||||
chr16:27642769
|
AT | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.409-5816delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27642769 | |||||
chr16:27642770
|
T | A | 42 | a0001c0001t0002g0071a0001c0004t0001g0116a0001c0004t0001g0117others(39): Show | 42 | HG01106.hp1 HG01109.hp2 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.409-5834T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27642770 | ||||||
chr16:27642849
|
C | A | 1 | a0007c0010t0002g0113 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.409-5755C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27642849 | ||||||
chr16:27642899
|
C | T | 1 | a0001c0015t0001g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.409-5705C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27642899 | ||||||
chr16:27642935
|
C | T | 1 | a0001c0015t0001g0084 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.409-5669C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27642935 | ||||||
chr16:27643100
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.409-5504A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27643100 | ||||||
chr16:27643214
|
G | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.409-5390G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27643214 | ||||||
chr16:27643259
|
A | G | 2 | a0001c0004t0001g0116a0001c0004t0001g0118 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.409-5345A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27643259 | ||||||
chr16:27643309
|
G | A | 1 | a0006c0009t0001g0096 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.409-5295G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27643309 | ||||||
chr16:27643445
|
T | C | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.409-5159T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27643445 | ||||||
chr16:27643550
|
C | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.409-5054C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27643550 | ||||||
chr16:27643590
|
C | CA | 22 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0015others(19): Show | 22 | HG00408.hp2 HG01106.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.409-4987dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27643590 | |||||
chr16:27643590
|
C | CAA | 45 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0019others(42): Show | 45 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.409-4988_409-4987d others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27643590 | |||||
chr16:27643590
|
C | CAAA | 40 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(37): Show | 40 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.409-4989_409-4987d others(5): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27643590 | |||||
chr16:27643590
|
C | CAAAA | 9 | a0001c0001t0002g0014a0002c0002t0003g0062a0002c0002t0003g0065others(6): Show | 9 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.409-4990_409-4987d others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27643590 | |||||
chr16:27643590
|
CA | C | 14 | a0001c0028t0004g0109a0003c0003t0002g0129a0004c0007t0001g0074others(11): Show | 14 | HG01515.hp1 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.409-4987delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27643590 | |||||
chr16:27643673
|
C | T | 1 | a0001c0001t0002g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.409-4931C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27643673 | ||||||
chr16:27643850
|
A | T | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.409-4754A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27643850 | ||||||
chr16:27644019
|
CT | C | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.409-4564delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27644019 | |||||
chr16:27644056
|
C | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.409-4548C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27644056 | ||||||
chr16:27644123
|
G | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.409-4481G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27644123 | ||||||
chr16:27644137
|
T | G | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.409-4467T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27644137 | ||||||
chr16:27644290
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.409-4314G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27644290 | ||||||
chr16:27644391
|
C | T | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.409-4213C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27644391 | ||||||
chr16:27644392
|
G | A | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.409-4212G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27644392 | ||||||
chr16:27644463
|
C | T | 3 | a0002c0002t0003g0072a0002c0002t0003g0099a0002c0002t0003g0102 | 3 | NA18962.hp1 NA18971.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.409-4141C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27644463 | ||||||
chr16:27644527
|
C | A | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(123): Show | 126 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.409-4077C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27644527 | ||||||
chr16:27644648
|
G | A | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.409-3956G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27644648 | ||||||
chr16:27644760
|
C | A | 1 | a0007c0010t0002g0113 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.409-3844C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27644760 | ||||||
chr16:27645015
|
G | A | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-3589G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27645015 | ||||||
chr16:27645168
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.409-3436C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27645168 | ||||||
chr16:27645209
|
G | A | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.409-3395G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27645209 | ||||||
chr16:27645230
|
T | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-3374T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27645230 | ||||||
chr16:27645320
|
G | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(133): Show | 136 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.409-3284G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27645320 | ||||||
chr16:27645438
|
G | A | 1 | a0001c0001t0004g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.409-3166G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27645438 | ||||||
chr16:27645447
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0092 | 2 | HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.409-3157C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27645447 | ||||||
chr16:27645489
|
C | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-3115C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27645489 | ||||||
chr16:27645525
|
G | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-3079G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27645525 | ||||||
chr16:27645561
|
A | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-3043A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27645561 | ||||||
chr16:27645919
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.409-2685G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27645919 | ||||||
chr16:27646018
|
C | T | 1 | a0005c0006t0001g0058 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.409-2586C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27646018 | ||||||
chr16:27646115
|
C | G | 1 | a0002c0002t0003g0072 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.409-2489C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27646115 | ||||||
chr16:27646522
|
G | T | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.409-2082G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27646522 | ||||||
chr16:27646633
|
G | A | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.409-1971G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27646633 | ||||||
chr16:27646657
|
G | A | 1 | a0001c0001t0008g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.409-1947G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27646657 | ||||||
chr16:27646757
|
AG | A | 9 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(6): Show | 9 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.409-1846delG | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27646757 | ||||||
chr16:27646796
|
A | G | 12 | a0001c0024t0001g0078a0002c0002t0003g0062a0002c0002t0003g0063others(9): Show | 12 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.409-1808A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27646796 | ||||||
chr16:27646874
|
T | G | 1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.409-1730T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27646874 | ||||||
chr16:27646890
|
C | T | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.409-1714C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27646890 | ||||||
chr16:27646930
|
G | A | 3 | a0006c0009t0001g0035a0006c0009t0001g0036a0006c0009t0001g0096 | 3 | HG01261.hp1 HG01361.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.409-1674G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27646930 | ||||||
chr16:27647240
|
C | A | 16 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0020others(13): Show | 16 | HG00408.hp2 HG01106.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.409-1364C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27647240 | ||||||
chr16:27647241
|
C | A | 16 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0020others(13): Show | 16 | HG00408.hp2 HG01106.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.409-1363C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27647241 | ||||||
chr16:27647338
|
GC | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-1258delC | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27647338 | |||||
chr16:27647392
|
A | G | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.409-1212A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27647392 | ||||||
chr16:27647508
|
A | AT | 117 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(114): Show | 117 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.409-1081dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27647508 | |||||
chr16:27647508
|
A | ATT | 16 | a0001c0024t0001g0078a0002c0002t0003g0062a0002c0002t0003g0063others(13): Show | 16 | HG00408.hp1 HG02074.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.409-1082_409-1081d others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27647508 | |||||
chr16:27647575
|
G | A | 4 | a0001c0001t0002g0011a0001c0001t0002g0034a0001c0001t0002g0040others(1): Show | 4 | HG02258.hp2 HG02280.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-1029G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27647575 | ||||||
chr16:27647598
|
C | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-1006C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27647598 | ||||||
chr16:27647611
|
T | C | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.409-993T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27647611 | ||||||
chr16:27647953
|
C | CA | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-649dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27647953 | |||||
chr16:27648059
|
A | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-545A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27648059 | ||||||
chr16:27648069
|
T | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-535T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27648069 | ||||||
chr16:27648292
|
C | CA | 14 | a0001c0024t0001g0078a0002c0002t0003g0062a0002c0002t0003g0065others(11): Show | 14 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.409-297dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr16 | 27648292 | |||||
chr16:27648351
|
G | A | 1 | a0003c0003t0002g0121 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.409-253G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27648351 | ||||||
chr16:27648425
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.409-179G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 5/27 | chr16 | 27648425 | ||||||
chr16:27648761
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.540+26C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27648761 | ||||||
chr16:27648931
|
G | A | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.540+196G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27648931 | ||||||
chr16:27648957
|
G | T | 1 | a0002c0002t0003g0068 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.540+222G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27648957 | ||||||
chr16:27649032
|
C | T | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+297C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27649032 | ||||||
chr16:27649217
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.540+482C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27649217 | ||||||
chr16:27649267
|
G | T | 1 | a0003c0003t0002g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.540+532G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27649267 | ||||||
chr16:27649547
|
T | C | 1 | a0001c0001t0008g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.540+812T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27649547 | ||||||
chr16:27650061
|
T | A | 4 | a0001c0004t0001g0132a0002c0002t0003g0134a0002c0002t0003g0135others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+1326T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27650061 | ||||||
chr16:27650171
|
T | TA | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.540+1447dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27650171 | |||||
chr16:27650260
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.540+1525G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27650260 | ||||||
chr16:27650556
|
C | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.540+1821C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27650556 | ||||||
chr16:27650559
|
C | T | 1 | a0003c0003t0002g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.540+1824C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27650559 | ||||||
chr16:27651107
|
C | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0092 | 3 | HG02056.hp2 HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.540+2372C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27651107 | ||||||
chr16:27651364
|
G | A | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.540+2629G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27651364 | ||||||
chr16:27651524
|
C | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.540+2789C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27651524 | ||||||
chr16:27651594
|
G | A | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+2859G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27651594 | ||||||
chr16:27651664
|
A | C | 1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.540+2929A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27651664 | ||||||
chr16:27651823
|
G | A | 1 | a0003c0003t0002g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.540+3088G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27651823 | ||||||
chr16:27652025
|
T | C | 4 | a0001c0004t0001g0132a0002c0002t0003g0134a0002c0002t0003g0135others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+3290T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27652025 | ||||||
chr16:27652378
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.540+3643G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27652378 | ||||||
chr16:27652388
|
C | T | 4 | a0001c0004t0001g0132a0002c0002t0003g0134a0002c0002t0003g0135others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+3653C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27652388 | ||||||
chr16:27652805
|
CA | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.540+4087delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27652805 | |||||
chr16:27653119
|
G | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.540+4384G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27653119 | ||||||
chr16:27653264
|
A | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(120): Show | 123 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.540+4529A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27653264 | ||||||
chr16:27653445
|
C | T | 1 | a0009c0014t0001g0018 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.540+4710C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27653445 | ||||||
chr16:27653576
|
G | T | 1 | a0015c0020t0004g0008 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.540+4841G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27653576 | ||||||
chr16:27653577
|
A | T | 1 | a0015c0020t0004g0008 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.540+4842A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27653577 | ||||||
chr16:27653578
|
G | T | 1 | a0015c0020t0004g0008 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.540+4843G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27653578 | ||||||
chr16:27653579
|
T | A | 1 | a0015c0020t0004g0008 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.540+4844T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27653579 | ||||||
chr16:27653580
|
G | A | 1 | a0015c0020t0004g0008 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.540+4845G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27653580 | ||||||
chr16:27653581
|
G | C | 1 | a0015c0020t0004g0008 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.540+4846G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27653581 | ||||||
chr16:27653582
|
G | A | 1 | a0015c0020t0004g0008 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.540+4847G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27653582 | ||||||
chr16:27653656
|
CT | C | 12 | a0003c0003t0002g0121a0004c0007t0001g0074a0004c0007t0001g0075others(9): Show | 12 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.540+4935delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27653656 | |||||
chr16:27654222
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.540+5487C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27654222 | ||||||
chr16:27654255
|
T | C | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.540+5520T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27654255 | ||||||
chr16:27654345
|
A | G | 4 | a0001c0004t0001g0132a0002c0002t0003g0134a0002c0002t0003g0135others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+5610A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27654345 | ||||||
chr16:27654411
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.540+5676G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27654411 | ||||||
chr16:27654426
|
A | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.540+5691A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27654426 | ||||||
chr16:27654515
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.540+5780G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27654515 | ||||||
chr16:27654770
|
G | A | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+6035G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27654770 | ||||||
chr16:27654823
|
C | T | 9 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.540+6088C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27654823 | ||||||
chr16:27654883
|
A | G | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.540+6148A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27654883 | ||||||
chr16:27654962
|
A | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.540+6227A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27654962 | ||||||
chr16:27654986
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.540+6251G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27654986 | ||||||
chr16:27655050
|
G | A | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.540+6315G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655050 | ||||||
chr16:27655158
|
G | A | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.540+6423G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655158 | ||||||
chr16:27655177
|
GAT | G | 13 | a0001c0001t0001g0047a0001c0001t0001g0087a0001c0001t0001g0092others(10): Show | 13 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.540+6493_540+6494d others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27655177 | |||||
chr16:27655177
|
GATAT | G | 12 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0095others(9): Show | 12 | HG00140.hp1 HG01243.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.540+6491_540+6494d others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27655177 | |||||
chr16:27655177
|
GATATAT | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(26): Show | 29 | HG00140.hp2 HG00408.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.540+6489_540+6494d others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27655177 | |||||
chr16:27655177
|
GATATATA others(1): Show |
G | 20 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0038others(17): Show | 20 | HG00099.hp1 HG01106.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.540+6487_540+6494d others(10): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27655177 | |||||
chr16:27655177
|
GATATATA others(3): Show |
G | 15 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0093others(12): Show | 15 | HG00741.hp1 HG01361.hp2 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.540+6485_540+6494d others(12): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27655177 | |||||
chr16:27655177
|
GATATATA others(5): Show |
G | 7 | a0001c0001t0001g0028a0001c0001t0002g0046a0001c0015t0001g0084others(4): Show | 7 | HG01258.hp2 HG01361.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+6483_540+6494d others(14): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27655177 | |||||
chr16:27655177
|
GATATATA others(7): Show |
G | 3 | a0001c0005t0001g0144a0001c0005t0001g0145a0007c0010t0002g0114 | 3 | HG02970.hp1 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.540+6481_540+6494d others(16): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27655177 | |||||
chr16:27655177
|
GATATATA others(9): Show |
G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.540+6479_540+6494d others(18): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27655177 | |||||
chr16:27655177
|
GATATATA others(11): Show |
G | 2 | a0001c0004t0002g0070a0001c0004t0002g0073 | 2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.540+6477_540+6494d others(20): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27655177 | |||||
chr16:27655177
|
GATATATA others(13): Show |
G | 4 | a0001c0001t0002g0071a0001c0028t0004g0109a0005c0006t0001g0013others(1): Show | 4 | HG02056.hp1 HG02109.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+6475_540+6494d others(22): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27655177 | |||||
chr16:27655177
|
GATATATA others(15): Show |
G | 1 | a0001c0004t0002g0069 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.540+6473_540+6494d others(24): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27655177 | |||||
chr16:27655177
|
GATATATA others(17): Show |
G | 10 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(7): Show | 10 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.540+6471_540+6494d others(26): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27655177 | |||||
chr16:27655177
|
GATATATA others(19): Show |
G | 16 | a0001c0004t0001g0132a0001c0012t0002g0137a0001c0012t0002g0143others(13): Show | 16 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.540+6469_540+6494d others(28): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27655177 | |||||
chr16:27655177
|
GATATATA others(21): Show |
G | 2 | a0002c0029t0003g0101a0004c0007t0010g0108 | 2 | HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.540+6467_540+6494d others(30): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27655177 | |||||
chr16:27655177
|
GATATATA others(23): Show |
G | 12 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(9): Show | 12 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.540+6465_540+6494d others(32): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27655177 | |||||
chr16:27655182
|
A | G | 2 | a0001c0011t0002g0141a0001c0011t0002g0152 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.540+6447A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655182 | ||||||
chr16:27655183
|
T | G | 4 | a0001c0011t0002g0141a0001c0011t0002g0152a0007c0010t0002g0112others(1): Show | 4 | HG01243.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+6448T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655183 | ||||||
chr16:27655184
|
A | G | 1 | a0012c0033t0002g0142 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.540+6449A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655184 | ||||||
chr16:27655185
|
T | G | 1 | a0012c0033t0002g0142 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.540+6450T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655185 | ||||||
chr16:27655204
|
A | G | 1 | a0005c0006t0001g0085 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.540+6469A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655204 | ||||||
chr16:27655216
|
A | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.540+6481A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655216 | ||||||
chr16:27655218
|
A | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.540+6483A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655218 | ||||||
chr16:27655220
|
A | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.540+6485A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655220 | ||||||
chr16:27655222
|
A | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.540+6487A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655222 | ||||||
chr16:27655224
|
A | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.540+6489A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655224 | ||||||
chr16:27655226
|
A | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.540+6491A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655226 | ||||||
chr16:27655228
|
A | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.540+6493A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655228 | ||||||
chr16:27655229
|
T | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.540+6494T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655229 | ||||||
chr16:27655365
|
C | T | 1 | a0013c0027t0001g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.540+6630C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655365 | ||||||
chr16:27655400
|
A | ATTATTTA others(1): Show |
4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+6688_540+6695d others(10): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27655400 | |||||
chr16:27655400
|
A | ATTATTTA others(9): Show |
9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.540+6680_540+6695d others(18): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27655400 | |||||
chr16:27655603
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.540+6868T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655603 | ||||||
chr16:27655855
|
T | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.540+7120T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27655855 | ||||||
chr16:27656054
|
G | A | 5 | a0001c0011t0002g0141a0001c0011t0002g0152a0001c0028t0004g0109others(2): Show | 5 | HG01243.hp2 HG02280.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+7319G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27656054 | ||||||
chr16:27656419
|
G | GA | 11 | a0001c0001t0001g0093a0001c0001t0004g0056a0001c0001t0006g0037others(8): Show | 11 | HG00741.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.540+7705dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27656419 | |||||
chr16:27656419
|
G | GAA | 7 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(4): Show | 7 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+7704_540+7705d others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27656419 | |||||
chr16:27656502
|
A | G | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.540+7767A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27656502 | ||||||
chr16:27656603
|
G | A | 10 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(7): Show | 10 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.540+7868G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27656603 | ||||||
chr16:27656617
|
T | C | 1 | a0004c0034t0005g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.540+7882T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27656617 | ||||||
chr16:27656884
|
A | G | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.540+8149A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27656884 | ||||||
chr16:27656934
|
TA | T | 14 | a0001c0001t0001g0093a0001c0008t0004g0079a0001c0012t0002g0137others(11): Show | 14 | HG00741.hp1 HG00741.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.540+8212delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27656934 | |||||
chr16:27656951
|
T | TA | 23 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(20): Show | 23 | HG00408.hp1 HG01109.hp2 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.540+8225dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27656951 | |||||
chr16:27657616
|
C | CA | 10 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(7): Show | 10 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.540+8891dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27657616 | |||||
chr16:27657705
|
T | G | 1 | a0004c0007t0001g0074 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.540+8970T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27657705 | ||||||
chr16:27657771
|
G | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.540+9036G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27657771 | ||||||
chr16:27657934
|
A | G | 2 | a0001c0001t0001g0053a0009c0014t0001g0043 | 2 | HG01258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.540+9199A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27657934 | ||||||
chr16:27657967
|
G | C | 1 | a0001c0004t0002g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.540+9232G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27657967 | ||||||
chr16:27658184
|
C | T | 1 | a0001c0015t0001g0084 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.540+9449C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27658184 | ||||||
chr16:27658291
|
A | G | 4 | a0001c0001t0002g0014a0001c0001t0002g0033a0001c0001t0002g0046others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+9556A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27658291 | ||||||
chr16:27658302
|
A | T | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.540+9567A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27658302 | ||||||
chr16:27658670
|
C | T | 1 | a0001c0001t0008g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.540+9935C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27658670 | ||||||
chr16:27658717
|
C | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.540+9982C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27658717 | ||||||
chr16:27658718
|
C | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0092 | 3 | HG02056.hp2 HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.540+9983C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27658718 | ||||||
chr16:27658755
|
T | G | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.540+10020T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27658755 | ||||||
chr16:27658793
|
G | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(134): Show | 137 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.540+10058G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27658793 | ||||||
chr16:27658793
|
G | T | 1 | a0001c0001t0002g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.540+10058G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27658793 | ||||||
chr16:27658901
|
T | G | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.540+10166T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27658901 | ||||||
chr16:27658914
|
T | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(135): Show | 138 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.540+10179T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27658914 | ||||||
chr16:27658943
|
T | C | 16 | a0001c0024t0001g0078a0002c0002t0003g0062a0002c0002t0003g0063others(13): Show | 16 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.540+10208T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27658943 | ||||||
chr16:27659104
|
A | G | 1 | a0001c0004t0001g0042 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.540+10369A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27659104 | ||||||
chr16:27659171
|
C | A | 1 | a0009c0014t0001g0043 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.540+10436C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27659171 | ||||||
chr16:27659423
|
T | C | 1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.540+10688T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27659423 | ||||||
chr16:27659438
|
A | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.540+10703A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27659438 | ||||||
chr16:27659465
|
G | A | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.540+10730G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27659465 | ||||||
chr16:27659512
|
CA | C | 20 | a0001c0001t0004g0025a0001c0012t0002g0137a0001c0012t0002g0143others(17): Show | 20 | HG00408.hp1 HG02074.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.540+10791delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27659512 | |||||
chr16:27659798
|
G | A | 1 | a0001c0001t0004g0056 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.540+11063G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27659798 | ||||||
chr16:27660002
|
C | T | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.540+11267C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27660002 | ||||||
chr16:27660209
|
C | T | 1 | a0001c0011t0002g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.540+11474C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27660209 | ||||||
chr16:27660403
|
A | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.540+11668A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27660403 | ||||||
chr16:27660412
|
G | T | 1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.540+11677G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27660412 | ||||||
chr16:27660636
|
C | CT | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.540+11917dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27660636 | |||||
chr16:27660772
|
G | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(135): Show | 138 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.540+12037G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27660772 | ||||||
chr16:27660784
|
C | A | 4 | a0001c0004t0001g0132a0002c0002t0003g0134a0002c0002t0003g0135others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+12049C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27660784 | ||||||
chr16:27660790
|
C | T | 2 | a0001c0028t0004g0109a0018c0025t0003g0111 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.540+12055C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27660790 | ||||||
chr16:27660797
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | NA18747.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.540+12062A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27660797 | ||||||
chr16:27661100
|
G | A | 26 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(23): Show | 26 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.540+12365G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661100 | ||||||
chr16:27661104
|
A | C | 23 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(20): Show | 23 | HG00408.hp1 HG01109.hp2 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.540+12369A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661104 | ||||||
chr16:27661377
|
T | C | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.540+12642T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661377 | ||||||
chr16:27661477
|
C | T | 1 | a0001c0001t0004g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.540+12742C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661477 | ||||||
chr16:27661490
|
A | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.540+12755A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661490 | ||||||
chr16:27661542
|
C | T | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+12807C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661542 | ||||||
chr16:27661581
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0082a0001c0001t0001g0089 | 3 | HG02155.hp1 HG02155.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.540+12846G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661581 | ||||||
chr16:27661806
|
C | T | 16 | a0001c0024t0001g0078a0002c0002t0003g0062a0002c0002t0003g0063others(13): Show | 16 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.540+13071C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661806 | ||||||
chr16:27661911
|
A | AAT | 7 | a0001c0001t0002g0034a0001c0001t0002g0040a0001c0001t0004g0005others(4): Show | 7 | HG02055.hp1 HG02145.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+13220_540+1322 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661911 | |||||
chr16:27661911
|
A | T | 2 | a0001c0011t0002g0152a0012c0033t0002g0142 | 2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.540+13176A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661911 | ||||||
chr16:27661911
|
AAT | A | 17 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0038others(14): Show | 17 | HG00741.hp2 HG01106.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.540+13220_540+1322 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661911 | |||||
chr16:27661911
|
AATAT | A | 15 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0021others(12): Show | 15 | HG00099.hp2 HG02109.hp1 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.540+13218_540+1322 others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661911 | |||||
chr16:27661911
|
AATATAT | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0028 | 3 | HG01978.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.540+13216_540+1322 others(10): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661911 | |||||
chr16:27661911
|
AATATATA others(1): Show |
A | 3 | a0001c0001t0001g0019a0003c0003t0001g0127a0013c0027t0001g0004 | 3 | HG01261.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.540+13214_540+1322 others(12): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661911 | |||||
chr16:27661911
|
AATATATA others(3): Show |
A | 8 | a0003c0003t0002g0120a0003c0003t0002g0125a0003c0003t0002g0126others(5): Show | 8 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.540+13212_540+1322 others(14): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661911 | |||||
chr16:27661911
|
AATATATA others(5): Show |
A | 2 | a0001c0012t0002g0137a0018c0025t0003g0111 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.540+13210_540+1322 others(16): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661911 | |||||
chr16:27661911
|
AATATATA others(7): Show |
A | 1 | a0006c0009t0001g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.540+13208_540+1322 others(18): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661911 | |||||
chr16:27661911
|
AATATATA others(9): Show |
A | 2 | a0001c0001t0002g0088a0001c0001t0004g0017 | 2 | HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.540+13206_540+1322 others(20): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661911 | |||||
chr16:27661911
|
AATATATA others(45): Show |
A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | NA18747.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.540+13200_540+1325 others(56): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661911 | |||||
chr16:27661919
|
TATATATA others(37): Show |
T | 1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.540+13208_540+1325 others(48): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661919 | |||||
chr16:27661923
|
TATATATA others(33): Show |
T | 5 | a0001c0012t0002g0143a0002c0002t0003g0063a0002c0002t0003g0098others(2): Show | 5 | HG03139.hp1 NA18954.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+13212_540+1325 others(44): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661923 | |||||
chr16:27661925
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.540+13190T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661925 | ||||||
chr16:27661925
|
TATATATA others(31): Show |
T | 11 | a0001c0024t0001g0078a0002c0002t0003g0062a0002c0002t0003g0065others(8): Show | 11 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.540+13214_540+1325 others(42): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661925 | |||||
chr16:27661927
|
TATATATA others(29): Show |
T | 2 | a0001c0004t0001g0117a0001c0004t0001g0138 | 2 | HG01109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.540+13216_540+1325 others(40): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661927 | |||||
chr16:27661931
|
T | TATACACA others(3): Show |
1 | a0009c0014t0001g0043 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.540+13199_540+1320 others(14): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661931 | |||||
chr16:27661931
|
TATATATA others(25): Show |
T | 2 | a0001c0004t0001g0116a0001c0004t0001g0118 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.540+13220_540+1325 others(36): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661931 | |||||
chr16:27661933
|
T | TATATATA others(9): Show |
1 | a0001c0001t0001g0057 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.540+13207_540+1320 others(20): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661933 | |||||
chr16:27661933
|
TATATATA others(23): Show |
T | 2 | a0001c0004t0001g0132a0002c0002t0003g0134 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.540+13278_540+1330 others(34): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661933 | |||||
chr16:27661935
|
T | TATATATA others(15): Show |
2 | a0007c0010t0002g0112a0007c0010t0002g0113 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.540+13215_540+1321 others(26): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661935 | |||||
chr16:27661935
|
T | TATATATA others(19): Show |
1 | a0001c0001t0001g0002 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.540+13219_540+1322 others(30): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661935 | |||||
chr16:27661935
|
TATATATA others(135): Show |
T | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+13212_540+1335 others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661935 | |||||
chr16:27661937
|
T | TATATATA others(11): Show |
1 | a0003c0003t0002g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.540+13213_540+1321 others(22): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661937 | |||||
chr16:27661937
|
T | TATATATA others(13): Show |
1 | a0003c0003t0002g0121 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.540+13215_540+1321 others(24): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661937 | |||||
chr16:27661941
|
T | TATATACA others(5): Show |
4 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(1): Show | 4 | HG02970.hp1 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+13211_540+1321 others(16): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661941 | |||||
chr16:27661943
|
T | TATACACA others(3): Show |
3 | a0001c0005t0002g0148a0003c0003t0002g0123a0003c0003t0002g0139 | 3 | HG01358.hp2 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.540+13211_540+1321 others(14): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661943 | |||||
chr16:27661945
|
TATATATA others(37): Show |
T | 1 | a0002c0002t0003g0067 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.540+13214_540+1325 others(48): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661945 | |||||
chr16:27661947
|
T | TACACATA others(1): Show |
2 | a0001c0005t0002g0149a0007c0010t0002g0114 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.540+13213_540+1321 others(12): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661947 | |||||
chr16:27661947
|
TATATATA others(123): Show |
T | 4 | a0004c0007t0001g0075a0004c0007t0001g0105a0008c0016t0001g0077others(1): Show | 4 | HG02055.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+13222_540+1335 others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661947 | |||||
chr16:27661949
|
TATATATA others(121): Show |
T | 2 | a0004c0007t0001g0074a0019c0032t0003g0001 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.540+13222_540+1334 others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661949 | |||||
chr16:27661951
|
TATATACA others(31): Show |
T | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.540+13220_540+1325 others(42): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661951 | |||||
chr16:27661951
|
TATATACA others(119): Show |
T | 3 | a0004c0007t0010g0108a0004c0007t0012g0106a0008c0016t0001g0076 | 3 | HG02451.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.540+13222_540+1334 others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661951 | |||||
chr16:27661955
|
T | C | 8 | a0001c0001t0001g0083a0001c0001t0001g0095a0001c0001t0004g0081others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.540+13220T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661955 | ||||||
chr16:27661957
|
C | T | 17 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0083others(14): Show | 17 | HG01109.hp1 HG01358.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.540+13222C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661957 | ||||||
chr16:27661959
|
C | T | 13 | a0001c0001t0001g0047a0001c0001t0001g0095a0001c0001t0002g0071others(10): Show | 13 | HG01109.hp1 HG01358.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.540+13224C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661959 | ||||||
chr16:27661961
|
T | C | 7 | a0001c0001t0001g0054a0001c0001t0001g0095a0001c0001t0002g0011others(4): Show | 7 | HG01106.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+13226T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661961 | ||||||
chr16:27661963
|
C | CACAT | 3 | a0001c0001t0001g0047a0001c0001t0001g0083a0001c0001t0007g0091 | 3 | HG01109.hp1 HG02572.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.540+13229_540+1323 others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661963 | |||||
chr16:27661963
|
C | T | 9 | a0001c0001t0001g0054a0001c0001t0001g0095a0001c0001t0002g0011others(6): Show | 9 | HG02258.hp2 HG02717.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.540+13228C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661963 | ||||||
chr16:27661963
|
CAT | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(20): Show | 23 | HG00408.hp2 HG01106.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.540+13250_540+1325 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661963 | |||||
chr16:27661963
|
CATAT | C | 11 | a0001c0001t0001g0023a0001c0001t0001g0093a0003c0003t0001g0127others(8): Show | 11 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.540+13248_540+1325 others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661963 | |||||
chr16:27661965
|
T | C | 14 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0083others(11): Show | 14 | HG01109.hp1 HG01358.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.540+13230T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661965 | ||||||
chr16:27661965
|
TATATATA others(21): Show |
T | 2 | a0002c0002t0003g0135a0002c0002t0003g0136 | 2 | HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.540+13252_540+1327 others(32): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661965 | |||||
chr16:27661967
|
T | C | 2 | a0001c0001t0002g0071a0001c0018t0011g0122 | 2 | HG01106.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.540+13232T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661967 | ||||||
chr16:27661967
|
T | TACAC | 2 | a0001c0005t0002g0149a0007c0010t0002g0114 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.540+13233_540+1323 others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661967 | |||||
chr16:27661969
|
T | C | 2 | a0003c0003t0002g0123a0003c0003t0002g0139 | 2 | HG01358.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.540+13234T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661969 | ||||||
chr16:27661977
|
T | TAC | 2 | a0007c0010t0002g0112a0007c0010t0002g0113 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.540+13243_540+1324 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661977 | |||||
chr16:27661979
|
T | C | 2 | a0007c0010t0002g0112a0007c0010t0002g0113 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.540+13244T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661979 | ||||||
chr16:27661985
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.540+13250T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661985 | ||||||
chr16:27661987
|
C | T | 5 | a0001c0001t0001g0019a0003c0003t0002g0123a0003c0003t0002g0139others(2): Show | 5 | HG01358.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+13252C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661987 | ||||||
chr16:27661989
|
C | T | 4 | a0003c0003t0002g0123a0003c0003t0002g0139a0007c0010t0002g0112others(1): Show | 4 | HG01358.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+13254C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661989 | ||||||
chr16:27661991
|
T | C | 5 | a0001c0028t0004g0109a0002c0002t0003g0067a0002c0029t0003g0101others(2): Show | 5 | HG01358.hp2 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+13256T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661991 | ||||||
chr16:27661993
|
C | CAT | 7 | a0001c0001t0001g0039a0001c0001t0002g0014a0001c0012t0002g0143others(4): Show | 7 | HG01517.hp2 HG02818.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+13280_540+1328 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661993 | |||||
chr16:27661993
|
C | T | 7 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(4): Show | 7 | HG02970.hp1 HG03098.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+13258C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661993 | ||||||
chr16:27661993
|
CAT | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(23): Show | 26 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(23): Show |
intron_variant | MODIFIER | c.540+13280_540+1328 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661993 | |||||
chr16:27661993
|
CATAT | C | 15 | a0001c0001t0004g0051a0001c0001t0008g0050a0001c0015t0001g0012others(12): Show | 15 | HG00140.hp1 HG01258.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.540+13278_540+1328 others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661993 | |||||
chr16:27661993
|
CATATATA others(27): Show |
C | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.540+13274_540+1330 others(38): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661993 | |||||
chr16:27661995
|
T | C | 2 | a0007c0010t0002g0112a0007c0010t0002g0113 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.540+13260T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661995 | ||||||
chr16:27661995
|
T | TATATATA others(17): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0089 | 2 | HG02155.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.540+13277_540+1327 others(28): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661995 | |||||
chr16:27661995
|
T | TATATATA others(19): Show |
1 | a0001c0001t0001g0082 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.540+13279_540+1328 others(30): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661995 | |||||
chr16:27661997
|
T | C | 6 | a0001c0001t0001g0019a0001c0028t0004g0109a0002c0002t0003g0067others(3): Show | 6 | HG01358.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+13262T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27661997 | ||||||
chr16:27661997
|
T | TATATATA others(17): Show |
1 | a0001c0023t0001g0060 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.540+13279_540+1328 others(28): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661997 | |||||
chr16:27661999
|
T | TATACAC | 2 | a0001c0005t0002g0148a0001c0005t0002g0149 | 2 | HG03098.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.540+13267_540+1326 others(10): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661999 | |||||
chr16:27661999
|
TATATATA others(17): Show |
T | 1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.540+13282_540+1330 others(28): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27661999 | |||||
chr16:27662001
|
T | TACAC | 4 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(1): Show | 4 | HG02970.hp1 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+13267_540+1326 others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27662001 | |||||
chr16:27662011
|
T | C | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.540+13276T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662011 | ||||||
chr16:27662013
|
T | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0057a0001c0001t0001g0092others(5): Show | 8 | HG00140.hp2 HG01106.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.540+13278T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662013 | ||||||
chr16:27662015
|
T | C | 24 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(21): Show | 24 | HG00140.hp2 HG00408.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.540+13280T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662015 | ||||||
chr16:27662017
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0057a0001c0001t0004g0005others(3): Show | 6 | HG00140.hp2 HG01243.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+13282C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662017 | ||||||
chr16:27662019
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.540+13284C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662019 | ||||||
chr16:27662021
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.540+13286T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662021 | ||||||
chr16:27662023
|
C | CAT | 5 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0047others(2): Show | 5 | HG01109.hp1 HG02155.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+13306_540+1330 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27662023 | |||||
chr16:27662023
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0057a0001c0001t0001g0095others(5): Show | 8 | HG00140.hp2 HG01106.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.540+13288C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662023 | ||||||
chr16:27662023
|
CAT | C | 14 | a0001c0015t0001g0084a0002c0002t0003g0135a0003c0003t0001g0127others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.540+13306_540+1330 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27662023 | |||||
chr16:27662026
|
A | G | 1 | a0009c0014t0001g0043 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.540+13291A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662026 | ||||||
chr16:27662035
|
T | C | 4 | a0001c0001t0004g0005a0001c0011t0002g0141a0001c0011t0002g0152others(1): Show | 4 | HG01106.hp1 HG01243.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+13300T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662035 | ||||||
chr16:27662035
|
T | TACACAC | 3 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146 | 3 | HG02970.hp1 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.540+13301_540+1330 others(10): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27662035 | |||||
chr16:27662035
|
TATATATA others(7): Show |
T | 1 | a0009c0014t0001g0043 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.540+13308_540+1332 others(18): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27662035 | |||||
chr16:27662037
|
T | C | 15 | a0001c0001t0001g0057a0001c0001t0004g0005a0001c0001t0004g0049others(12): Show | 15 | HG00140.hp2 HG01106.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.540+13302T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662037 | ||||||
chr16:27662037
|
TATATACA others(5): Show |
T | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.540+13308_540+1331 others(16): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27662037 | |||||
chr16:27662039
|
T | C | 14 | a0001c0001t0001g0057a0001c0001t0004g0049a0001c0005t0002g0147others(11): Show | 14 | HG00140.hp2 HG01106.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.540+13304T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662039 | ||||||
chr16:27662039
|
T | TACAC | 2 | a0001c0001t0001g0010a0001c0001t0004g0056 | 2 | HG02145.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.540+13305_540+1330 others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27662039 | |||||
chr16:27662041
|
T | C | 46 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0039others(43): Show | 46 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.540+13306T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662041 | ||||||
chr16:27662043
|
C | CAT | 13 | a0001c0001t0001g0053a0001c0001t0004g0024a0001c0001t0004g0052others(10): Show | 13 | HG01109.hp2 HG02055.hp1 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.540+13309_540+1331 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27662043 | |||||
chr16:27662043
|
C | T | 4 | a0001c0001t0004g0005a0001c0005t0001g0144a0001c0005t0001g0145others(1): Show | 4 | HG02970.hp1 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+13308C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662043 | ||||||
chr16:27662045
|
C | T | 26 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0028others(23): Show | 26 | HG00140.hp2 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.540+13310C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662045 | ||||||
chr16:27662047
|
T | C | 15 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0004g0025others(12): Show | 15 | HG00741.hp2 HG01243.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.540+13312T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662047 | ||||||
chr16:27662049
|
C | CAT | 14 | a0001c0001t0001g0045a0001c0001t0002g0011a0001c0001t0002g0033others(11): Show | 14 | HG02258.hp2 HG02280.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.540+13336_540+1333 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27662049 | |||||
chr16:27662049
|
C | CATAT | 10 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0054others(7): Show | 10 | HG01361.hp2 HG01515.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.540+13334_540+1333 others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27662049 | |||||
chr16:27662049
|
C | CATATAT | 13 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0133others(10): Show | 13 | HG00099.hp2 HG01261.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.540+13332_540+1333 others(10): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27662049 | |||||
chr16:27662049
|
C | CATATATA others(1): Show |
4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(1): Show | 4 | HG01358.hp1 HG02155.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+13330_540+1333 others(12): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27662049 | |||||
chr16:27662049
|
C | CATATATA others(9): Show |
1 | a0001c0001t0001g0093 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.540+13322_540+1333 others(20): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27662049 | |||||
chr16:27662049
|
C | T | 39 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0028others(36): Show | 39 | HG00140.hp2 HG00741.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.540+13314C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662049 | ||||||
chr16:27662071
|
T | C | 7 | a0001c0004t0001g0132a0001c0018t0011g0122a0003c0003t0002g0125others(4): Show | 7 | HG01106.hp1 HG01258.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+13336T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662071 | ||||||
chr16:27662071
|
T | TAC | 18 | a0001c0011t0002g0141a0001c0011t0002g0152a0002c0002t0003g0134others(15): Show | 18 | HG00099.hp1 HG00140.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.540+13342_540+1334 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27662071 | |||||
chr16:27662095
|
C | CAT | 50 | a0001c0001t0001g0019a0001c0001t0002g0040a0001c0001t0002g0071others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.540+13378_540+1337 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27662095 | |||||
chr16:27662095
|
C | CATAT | 8 | a0001c0004t0001g0132a0001c0004t0002g0069a0001c0004t0002g0070others(5): Show | 8 | HG02630.hp1 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.540+13376_540+1337 others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27662095 | |||||
chr16:27662383
|
G | T | 3 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0052 | 3 | HG02055.hp1 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.540+13648G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27662383 | ||||||
chr16:27663152
|
C | CT | 47 | a0001c0001t0001g0031a0001c0001t0004g0005a0001c0005t0001g0144others(44): Show | 47 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.540+14441dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27663152 | |||||
chr16:27663152
|
CT | C | 19 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0004t0002g0069others(16): Show | 19 | HG02055.hp2 HG02132.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.540+14441delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27663152 | |||||
chr16:27663152
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.540+14431_540+1444 others(15): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27663152 | |||||
chr16:27663234
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0092 | 3 | HG02056.hp2 HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.541-14495G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27663234 | ||||||
chr16:27663473
|
T | C | 65 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(62): Show | 65 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.541-14256T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27663473 | ||||||
chr16:27664004
|
G | T | 11 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0052others(8): Show | 11 | HG01258.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.541-13725G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27664004 | ||||||
chr16:27664010
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.541-13719C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27664010 | ||||||
chr16:27664292
|
G | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0092 | 3 | HG02056.hp2 HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.541-13437G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27664292 | ||||||
chr16:27664462
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.541-13267C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27664462 | ||||||
chr16:27664583
|
C | G | 1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.541-13146C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27664583 | ||||||
chr16:27664702
|
A | G | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-13027A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27664702 | ||||||
chr16:27664848
|
T | G | 1 | a0001c0004t0002g0069 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.541-12881T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27664848 | ||||||
chr16:27665118
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.541-12611C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27665118 | ||||||
chr16:27665126
|
G | T | 2 | a0001c0004t0001g0116a0001c0004t0001g0118 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.541-12603G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27665126 | ||||||
chr16:27665244
|
T | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-12485T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27665244 | ||||||
chr16:27665286
|
G | A | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-12443G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27665286 | ||||||
chr16:27665606
|
AT | A | 12 | a0001c0004t0001g0132a0001c0008t0004g0079a0003c0003t0002g0129others(9): Show | 12 | HG01515.hp1 HG02055.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.541-12108delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27665606 | |||||
chr16:27665635
|
CTT | C | 2 | a0001c0012t0002g0137a0001c0012t0002g0143 | 2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.541-12092_541-1209 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27665635 | |||||
chr16:27665855
|
C | G | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-11874C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27665855 | ||||||
chr16:27665894
|
C | G | 1 | a0008c0016t0001g0076 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.541-11835C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27665894 | ||||||
chr16:27665904
|
C | G | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.541-11825C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27665904 | ||||||
chr16:27666175
|
T | G | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.541-11554T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27666175 | ||||||
chr16:27666392
|
T | TTTTTG | 29 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0020others(26): Show | 29 | HG00408.hp2 HG01106.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.541-11297_541-1129 others(9): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27666392 | |||||
chr16:27666392
|
T | TTTTTGTT others(3): Show |
4 | a0001c0001t0009g0055a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-11302_541-1129 others(14): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27666392 | |||||
chr16:27666392
|
TTTTTG | T | 16 | a0001c0001t0001g0019a0002c0029t0003g0101a0003c0003t0001g0127others(13): Show | 16 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.541-11297_541-1129 others(9): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27666392 | |||||
chr16:27666392
|
TTTTTGTT others(3): Show |
T | 2 | a0003c0003t0002g0123a0018c0025t0003g0111 | 2 | HG01358.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.541-11302_541-1129 others(14): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27666392 | |||||
chr16:27666560
|
G | C | 1 | a0001c0001t0001g0023 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.541-11169G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27666560 | ||||||
chr16:27666578
|
C | A | 1 | a0017c0021t0001g0016 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.541-11151C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27666578 | ||||||
chr16:27666619
|
T | C | 1 | a0003c0003t0002g0120 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.541-11110T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27666619 | ||||||
chr16:27666661
|
C | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-11068C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27666661 | ||||||
chr16:27666694
|
G | A | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.541-11035G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27666694 | ||||||
chr16:27666710
|
G | A | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.541-11019G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27666710 | ||||||
chr16:27666887
|
C | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.541-10842C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27666887 | ||||||
chr16:27666924
|
G | C | 19 | a0001c0012t0002g0137a0001c0012t0002g0143a0001c0024t0001g0078others(16): Show | 19 | HG00408.hp1 HG02074.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.541-10805G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27666924 | ||||||
chr16:27667092
|
A | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-10637A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27667092 | ||||||
chr16:27667100
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.541-10629C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27667100 | ||||||
chr16:27667248
|
G | A | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.541-10481G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27667248 | ||||||
chr16:27667296
|
T | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-10433T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27667296 | ||||||
chr16:27667419
|
G | A | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-10310G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27667419 | ||||||
chr16:27667582
|
G | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0092 | 3 | HG02056.hp2 HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.541-10147G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27667582 | ||||||
chr16:27667855
|
T | G | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.541-9874T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27667855 | ||||||
chr16:27667991
|
G | A | 23 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(20): Show | 23 | HG00408.hp1 HG01109.hp2 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.541-9738G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27667991 | ||||||
chr16:27668076
|
C | T | 1 | a0001c0015t0001g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.541-9653C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27668076 | ||||||
chr16:27668524
|
C | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0004g0005others(2): Show | 5 | HG01515.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-9205C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27668524 | ||||||
chr16:27668573
|
G | A | 1 | a0010c0013t0003g0061 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.541-9156G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27668573 | ||||||
chr16:27668603
|
C | G | 1 | a0012c0033t0002g0142 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.541-9126C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27668603 | ||||||
chr16:27668695
|
C | T | 3 | a0005c0006t0001g0058a0005c0006t0001g0059a0005c0006t0001g0064 | 3 | NA18971.hp2 NA19080.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.541-9034C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27668695 | ||||||
chr16:27668777
|
A | G | 41 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.541-8952A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27668777 | ||||||
chr16:27668784
|
T | C | 29 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.541-8945T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27668784 | ||||||
chr16:27668934
|
A | C | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.541-8795A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27668934 | ||||||
chr16:27669116
|
T | C | 19 | a0001c0012t0002g0137a0001c0012t0002g0143a0001c0024t0001g0078others(16): Show | 19 | HG00408.hp1 HG02074.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.541-8613T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27669116 | ||||||
chr16:27669361
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.541-8368G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27669361 | ||||||
chr16:27669577
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.541-8152G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27669577 | ||||||
chr16:27669668
|
T | C | 13 | a0003c0003t0001g0127a0003c0003t0002g0094a0003c0003t0002g0120others(10): Show | 13 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.541-8061T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27669668 | ||||||
chr16:27669824
|
G | C | 1 | a0009c0014t0001g0018 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.541-7905G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27669824 | ||||||
chr16:27669833
|
A | AT | 13 | a0003c0003t0001g0127a0003c0003t0002g0094a0003c0003t0002g0120others(10): Show | 13 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.541-7886dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27669833 | |||||
chr16:27670129
|
C | T | 5 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(2): Show | 5 | HG01109.hp2 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-7600C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27670129 | ||||||
chr16:27670345
|
A | G | 26 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(23): Show | 26 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.541-7384A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27670345 | ||||||
chr16:27670489
|
C | T | 1 | a0004c0034t0005g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.541-7240C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27670489 | ||||||
chr16:27670612
|
C | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.541-7117C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27670612 | ||||||
chr16:27670786
|
G | A | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.541-6943G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27670786 | ||||||
chr16:27670922
|
T | G | 1 | a0001c0026t0004g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.541-6807T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27670922 | ||||||
chr16:27671171
|
C | T | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.541-6558C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27671171 | ||||||
chr16:27671431
|
C | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-6298C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27671431 | ||||||
chr16:27671461
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.541-6268T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27671461 | ||||||
chr16:27671508
|
T | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0004g0005others(1): Show | 4 | HG02630.hp2 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-6221T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27671508 | ||||||
chr16:27671592
|
G | A | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.541-6137G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27671592 | ||||||
chr16:27671713
|
C | T | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.541-6016C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27671713 | ||||||
chr16:27671784
|
A | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-5945A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27671784 | ||||||
chr16:27671786
|
T | G | 1 | a0001c0001t0004g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.541-5943T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27671786 | ||||||
chr16:27671827
|
G | A | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.541-5902G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27671827 | ||||||
chr16:27671846
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.541-5883G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27671846 | ||||||
chr16:27671912
|
C | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-5817C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27671912 | ||||||
chr16:27671981
|
G | A | 1 | a0001c0004t0001g0116 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.541-5748G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27671981 | ||||||
chr16:27672263
|
G | C | 1 | a0001c0015t0001g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.541-5466G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27672263 | ||||||
chr16:27672833
|
AG | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | NA18747.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.541-4894delG | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr16 | 27672833 | |||||
chr16:27673079
|
T | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-4650T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27673079 | ||||||
chr16:27673289
|
G | A | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-4440G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27673289 | ||||||
chr16:27673507
|
A | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-4222A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27673507 | ||||||
chr16:27673518
|
G | A | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-4211G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27673518 | ||||||
chr16:27673599
|
A | T | 1 | a0003c0003t0002g0128 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.541-4130A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27673599 | ||||||
chr16:27673615
|
C | T | 1 | a0001c0001t0001g0010 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.541-4114C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27673615 | ||||||
chr16:27673785
|
C | T | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-3944C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27673785 | ||||||
chr16:27673906
|
C | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.541-3823C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27673906 | ||||||
chr16:27673950
|
C | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.541-3779C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27673950 | ||||||
chr16:27673998
|
C | CG | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-3731_541-3730i others(3): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27673998 | ||||||
chr16:27674000
|
G | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-3729G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27674000 | ||||||
chr16:27674010
|
G | A | 26 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(23): Show | 26 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.541-3719G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27674010 | ||||||
chr16:27674098
|
C | T | 1 | a0001c0001t0004g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.541-3631C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27674098 | ||||||
chr16:27674173
|
A | C | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.541-3556A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27674173 | ||||||
chr16:27674220
|
G | A | 3 | a0003c0003t0001g0127a0003c0003t0002g0126a0003c0003t0002g0129 | 3 | HG01261.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.541-3509G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27674220 | ||||||
chr16:27674319
|
T | A | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.541-3410T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27674319 | ||||||
chr16:27674900
|
G | A | 6 | a0001c0001t0004g0081a0001c0001t0006g0037a0001c0008t0004g0026others(3): Show | 6 | HG02109.hp1 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-2829G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27674900 | ||||||
chr16:27675184
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.541-2545A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27675184 | ||||||
chr16:27675221
|
C | T | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.541-2508C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27675221 | ||||||
chr16:27675693
|
G | A | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.541-2036G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27675693 | ||||||
chr16:27675697
|
T | C | 26 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(23): Show | 26 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.541-2032T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27675697 | ||||||
chr16:27676064
|
G | A | 41 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.541-1665G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27676064 | ||||||
chr16:27676109
|
A | G | 70 | a0001c0001t0002g0071a0001c0001t0004g0056a0001c0004t0001g0116others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.541-1620A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27676109 | ||||||
chr16:27676250
|
G | A | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-1479G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27676250 | ||||||
chr16:27676319
|
A | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-1410A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27676319 | ||||||
chr16:27676434
|
G | A | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.541-1295G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27676434 | ||||||
chr16:27676498
|
C | T | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-1231C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27676498 | ||||||
chr16:27676519
|
C | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-1210C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27676519 | ||||||
chr16:27676794
|
C | T | 2 | a0003c0003t0002g0094a0003c0003t0002g0121 | 2 | HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.541-935C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27676794 | ||||||
chr16:27676894
|
A | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.541-835A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27676894 | ||||||
chr16:27677424
|
A | G | 3 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0136 | 3 | HG02965.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.541-305A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 6/27 | chr16 | 27677424 | ||||||
chr16:27678638
|
T | C | 1 | a0001c0001t0001g0009 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.808+642T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27678638 | ||||||
chr16:27678661
|
A | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.808+665A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27678661 | ||||||
chr16:27678707
|
G | T | 2 | a0003c0003t0002g0123a0003c0003t0002g0139 | 2 | HG01358.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.808+711G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27678707 | ||||||
chr16:27678715
|
G | A | 2 | a0003c0003t0002g0094a0003c0003t0002g0121 | 2 | HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.808+719G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27678715 | ||||||
chr16:27678847
|
A | G | 41 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.808+851A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27678847 | ||||||
chr16:27678986
|
C | G | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.808+990C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27678986 | ||||||
chr16:27679283
|
C | T | 13 | a0003c0003t0001g0127a0003c0003t0002g0094a0003c0003t0002g0120others(10): Show | 13 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.808+1287C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27679283 | ||||||
chr16:27679309
|
C | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.808+1313C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27679309 | ||||||
chr16:27679344
|
G | A | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.808+1348G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27679344 | ||||||
chr16:27679749
|
CA | C | 9 | a0001c0001t0001g0038a0001c0005t0001g0144a0001c0005t0001g0145others(6): Show | 9 | HG02897.hp2 HG02970.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.809-1629delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr16 | 27679749 | |||||
chr16:27679749
|
CAAAA | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.809-1632_809-1629d others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr16 | 27679749 | |||||
chr16:27680082
|
G | C | 19 | a0001c0012t0002g0137a0001c0012t0002g0143a0001c0024t0001g0078others(16): Show | 19 | HG00408.hp1 HG02074.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.809-1317G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27680082 | ||||||
chr16:27680198
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.809-1201A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27680198 | ||||||
chr16:27680320
|
A | G | 41 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.809-1079A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27680320 | ||||||
chr16:27680340
|
G | A | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.809-1059G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27680340 | ||||||
chr16:27680483
|
A | G | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.809-916A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27680483 | ||||||
chr16:27680590
|
T | A | 1 | a0009c0014t0001g0043 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.809-809T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27680590 | ||||||
chr16:27680590
|
T | G | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.809-809T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27680590 | ||||||
chr16:27680670
|
G | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.809-729G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27680670 | ||||||
chr16:27680711
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.809-688C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27680711 | ||||||
chr16:27680803
|
T | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.809-596T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27680803 | ||||||
chr16:27680839
|
T | C | 73 | a0001c0001t0002g0071a0001c0004t0001g0116a0001c0004t0001g0117others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.809-560T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27680839 | ||||||
chr16:27680840
|
G | A | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.809-559G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27680840 | ||||||
chr16:27680879
|
A | G | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.809-520A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27680879 | ||||||
chr16:27681243
|
G | A | 3 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0136 | 3 | HG02965.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.809-156G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 7/27 | chr16 | 27681243 | ||||||
chr16:27681711
|
A | T | 1 | a0001c0001t0004g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.940+181A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27681711 | ||||||
chr16:27682024
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.940+494G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27682024 | ||||||
chr16:27682048
|
T | C | 41 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.940+518T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27682048 | ||||||
chr16:27682074
|
G | C | 2 | a0006c0009t0001g0035a0006c0009t0001g0036 | 2 | HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.940+544G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27682074 | ||||||
chr16:27682368
|
C | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.940+838C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27682368 | ||||||
chr16:27682556
|
G | C | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.940+1026G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27682556 | ||||||
chr16:27682683
|
G | A | 2 | a0003c0003t0002g0126a0003c0003t0002g0129 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.940+1153G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27682683 | ||||||
chr16:27682757
|
C | T | 1 | a0001c0026t0004g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.940+1227C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27682757 | ||||||
chr16:27682795
|
T | C | 42 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.940+1265T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27682795 | ||||||
chr16:27682846
|
A | C | 1 | a0001c0001t0008g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.940+1316A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27682846 | ||||||
chr16:27683219
|
T | G | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.940+1689T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27683219 | ||||||
chr16:27683234
|
C | T | 1 | a0006c0009t0001g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.940+1704C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27683234 | ||||||
chr16:27683491
|
G | A | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+1961G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27683491 | ||||||
chr16:27683529
|
A | G | 1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.940+1999A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27683529 | ||||||
chr16:27683544
|
A | G | 9 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(6): Show | 9 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.940+2014A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27683544 | ||||||
chr16:27683751
|
T | A | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.940+2221T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27683751 | ||||||
chr16:27683865
|
G | A | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+2335G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27683865 | ||||||
chr16:27683975
|
G | C | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.940+2445G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27683975 | ||||||
chr16:27683988
|
G | A | 14 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(11): Show | 14 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.940+2458G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27683988 | ||||||
chr16:27683989
|
G | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0004g0005others(1): Show | 4 | HG02630.hp2 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+2459G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27683989 | ||||||
chr16:27683998
|
G | A | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.940+2468G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27683998 | ||||||
chr16:27684313
|
A | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.940+2783A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27684313 | ||||||
chr16:27684579
|
A | G | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.940+3049A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27684579 | ||||||
chr16:27684857
|
A | G | 2 | a0003c0003t0002g0126a0003c0003t0002g0129 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.940+3327A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27684857 | ||||||
chr16:27684966
|
A | G | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+3436A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27684966 | ||||||
chr16:27685197
|
G | A | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.940+3667G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27685197 | ||||||
chr16:27685241
|
A | G | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.940+3711A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27685241 | ||||||
chr16:27685649
|
G | C | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.940+4119G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27685649 | ||||||
chr16:27685655
|
A | G | 4 | a0001c0004t0001g0132a0002c0002t0003g0134a0002c0002t0003g0135others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+4125A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27685655 | ||||||
chr16:27686451
|
T | G | 10 | a0001c0001t0001g0019a0001c0015t0001g0012a0001c0015t0001g0084others(7): Show | 10 | HG00741.hp2 HG01243.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.940+4921T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27686451 | ||||||
chr16:27686527
|
C | A | 1 | a0001c0001t0001g0009 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.940+4997C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27686527 | ||||||
chr16:27686543
|
C | T | 1 | a0001c0001t0004g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.940+5013C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27686543 | ||||||
chr16:27686916
|
T | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.940+5386T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27686916 | ||||||
chr16:27686981
|
G | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.940+5451G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27686981 | ||||||
chr16:27687298
|
CT | C | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.940+5778delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr16 | 27687298 | |||||
chr16:27687675
|
A | G | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.940+6145A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27687675 | ||||||
chr16:27688048
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.940+6518G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27688048 | ||||||
chr16:27688060
|
C | T | 1 | a0001c0001t0004g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.940+6530C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27688060 | ||||||
chr16:27688211
|
A | G | 42 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.940+6681A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27688211 | ||||||
chr16:27688242
|
C | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.940+6712C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27688242 | ||||||
chr16:27688585
|
C | T | 1 | a0001c0005t0002g0149 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.940+7055C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27688585 | ||||||
chr16:27688665
|
G | A | 23 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(20): Show | 23 | HG00408.hp1 HG01109.hp2 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.940+7135G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27688665 | ||||||
chr16:27689083
|
G | A | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.940+7553G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27689083 | ||||||
chr16:27689406
|
G | A | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.940+7876G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27689406 | ||||||
chr16:27689417
|
A | G | 2 | a0003c0003t0002g0123a0003c0003t0002g0139 | 2 | HG01358.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.940+7887A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27689417 | ||||||
chr16:27689425
|
T | A | 1 | a0001c0001t0001g0003 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.940+7895T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27689425 | ||||||
chr16:27689778
|
C | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.940+8248C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27689778 | ||||||
chr16:27689785
|
G | A | 1 | a0004c0007t0010g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.940+8255G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27689785 | ||||||
chr16:27689898
|
TTATTCTC | T | 3 | a0007c0010t0002g0112a0007c0010t0002g0113a0007c0010t0002g0114 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.940+8371_940+8377d others(9): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr16 | 27689898 | |||||
chr16:27690117
|
A | T | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.941-8211A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27690117 | ||||||
chr16:27690140
|
AAAT | A | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.941-8167_941-8165d others(5): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr16 | 27690140 | |||||
chr16:27690252
|
G | C | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.941-8076G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27690252 | ||||||
chr16:27690290
|
C | T | 2 | a0001c0028t0004g0109a0018c0025t0003g0111 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.941-8038C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27690290 | ||||||
chr16:27690315
|
C | CAGAT | 44 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0020others(41): Show | 44 | HG00408.hp2 HG00741.hp1 HG01361.hp2 others(41): Show |
intron_variant | MODIFIER | c.941-7968_941-7965d others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr16 | 27690315 | |||||
chr16:27690315
|
C | CAGATAGA others(1): Show |
16 | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0044others(13): Show | 16 | HG00408.hp1 HG01517.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.941-7972_941-7965d others(10): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr16 | 27690315 | |||||
chr16:27690315
|
C | CAGATAGA others(5): Show |
7 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0057others(4): Show | 7 | HG00140.hp2 HG01106.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.941-7976_941-7965d others(14): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr16 | 27690315 | |||||
chr16:27690315
|
CAGAT | C | 16 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0004g0081others(13): Show | 16 | HG01243.hp1 HG01258.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.941-7968_941-7965d others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr16 | 27690315 | |||||
chr16:27690340
|
AGATAGAT others(16): Show |
A | 2 | a0001c0005t0002g0147a0003c0003t0002g0120 | 2 | HG00140.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.941-7964_941-7942d others(25): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr16 | 27690340 | |||||
chr16:27690344
|
AGATAGAT others(12): Show |
A | 5 | a0001c0005t0002g0148a0001c0011t0002g0141a0001c0011t0002g0152others(2): Show | 5 | HG01243.hp2 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.941-7964_941-7946d others(21): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr16 | 27690344 | |||||
chr16:27690348
|
AGATAGAT others(8): Show |
A | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(2): Show | 5 | HG02280.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.941-7964_941-7950d others(17): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr16 | 27690348 | |||||
chr16:27690352
|
AGATAGAT others(4): Show |
A | 10 | a0001c0018t0011g0122a0003c0003t0001g0127a0003c0003t0002g0125others(7): Show | 10 | HG00099.hp1 HG01106.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.941-7964_941-7954d others(13): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr16 | 27690352 | |||||
chr16:27690356
|
AGATAGAT | A | 6 | a0003c0003t0002g0094a0003c0003t0002g0121a0003c0003t0002g0123others(3): Show | 6 | HG01258.hp2 HG01358.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.941-7964_941-7958d others(9): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr16 | 27690356 | |||||
chr16:27690359
|
TA | T | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-7968delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27690359 | ||||||
chr16:27690363
|
T | TA | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-7965_941-7964i others(3): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27690363 | ||||||
chr16:27690363
|
T | TAGATAGA others(21): Show |
2 | a0001c0001t0001g0010a0004c0030t0005g0115 | 2 | HG03041.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.941-7965_941-7964i others(30): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27690363 | ||||||
chr16:27690363
|
T | TAGATAGA others(17): Show |
1 | a0001c0001t0001g0002 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.941-7965_941-7964i others(26): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27690363 | ||||||
chr16:27690363
|
T | TAGATAGA others(9): Show |
4 | a0001c0001t0001g0015a0001c0001t0001g0089a0001c0001t0009g0055others(1): Show | 4 | HG02155.hp2 HG02165.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.941-7965_941-7964i others(18): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27690363 | ||||||
chr16:27690363
|
T | TAGATAGA others(13): Show |
2 | a0001c0001t0001g0009a0001c0001t0001g0095 | 2 | NA19002.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.941-7965_941-7964i others(22): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27690363 | ||||||
chr16:27690363
|
T | TAGATAGA others(5): Show |
4 | a0001c0001t0001g0003a0001c0001t0004g0024a0011c0017t0005g0151others(1): Show | 4 | HG01358.hp1 HG02109.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-7965_941-7964i others(14): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27690363 | ||||||
chr16:27690363
|
T | TAGATGAT others(1): Show |
2 | a0001c0004t0001g0042a0004c0034t0005g0119 | 2 | HG00099.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.941-7965_941-7964i others(10): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27690363 | ||||||
chr16:27690386
|
T | A | 4 | a0003c0003t0002g0125a0003c0003t0002g0130a0003c0003t0002g0131others(1): Show | 4 | HG01258.hp2 HG01361.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-7942T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27690386 | ||||||
chr16:27690624
|
C | T | 13 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.941-7704C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27690624 | ||||||
chr16:27690780
|
G | A | 2 | a0010c0013t0003g0061a0010c0013t0003g0103 | 2 | NA19000.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.941-7548G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27690780 | ||||||
chr16:27690810
|
T | C | 60 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.941-7518T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27690810 | ||||||
chr16:27690956
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | NA18747.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.941-7372G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27690956 | ||||||
chr16:27691002
|
A | C | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.941-7326A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27691002 | ||||||
chr16:27691275
|
C | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.941-7053C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27691275 | ||||||
chr16:27691416
|
G | A | 19 | a0001c0012t0002g0137a0001c0012t0002g0143a0001c0024t0001g0078others(16): Show | 19 | HG00408.hp1 HG02074.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.941-6912G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27691416 | ||||||
chr16:27691449
|
A | G | 73 | a0001c0001t0002g0071a0001c0004t0001g0116a0001c0004t0001g0117others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.941-6879A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27691449 | ||||||
chr16:27691574
|
G | A | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.941-6754G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27691574 | ||||||
chr16:27691623
|
C | T | 1 | a0001c0024t0001g0078 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.941-6705C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27691623 | ||||||
chr16:27691700
|
A | G | 3 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0136 | 3 | HG02965.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.941-6628A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27691700 | ||||||
chr16:27691788
|
G | A | 16 | a0001c0024t0001g0078a0002c0002t0003g0062a0002c0002t0003g0063others(13): Show | 16 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.941-6540G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27691788 | ||||||
chr16:27691918
|
A | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.941-6410A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27691918 | ||||||
chr16:27691929
|
A | G | 60 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.941-6399A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27691929 | ||||||
chr16:27691932
|
C | T | 19 | a0001c0012t0002g0137a0001c0012t0002g0143a0001c0024t0001g0078others(16): Show | 19 | HG00408.hp1 HG02074.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.941-6396C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27691932 | ||||||
chr16:27692108
|
G | A | 1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.941-6220G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27692108 | ||||||
chr16:27692416
|
C | G | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.941-5912C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27692416 | ||||||
chr16:27692650
|
C | T | 19 | a0001c0012t0002g0137a0001c0012t0002g0143a0001c0024t0001g0078others(16): Show | 19 | HG00408.hp1 HG02074.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.941-5678C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27692650 | ||||||
chr16:27692651
|
G | A | 11 | a0001c0001t0001g0053a0001c0001t0002g0011a0001c0001t0002g0014others(8): Show | 11 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.941-5677G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27692651 | ||||||
chr16:27692667
|
A | G | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-5661A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27692667 | ||||||
chr16:27692714
|
A | G | 58 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.941-5614A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27692714 | ||||||
chr16:27692750
|
C | G | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.941-5578C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27692750 | ||||||
chr16:27692798
|
G | C | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.941-5530G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27692798 | ||||||
chr16:27693047
|
A | AG | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.941-5279dupG | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr16 | 27693047 | |||||
chr16:27693450
|
A | G | 112 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0029others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.941-4878A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27693450 | ||||||
chr16:27693580
|
G | A | 1 | a0001c0001t0004g0056 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.941-4748G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27693580 | ||||||
chr16:27693680
|
C | T | 6 | a0005c0006t0001g0013a0005c0006t0001g0058a0005c0006t0001g0059others(3): Show | 6 | HG00741.hp2 HG01243.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.941-4648C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27693680 | ||||||
chr16:27693681
|
G | A | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.941-4647G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27693681 | ||||||
chr16:27693761
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.941-4567C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27693761 | ||||||
chr16:27693816
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.941-4512G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27693816 | ||||||
chr16:27693825
|
T | C | 41 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.941-4503T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27693825 | ||||||
chr16:27694220
|
A | G | 39 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.941-4108A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27694220 | ||||||
chr16:27694610
|
A | T | 2 | a0007c0010t0002g0112a0007c0010t0002g0113 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.941-3718A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27694610 | ||||||
chr16:27694667
|
A | G | 59 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.941-3661A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27694667 | ||||||
chr16:27694791
|
C | CAATA | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(25): Show | 28 | HG00099.hp2 HG00408.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.941-3509_941-3506d others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr16 | 27694791 | |||||
chr16:27694791
|
C | CAATAAAT others(1): Show |
5 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0001g0090others(2): Show | 5 | HG01106.hp2 HG02155.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.941-3513_941-3506d others(10): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr16 | 27694791 | |||||
chr16:27694807
|
A | T | 25 | a0003c0003t0001g0127a0003c0003t0002g0094a0003c0003t0002g0120others(22): Show | 25 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.941-3521A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27694807 | ||||||
chr16:27694811
|
A | T | 39 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.941-3517A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27694811 | ||||||
chr16:27694815
|
A | T | 40 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.941-3513A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27694815 | ||||||
chr16:27694819
|
A | T | 40 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.941-3509A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27694819 | ||||||
chr16:27695000
|
C | T | 40 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.941-3328C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27695000 | ||||||
chr16:27695001
|
G | A | 1 | a0001c0001t0009g0055 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.941-3327G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27695001 | ||||||
chr16:27695204
|
A | T | 1 | a0001c0001t0002g0027 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.941-3124A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27695204 | ||||||
chr16:27695320
|
C | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.941-3008C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27695320 | ||||||
chr16:27695510
|
C | A | 3 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0136 | 3 | HG02965.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.941-2818C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27695510 | ||||||
chr16:27695573
|
T | A | 41 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.941-2755T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27695573 | ||||||
chr16:27696008
|
G | A | 19 | a0001c0012t0002g0137a0001c0012t0002g0143a0001c0024t0001g0078others(16): Show | 19 | HG00408.hp1 HG02074.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.941-2320G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27696008 | ||||||
chr16:27696373
|
A | G | 61 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.941-1955A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27696373 | ||||||
chr16:27696453
|
A | G | 4 | a0001c0004t0001g0132a0002c0002t0003g0134a0002c0002t0003g0135others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-1875A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27696453 | ||||||
chr16:27696579
|
G | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.941-1749G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27696579 | ||||||
chr16:27696832
|
G | A | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.941-1496G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27696832 | ||||||
chr16:27696881
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.941-1447A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27696881 | ||||||
chr16:27696895
|
A | T | 1 | a0001c0001t0001g0039 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.941-1433A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27696895 | ||||||
chr16:27697025
|
G | A | 12 | a0001c0001t0001g0019a0001c0001t0008g0050a0001c0015t0001g0012others(9): Show | 12 | HG00741.hp2 HG01243.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.941-1303G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27697025 | ||||||
chr16:27697079
|
C | A | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.941-1249C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27697079 | ||||||
chr16:27697152
|
T | A | 2 | a0001c0011t0002g0141a0001c0011t0002g0152 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.941-1176T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27697152 | ||||||
chr16:27697445
|
T | C | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.941-883T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27697445 | ||||||
chr16:27697487
|
A | G | 1 | a0001c0001t0007g0091 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.941-841A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27697487 | ||||||
chr16:27697608
|
A | T | 6 | a0001c0001t0004g0081a0001c0001t0006g0037a0001c0008t0004g0026others(3): Show | 6 | HG02109.hp1 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.941-720A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27697608 | ||||||
chr16:27697621
|
A | T | 1 | a0001c0001t0001g0007 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.941-707A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27697621 | ||||||
chr16:27697631
|
ATAT | A | 9 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(6): Show | 9 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.941-693_941-691del others(3): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr16 | 27697631 | |||||
chr16:27698127
|
C | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.941-201C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 8/27 | chr16 | 27698127 | ||||||
chr16:27698504
|
C | G | 1 | a0001c0001t0001g0022 | 1 | HG01978.hp1 | splice_region_variant&intron_variant | LOW | c.1113+4C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 9/27 | chr16 | 27698504 | ||||||
chr16:27698504
|
C | T | 40 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(37): Show |
splice_region_variant&intron_variant | LOW | c.1113+4C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 9/27 | chr16 | 27698504 | ||||||
chr16:27698505
|
G | A | 1 | a0001c0001t0008g0050 | 1 | HG02970.hp2 | splice_region_variant&intron_variant | LOW | c.1113+5G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 9/27 | chr16 | 27698505 | ||||||
chr16:27698510
|
G | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1113+10G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 9/27 | chr16 | 27698510 | ||||||
chr16:27698688
|
T | G | 1 | a0001c0012t0002g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1113+188T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 9/27 | chr16 | 27698688 | ||||||
chr16:27698689
|
T | C | 1 | a0001c0012t0002g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1113+189T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 9/27 | chr16 | 27698689 | ||||||
chr16:27698713
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1113+213G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 9/27 | chr16 | 27698713 | ||||||
chr16:27698803
|
T | C | 40 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.1113+303T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 9/27 | chr16 | 27698803 | ||||||
chr16:27699005
|
AGGAGGAT others(4): Show |
A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1113+508_1114-516d others(13): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr16 | 27699005 | |||||
chr16:27699025
|
G | C | 1 | a0003c0003t0002g0125 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1114-509G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 9/27 | chr16 | 27699025 | ||||||
chr16:27699075
|
G | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1114-459G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 9/27 | chr16 | 27699075 | ||||||
chr16:27699109
|
G | T | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1114-425G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 9/27 | chr16 | 27699109 | ||||||
chr16:27699918
|
T | TA | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1179+319_1179+320i others(3): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 10/27 | chr16 | 27699918 | ||||||
chr16:27699919
|
T | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.1179+320T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 10/27 | chr16 | 27699919 | ||||||
chr16:27699973
|
C | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1179+374C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 10/27 | chr16 | 27699973 | ||||||
chr16:27700055
|
C | T | 19 | a0001c0012t0002g0137a0001c0012t0002g0143a0001c0024t0001g0078others(16): Show | 19 | HG00408.hp1 HG02074.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1179+456C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 10/27 | chr16 | 27700055 | ||||||
chr16:27700158
|
C | T | 1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1179+559C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 10/27 | chr16 | 27700158 | ||||||
chr16:27700217
|
T | G | 1 | a0001c0001t0001g0086 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1179+618T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 10/27 | chr16 | 27700217 | ||||||
chr16:27700361
|
A | T | 1 | a0003c0003t0002g0121 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1179+762A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 10/27 | chr16 | 27700361 | ||||||
chr16:27700405
|
C | T | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1179+806C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 10/27 | chr16 | 27700405 | ||||||
chr16:27700432
|
G | A | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1179+833G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 10/27 | chr16 | 27700432 | ||||||
chr16:27700755
|
G | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1180-834G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 10/27 | chr16 | 27700755 | ||||||
chr16:27700967
|
A | G | 98 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0002g0071others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1180-622A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 10/27 | chr16 | 27700967 | ||||||
chr16:27701021
|
C | T | 61 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1180-568C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 10/27 | chr16 | 27701021 | ||||||
chr16:27701088
|
T | C | 40 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.1180-501T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 10/27 | chr16 | 27701088 | ||||||
chr16:27701161
|
T | A | 1 | a0001c0001t0004g0056 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1180-428T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 10/27 | chr16 | 27701161 | ||||||
chr16:27701206
|
G | A | 1 | a0001c0023t0001g0060 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1180-383G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 10/27 | chr16 | 27701206 | ||||||
chr16:27701232
|
A | C | 13 | a0003c0003t0001g0127a0003c0003t0002g0094a0003c0003t0002g0120others(10): Show | 13 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1180-357A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 10/27 | chr16 | 27701232 | ||||||
chr16:27701315
|
G | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1180-274G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 10/27 | chr16 | 27701315 | ||||||
chr16:27701721
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1286+26C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27701721 | ||||||
chr16:27701781
|
A | G | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1286+86A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27701781 | ||||||
chr16:27701782
|
C | T | 27 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(24): Show | 27 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1286+87C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27701782 | ||||||
chr16:27701911
|
G | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1286+216G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27701911 | ||||||
chr16:27701977
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1286+282A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27701977 | ||||||
chr16:27702125
|
C | G | 1 | a0001c0026t0004g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1286+430C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27702125 | ||||||
chr16:27702374
|
C | T | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1286+679C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27702374 | ||||||
chr16:27702448
|
T | C | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1286+753T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27702448 | ||||||
chr16:27702542
|
A | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1286+847A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27702542 | ||||||
chr16:27702559
|
A | G | 1 | a0001c0001t0001g0038 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1286+864A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27702559 | ||||||
chr16:27702769
|
G | A | 1 | a0017c0021t0001g0016 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1286+1074G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27702769 | ||||||
chr16:27702842
|
G | C | 1 | a0001c0001t0004g0025 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1287-1054G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27702842 | ||||||
chr16:27702895
|
A | G | 61 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1287-1001A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27702895 | ||||||
chr16:27702900
|
C | T | 1 | a0017c0021t0001g0016 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1287-996C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27702900 | ||||||
chr16:27702964
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1287-932C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27702964 | ||||||
chr16:27703134
|
T | G | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1287-762T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27703134 | ||||||
chr16:27703263
|
T | C | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1287-633T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27703263 | ||||||
chr16:27703265
|
G | C | 40 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.1287-631G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27703265 | ||||||
chr16:27703575
|
G | A | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1287-321G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27703575 | ||||||
chr16:27703854
|
C | T | 19 | a0001c0012t0002g0137a0001c0012t0002g0143a0001c0024t0001g0078others(16): Show | 19 | HG00408.hp1 HG02074.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1287-42C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 11/27 | chr16 | 27703854 | ||||||
chr16:27704056
|
AT | A | 40 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.1389+61delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr16 | 27704056 | |||||
chr16:27704074
|
T | C | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1389+76T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27704074 | ||||||
chr16:27704098
|
C | T | 1 | a0001c0001t0001g0010 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1389+100C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27704098 | ||||||
chr16:27704122
|
G | GC | 19 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0053others(16): Show | 19 | HG00408.hp2 HG00741.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.1389+133dupC | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr16 | 27704122 | |||||
chr16:27704123
|
C | T | 19 | a0001c0012t0002g0137a0001c0012t0002g0143a0001c0024t0001g0078others(16): Show | 19 | HG00408.hp1 HG02074.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1389+125C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27704123 | ||||||
chr16:27704125
|
C | A | 4 | a0001c0001t0002g0014a0001c0001t0002g0033a0001c0001t0002g0046others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389+127C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27704125 | ||||||
chr16:27704131
|
C | T | 1 | a0002c0002t0003g0097 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1389+133C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27704131 | ||||||
chr16:27704205
|
A | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1389+207A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27704205 | ||||||
chr16:27704649
|
A | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1389+651A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27704649 | ||||||
chr16:27704906
|
C | CT | 5 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0082others(2): Show | 5 | HG01978.hp1 HG02273.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1389+928dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr16 | 27704906 | |||||
chr16:27704906
|
CTTTTTTT | C | 11 | a0001c0001t0004g0005a0001c0005t0001g0144a0001c0005t0001g0145others(8): Show | 11 | HG02886.hp1 HG02896.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.1389+922_1389+928d others(9): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr16 | 27704906 | |||||
chr16:27705060
|
A | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1389+1062A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27705060 | ||||||
chr16:27705248
|
A | G | 9 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(6): Show | 9 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1389+1250A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27705248 | ||||||
chr16:27705325
|
C | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1389+1327C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27705325 | ||||||
chr16:27705326
|
G | A | 2 | a0001c0001t0004g0017a0009c0014t0001g0043 | 2 | HG01258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1389+1328G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27705326 | ||||||
chr16:27705526
|
G | A | 1 | a0001c0001t0001g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1389+1528G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27705526 | ||||||
chr16:27705561
|
A | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1389+1563A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27705561 | ||||||
chr16:27705614
|
C | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1389+1616C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27705614 | ||||||
chr16:27705797
|
T | C | 1 | a0002c0002t0003g0110 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1389+1799T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27705797 | ||||||
chr16:27706033
|
A | C | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1389+2035A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27706033 | ||||||
chr16:27706144
|
A | AAGCTCAG others(13): Show |
8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1389+2159_1389+217 others(24): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr16 | 27706144 | |||||
chr16:27706144
|
A | AAGCTCAG others(13): Show |
1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1389+2161_1389+216 others(24): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr16 | 27706144 | |||||
chr16:27706294
|
G | A | 3 | a0001c0012t0002g0137a0001c0012t0002g0143a0014c0019t0003g0100 | 3 | HG02109.hp2 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1389+2296G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27706294 | ||||||
chr16:27706455
|
C | A | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1390-2250C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27706455 | ||||||
chr16:27706618
|
G | A | 45 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.1390-2087G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27706618 | ||||||
chr16:27706736
|
C | T | 3 | a0001c0012t0002g0137a0001c0012t0002g0143a0014c0019t0003g0100 | 3 | HG02109.hp2 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1390-1969C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27706736 | ||||||
chr16:27706938
|
G | C | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1390-1767G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27706938 | ||||||
chr16:27706976
|
G | C | 2 | a0001c0012t0002g0137a0001c0012t0002g0143 | 2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1390-1729G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27706976 | ||||||
chr16:27707085
|
A | T | 3 | a0007c0010t0002g0112a0007c0010t0002g0113a0007c0010t0002g0114 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1390-1620A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27707085 | ||||||
chr16:27707140
|
G | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1390-1565G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27707140 | ||||||
chr16:27707212
|
A | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1390-1493A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27707212 | ||||||
chr16:27707417
|
C | T | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1390-1288C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27707417 | ||||||
chr16:27707784
|
C | A | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1390-921C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27707784 | ||||||
chr16:27707841
|
T | G | 1 | a0012c0033t0002g0142 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1390-864T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27707841 | ||||||
chr16:27707901
|
A | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1390-804A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27707901 | ||||||
chr16:27708024
|
C | CT | 48 | a0001c0001t0001g0028a0001c0004t0001g0116a0001c0004t0001g0117others(45): Show | 48 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.1390-665dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr16 | 27708024 | |||||
chr16:27708168
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0095 | 2 | NA19002.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1390-537C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27708168 | ||||||
chr16:27708336
|
C | T | 3 | a0001c0012t0002g0137a0001c0012t0002g0143a0014c0019t0003g0100 | 3 | HG02109.hp2 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1390-369C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 12/27 | chr16 | 27708336 | ||||||
chr16:27708985
|
G | A | 45 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.1605+65G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27708985 | ||||||
chr16:27709002
|
G | A | 4 | a0002c0002t0003g0063a0002c0002t0003g0067a0010c0013t0003g0061others(1): Show | 4 | NA18950.hp1 NA18954.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1605+82G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27709002 | ||||||
chr16:27709104
|
A | G | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1605+184A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27709104 | ||||||
chr16:27709143
|
A | T | 1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1605+223A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27709143 | ||||||
chr16:27709321
|
T | TAA | 8 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(5): Show | 8 | HG02897.hp2 HG02970.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1605+416_1605+417d others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27709321 | |||||
chr16:27709343
|
C | T | 1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1605+423C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27709343 | ||||||
chr16:27709390
|
G | T | 1 | a0001c0001t0004g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1605+470G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27709390 | ||||||
chr16:27709435
|
A | G | 1 | a0001c0012t0002g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1605+515A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27709435 | ||||||
chr16:27709643
|
AAAAT | A | 4 | a0001c0001t0002g0011a0001c0001t0002g0034a0001c0001t0002g0040others(1): Show | 4 | HG02258.hp2 HG02280.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1605+730_1605+733d others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27709643 | |||||
chr16:27709742
|
C | T | 1 | a0004c0030t0005g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1605+822C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27709742 | ||||||
chr16:27710400
|
G | T | 1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1605+1480G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27710400 | ||||||
chr16:27710520
|
T | C | 27 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(24): Show | 27 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1605+1600T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27710520 | ||||||
chr16:27711131
|
C | T | 1 | a0001c0004t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1605+2211C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27711131 | ||||||
chr16:27711204
|
G | A | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1605+2284G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27711204 | ||||||
chr16:27711219
|
G | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1605+2299G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27711219 | ||||||
chr16:27711455
|
A | C | 2 | a0001c0012t0002g0137a0001c0012t0002g0143 | 2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1605+2535A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27711455 | ||||||
chr16:27711784
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1605+2864T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27711784 | ||||||
chr16:27712650
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1605+3730C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27712650 | ||||||
chr16:27712671
|
C | T | 1 | a0005c0006t0001g0059 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1605+3751C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27712671 | ||||||
chr16:27712904
|
C | G | 3 | a0001c0012t0002g0137a0001c0012t0002g0143a0014c0019t0003g0100 | 3 | HG02109.hp2 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1605+3984C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27712904 | ||||||
chr16:27712915
|
C | A | 10 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(7): Show | 10 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1605+3995C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27712915 | ||||||
chr16:27713552
|
G | A | 1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1605+4632G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713552 | ||||||
chr16:27713641
|
T | TTATGTGT others(218): Show |
1 | a0001c0001t0001g0015 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1605+4745_1605+474 others(229): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(216): Show |
1 | a0001c0001t0001g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1605+4745_1605+474 others(227): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(218): Show |
1 | a0001c0001t0001g0047 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1605+4745_1605+474 others(229): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(216): Show |
2 | a0001c0001t0001g0039a0001c0001t0001g0057 | 2 | HG00140.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1605+4745_1605+474 others(227): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(217): Show |
1 | a0001c0004t0001g0042 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1605+4745_1605+474 others(228): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(144): Show |
1 | a0001c0001t0004g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1605+4745_1605+474 others(155): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(218): Show |
1 | a0013c0027t0001g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1605+4745_1605+474 others(229): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(218): Show |
5 | a0001c0001t0001g0007a0001c0008t0004g0041a0001c0015t0001g0012others(2): Show | 5 | HG02155.hp1 HG02738.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1605+4745_1605+474 others(229): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(219): Show |
7 | a0005c0006t0001g0013a0005c0006t0001g0058a0005c0006t0001g0059others(4): Show | 7 | HG00741.hp2 HG01243.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1605+4745_1605+474 others(230): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(181): Show |
2 | a0001c0001t0001g0022a0001c0001t0001g0083 | 2 | HG01978.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1605+4745_1605+474 others(192): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(218): Show |
32 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(29): Show | 32 | HG00408.hp2 HG01106.hp2 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1605+4745_1605+474 others(229): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(255): Show |
1 | a0001c0001t0008g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1605+4745_1605+474 others(266): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(218): Show |
2 | a0001c0001t0001g0009a0001c0001t0001g0095 | 2 | NA19002.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1605+4745_1605+474 others(229): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(216): Show |
1 | a0001c0001t0004g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1605+4745_1605+474 others(227): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(216): Show |
1 | a0001c0001t0001g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1605+4745_1605+474 others(227): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(216): Show |
7 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0001g0093others(4): Show | 7 | HG00741.hp1 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1605+4745_1605+474 others(227): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(253): Show |
2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1605+4745_1605+474 others(264): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(252): Show |
1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1605+4808_1605+480 others(263): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(134): Show |
3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1605+4796_1605+479 others(145): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713641
|
T | TTATGTGT others(137): Show |
20 | a0001c0018t0011g0122a0001c0028t0004g0109a0003c0003t0002g0094others(17): Show | 20 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.1605+4796_1605+479 others(148): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713641 | |||||
chr16:27713647
|
G | GTGTGTAT others(107): Show |
1 | a0001c0001t0002g0014 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1605+4745_1605+474 others(118): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713647 | |||||
chr16:27713647
|
G | GTGTGTAT others(107): Show |
6 | a0001c0001t0002g0011a0001c0001t0002g0027a0001c0001t0002g0034others(3): Show | 6 | HG02145.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1605+4745_1605+474 others(118): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713647 | |||||
chr16:27713647
|
G | GTGTGTAT others(105): Show |
2 | a0001c0001t0002g0048a0001c0001t0002g0088 | 2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1605+4745_1605+474 others(116): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713647 | |||||
chr16:27713666
|
T | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0002g0033 | 3 | HG02922.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1605+4746T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713666 | ||||||
chr16:27713703
|
T | C | 3 | a0001c0001t0002g0014a0001c0001t0002g0046a0001c0001t0002g0048 | 3 | HG02451.hp2 HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1605+4783T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713703 | ||||||
chr16:27713703
|
T | TACATATT others(173): Show |
3 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0136 | 3 | HG02965.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1605+4808_1605+480 others(184): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713703 | |||||
chr16:27713703
|
T | TACATATT others(171): Show |
1 | a0001c0004t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1605+4808_1605+480 others(182): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713703 | |||||
chr16:27713705
|
C | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1605+4785C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713705 | ||||||
chr16:27713712
|
T | A | 5 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1605+4792T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713712 | ||||||
chr16:27713717
|
A | G | 12 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(9): Show | 12 | HG01261.hp2 HG01358.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.1605+4797A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713717 | ||||||
chr16:27713721
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1605+4801G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713721 | ||||||
chr16:27713725
|
G | A | 12 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(9): Show | 12 | HG01261.hp2 HG01358.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.1605+4805G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713725 | ||||||
chr16:27713727
|
AT | A | 12 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(9): Show | 12 | HG01261.hp2 HG01358.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.1605+4809delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713727 | |||||
chr16:27713728
|
T | TA | 48 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(45): Show | 48 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.1605+4808_1605+480 others(5): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713728 | ||||||
chr16:27713728
|
T | TATATATA others(71): Show |
1 | a0001c0001t0002g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1605+4808_1605+480 others(82): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713728 | ||||||
chr16:27713728
|
T | TATATATA others(212): Show |
10 | a0001c0024t0001g0078a0002c0002t0003g0062a0002c0002t0003g0063others(7): Show | 10 | HG00408.hp1 HG02132.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.1605+4808_1605+480 others(223): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713728 | ||||||
chr16:27713728
|
T | TATATATA others(179): Show |
1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1605+4808_1605+480 others(190): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713728 | ||||||
chr16:27713728
|
T | TATATATA others(253): Show |
1 | a0001c0012t0002g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1605+4808_1605+480 others(264): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713728 | ||||||
chr16:27713728
|
T | TATATATA others(140): Show |
1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1605+4808_1605+480 others(151): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713728 | ||||||
chr16:27713728
|
T | TATATATA others(175): Show |
2 | a0004c0030t0005g0115a0011c0017t0005g0150 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1605+4808_1605+480 others(186): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713728 | ||||||
chr16:27713728
|
T | TATATATA others(252): Show |
1 | a0001c0004t0001g0138 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1605+4808_1605+480 others(263): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713728 | ||||||
chr16:27713728
|
T | TATATATA others(27): Show |
1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1605+4808_1605+480 others(38): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713728 | ||||||
chr16:27713739
|
T | C | 1 | a0001c0001t0002g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1605+4819T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713739 | ||||||
chr16:27713739
|
T | TACATATT others(215): Show |
1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1605+4846_1605+484 others(226): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713739 | |||||
chr16:27713757
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1605+4837G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713757 | ||||||
chr16:27713767
|
G | A | 38 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(35): Show | 38 | HG01261.hp2 HG01358.hp2 HG02074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1605+4847G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713767 | ||||||
chr16:27713772
|
T | C | 38 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(35): Show | 38 | HG01261.hp2 HG01358.hp2 HG02074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1605+4852T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713772 | ||||||
chr16:27713774
|
T | C | 38 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(35): Show | 38 | HG01261.hp2 HG01358.hp2 HG02074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1605+4854T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713774 | ||||||
chr16:27713776
|
C | T | 38 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(35): Show | 38 | HG01261.hp2 HG01358.hp2 HG02074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1605+4856C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713776 | ||||||
chr16:27713780
|
TA | T | 3 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118 | 3 | HG02922.hp2 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1605+4861delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713780 | ||||||
chr16:27713781
|
AT | A | 2 | a0001c0011t0002g0141a0001c0011t0002g0152 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1605+4863delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713781 | |||||
chr16:27713784
|
A | G | 1 | a0012c0033t0002g0142 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1605+4864A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713784 | ||||||
chr16:27713786
|
A | G | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1605+4866A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713786 | ||||||
chr16:27713788
|
A | ATG | 2 | a0001c0001t0002g0071a0014c0019t0003g0100 | 2 | HG02109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1605+4882_1605+488 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713788 | |||||
chr16:27713788
|
A | G | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1605+4868A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713788 | ||||||
chr16:27713790
|
G | A | 33 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(30): Show | 33 | HG02074.hp1 HG02145.hp1 HG02258.hp2 others(30): Show |
intron_variant | MODIFIER | c.1605+4870G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713790 | ||||||
chr16:27713798
|
G | A | 5 | a0003c0003t0001g0127a0003c0003t0002g0123a0003c0003t0002g0139others(2): Show | 5 | HG01261.hp2 HG01358.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1605+4878G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713798 | ||||||
chr16:27713800
|
G | A | 37 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(34): Show | 37 | HG01261.hp2 HG01358.hp2 HG02074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1605+4880G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713800 | ||||||
chr16:27713800
|
GTGTATAT others(3): Show |
G | 1 | a0001c0001t0008g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1605+4882_1605+489 others(14): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713800 | |||||
chr16:27713802
|
G | A | 38 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(35): Show | 38 | HG01261.hp2 HG01358.hp2 HG02074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1605+4882G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713802 | ||||||
chr16:27713802
|
GTATATAC others(1): Show |
G | 2 | a0001c0018t0011g0122a0011c0017t0005g0150 | 2 | HG01106.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1605+4889_1605+489 others(12): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713802 | |||||
chr16:27713802
|
GTATATAC others(3): Show |
G | 2 | a0001c0004t0001g0138a0003c0003t0002g0120 | 2 | HG00140.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.1605+4889_1605+489 others(14): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713802 | |||||
chr16:27713802
|
GTATATAC others(5): Show |
G | 2 | a0002c0002t0003g0099a0002c0002t0003g0102 | 2 | NA18971.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1605+4889_1605+490 others(16): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713802 | |||||
chr16:27713802
|
GTATATAC others(7): Show |
G | 3 | a0002c0002t0003g0062a0008c0016t0001g0077a0010c0013t0003g0061 | 3 | HG02132.hp2 HG03516.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1605+4889_1605+490 others(18): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713802 | |||||
chr16:27713802
|
GTATATAC others(9): Show |
G | 11 | a0001c0024t0001g0078a0002c0002t0003g0063a0002c0002t0003g0065others(8): Show | 11 | HG00408.hp1 HG02135.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.1605+4889_1605+490 others(20): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713802 | |||||
chr16:27713802
|
GTATATAC others(11): Show |
G | 2 | a0004c0007t0001g0105a0008c0031t0001g0107 | 2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1605+4889_1605+490 others(22): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713802 | |||||
chr16:27713802
|
GTATATAC others(13): Show |
G | 8 | a0003c0003t0002g0094a0003c0003t0002g0121a0003c0003t0002g0125others(5): Show | 8 | HG01258.hp2 HG01361.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.1605+4889_1605+490 others(24): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713802 | |||||
chr16:27713803
|
TATATAC | T | 2 | a0001c0012t0002g0137a0001c0028t0004g0109 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1605+4889_1605+489 others(10): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713803 | |||||
chr16:27713804
|
A | G | 7 | a0001c0011t0002g0141a0001c0011t0002g0152a0001c0012t0002g0143others(4): Show | 7 | HG00099.hp1 HG01243.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1605+4884A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713804 | ||||||
chr16:27713805
|
TATAC | T | 2 | a0003c0003t0002g0128a0004c0030t0005g0115 | 2 | HG00099.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1605+4889_1605+489 others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713805 | |||||
chr16:27713806
|
A | G | 4 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142others(1): Show | 4 | HG01243.hp2 HG02486.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1605+4886A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713806 | ||||||
chr16:27713807
|
T | C | 5 | a0003c0003t0001g0127a0003c0003t0002g0123a0003c0003t0002g0139others(2): Show | 5 | HG01261.hp2 HG01358.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1605+4887T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713807 | ||||||
chr16:27713808
|
A | G | 2 | a0001c0011t0002g0141a0012c0033t0002g0142 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1605+4888A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713808 | ||||||
chr16:27713809
|
C | CAT | 11 | a0001c0001t0001g0039a0001c0001t0004g0017a0001c0001t0004g0049others(8): Show | 11 | HG01243.hp1 HG01261.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1605+4936_1605+493 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713809 | |||||
chr16:27713809
|
C | T | 4 | a0001c0011t0002g0141a0001c0011t0002g0152a0001c0012t0002g0143others(1): Show | 4 | HG01243.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1605+4889C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713809 | ||||||
chr16:27713809
|
CAT | C | 8 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0028others(5): Show | 8 | HG02155.hp2 HG02683.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1605+4936_1605+493 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713809 | |||||
chr16:27713809
|
CATAT | C | 8 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 8 | HG01109.hp1 HG02056.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1605+4934_1605+493 others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713809 | |||||
chr16:27713809
|
CATATAT | C | 7 | a0001c0001t0004g0081a0001c0001t0006g0037a0001c0008t0004g0026others(4): Show | 7 | HG02109.hp1 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1605+4932_1605+493 others(10): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713809 | |||||
chr16:27713809
|
CATATATA others(1): Show |
C | 2 | a0001c0001t0001g0020a0001c0004t0001g0042 | 2 | HG00099.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1605+4930_1605+493 others(12): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713809 | |||||
chr16:27713809
|
CATATATA others(3): Show |
C | 1 | a0001c0001t0001g0006 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1605+4928_1605+493 others(14): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713809 | |||||
chr16:27713809
|
CATATATA others(5): Show |
C | 2 | a0001c0001t0001g0010a0001c0001t0001g0054 | 2 | NA18962.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1605+4926_1605+493 others(16): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713809 | |||||
chr16:27713809
|
CATATATA others(9): Show |
C | 1 | a0001c0001t0001g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1605+4922_1605+493 others(20): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713809 | |||||
chr16:27713809
|
CATATATA others(15): Show |
C | 1 | a0001c0001t0004g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1605+4916_1605+493 others(26): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713809 | |||||
chr16:27713810
|
A | G | 4 | a0001c0012t0002g0137a0001c0028t0004g0109a0003c0003t0002g0128others(1): Show | 4 | HG00099.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1605+4890A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713810 | ||||||
chr16:27713811
|
T | C | 34 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(31): Show | 34 | HG02074.hp1 HG02145.hp1 HG02258.hp2 others(31): Show |
intron_variant | MODIFIER | c.1605+4891T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713811 | ||||||
chr16:27713812
|
A | ACATATTA others(166): Show |
1 | a0011c0017t0005g0151 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1605+4892_1605+489 others(177): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713812 | ||||||
chr16:27713812
|
A | G | 3 | a0001c0018t0011g0122a0004c0030t0005g0115a0011c0017t0005g0150 | 3 | HG01106.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1605+4892A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713812 | ||||||
chr16:27713813
|
T | C | 4 | a0003c0003t0001g0127a0003c0003t0002g0123a0003c0003t0002g0139others(1): Show | 4 | HG01261.hp2 HG01358.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1605+4893T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713813 | ||||||
chr16:27713814
|
A | ACATATTA others(199): Show |
2 | a0002c0002t0003g0067a0002c0002t0003g0072 | 2 | NA18950.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1605+4894_1605+489 others(210): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713814 | ||||||
chr16:27713814
|
A | ACATATTA others(240): Show |
3 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118 | 3 | HG02922.hp2 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1605+4894_1605+489 others(251): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713814 | ||||||
chr16:27713814
|
A | G | 5 | a0001c0004t0001g0138a0001c0018t0011g0122a0003c0003t0002g0120others(2): Show | 5 | HG00140.hp1 HG01106.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1605+4894A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713814 | ||||||
chr16:27713815
|
T | C | 28 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(25): Show | 28 | HG02074.hp1 HG02145.hp1 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1605+4895T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713815 | ||||||
chr16:27713816
|
A | G | 9 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(6): Show | 9 | HG00140.hp1 HG01106.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1605+4896A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713816 | ||||||
chr16:27713817
|
T | C | 2 | a0001c0001t0008g0050a0001c0012t0002g0137 | 2 | HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1605+4897T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713817 | ||||||
chr16:27713817
|
TA | T | 3 | a0003c0003t0001g0127a0003c0003t0002g0123a0003c0003t0002g0139 | 3 | HG01261.hp2 HG01358.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1605+4898delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713817 | ||||||
chr16:27713818
|
A | AC | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1605+4898_1605+489 others(5): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713818 | ||||||
chr16:27713818
|
A | AT | 3 | a0002c0002t0003g0066a0002c0002t0003g0104a0002c0029t0003g0101 | 3 | HG02074.hp1 HG02622.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1605+4899dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713818 | |||||
chr16:27713818
|
A | ATTATATA others(228): Show |
1 | a0002c0002t0003g0098 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1605+4899_1605+490 others(239): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713818 | |||||
chr16:27713818
|
A | ATTATATA others(197): Show |
1 | a0010c0013t0003g0103 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1605+4899_1605+490 others(208): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713818 | |||||
chr16:27713818
|
A | G | 4 | a0001c0018t0011g0122a0002c0002t0003g0062a0008c0016t0001g0077others(1): Show | 4 | HG01106.hp1 HG02132.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1605+4898A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713818 | ||||||
chr16:27713819
|
TA | T | 18 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(15): Show | 18 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1605+4900delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713819 | ||||||
chr16:27713820
|
A | G | 14 | a0001c0024t0001g0078a0002c0002t0003g0062a0002c0002t0003g0063others(11): Show | 14 | HG00408.hp1 HG02132.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.1605+4900A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713820 | ||||||
chr16:27713821
|
T | C | 1 | a0001c0004t0001g0138 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1605+4901T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713821 | ||||||
chr16:27713822
|
A | G | 9 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1605+4902A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713822 | ||||||
chr16:27713823
|
T | C | 7 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(4): Show | 7 | HG02922.hp2 HG03130.hp2 NA18906.hp2 others(4): Show |
intron_variant | MODIFIER | c.1605+4903T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713823 | ||||||
chr16:27713824
|
A | G | 17 | a0003c0003t0002g0094a0003c0003t0002g0121a0003c0003t0002g0125others(14): Show | 17 | HG01258.hp2 HG01361.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.1605+4904A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713824 | ||||||
chr16:27713825
|
T | C | 3 | a0002c0002t0003g0098a0010c0013t0003g0061a0010c0013t0003g0103 | 3 | NA18959.hp2 NA19000.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1605+4905T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713825 | ||||||
chr16:27713826
|
A | ATGTGTGT others(1): Show |
3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1605+4907_1605+490 others(12): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713826 | |||||
chr16:27713826
|
A | ATGTGTGT others(157): Show |
1 | a0003c0003t0002g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1605+4907_1605+490 others(168): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713826 | |||||
chr16:27713826
|
A | ATGTGTGT others(118): Show |
1 | a0003c0003t0002g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1605+4907_1605+490 others(129): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713826 | |||||
chr16:27713826
|
A | ATGTGTGT others(120): Show |
1 | a0003c0003t0001g0127 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1605+4907_1605+490 others(131): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713826 | |||||
chr16:27713826
|
A | ATGTGTGT others(225): Show |
3 | a0007c0010t0002g0112a0007c0010t0002g0113a0007c0010t0002g0114 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1605+4907_1605+490 others(236): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713826 | |||||
chr16:27713826
|
A | ATGTGTGT others(227): Show |
6 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(3): Show | 6 | HG02970.hp1 HG03098.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1605+4907_1605+490 others(238): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713826 | |||||
chr16:27713826
|
A | G | 16 | a0003c0003t0002g0094a0003c0003t0002g0121a0003c0003t0002g0125others(13): Show | 16 | HG01258.hp2 HG01361.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.1605+4906A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713826 | ||||||
chr16:27713827
|
T | C | 7 | a0001c0024t0001g0078a0002c0002t0003g0062a0002c0002t0003g0063others(4): Show | 7 | HG00408.hp1 HG02132.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1605+4907T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713827 | ||||||
chr16:27713827
|
T | TGTGTATA others(194): Show |
1 | a0002c0002t0003g0066 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1605+4907_1605+490 others(205): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713827 | ||||||
chr16:27713827
|
T | TGTGTATA others(196): Show |
1 | a0002c0002t0003g0104 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1605+4907_1605+490 others(207): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713827 | ||||||
chr16:27713828
|
A | ATGTGTGT others(76): Show |
9 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(6): Show | 9 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1605+4909_1605+491 others(87): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713828 | |||||
chr16:27713828
|
A | G | 13 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(10): Show | 13 | HG02622.hp2 HG02886.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.1605+4908A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713828 | ||||||
chr16:27713830
|
A | ATACACAT others(141): Show |
1 | a0004c0034t0005g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1605+4912_1605+491 others(152): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713830 | |||||
chr16:27713830
|
A | ATGTATGT others(152): Show |
1 | a0001c0001t0002g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1605+4911_1605+491 others(163): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713830 | |||||
chr16:27713830
|
A | G | 13 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(10): Show | 13 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1605+4910A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713830 | ||||||
chr16:27713832
|
A | G | 1 | a0013c0027t0001g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1605+4912A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713832 | ||||||
chr16:27713834
|
A | ATACACAT others(139): Show |
3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1605+4916_1605+491 others(150): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713834 | |||||
chr16:27713834
|
A | G | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1605+4914A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713834 | ||||||
chr16:27713837
|
T | C | 10 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(7): Show | 10 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1605+4917T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713837 | ||||||
chr16:27713839
|
T | C | 1 | a0013c0027t0001g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1605+4919T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713839 | ||||||
chr16:27713841
|
T | C | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1605+4921T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713841 | ||||||
chr16:27713841
|
T | TACACATA others(30): Show |
1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1605+4922_1605+492 others(41): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713841 | |||||
chr16:27713846
|
A | C | 1 | a0002c0002t0003g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1605+4926A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713846 | ||||||
chr16:27713846
|
ATATATAT others(5): Show |
A | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1605+4930_1605+494 others(16): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713846 | |||||
chr16:27713850
|
A | C | 9 | a0001c0001t0004g0081a0001c0001t0006g0037a0001c0004t0001g0132others(6): Show | 9 | HG02109.hp1 HG02572.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1605+4930A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713850 | ||||||
chr16:27713854
|
A | ATC | 5 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0083others(2): Show | 5 | HG00741.hp1 HG01358.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1605+4935_1605+493 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713854 | |||||
chr16:27713854
|
A | C | 19 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0004g0024others(16): Show | 19 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1605+4934A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713854 | ||||||
chr16:27713854
|
ATATC | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0057a0015c0020t0004g0008 | 3 | HG00140.hp2 HG01515.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1605+4940_1605+494 others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27713854 | |||||
chr16:27713858
|
C | A | 44 | a0001c0001t0001g0039a0001c0001t0001g0090a0001c0001t0004g0056others(41): Show | 44 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.1605+4938C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27713858 | ||||||
chr16:27714167
|
A | G | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1605+5247A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27714167 | ||||||
chr16:27714330
|
A | G | 16 | a0001c0024t0001g0078a0002c0002t0003g0062a0002c0002t0003g0063others(13): Show | 16 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.1605+5410A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27714330 | ||||||
chr16:27714353
|
G | A | 1 | a0015c0020t0004g0008 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1605+5433G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27714353 | ||||||
chr16:27714543
|
G | A | 13 | a0003c0003t0001g0127a0003c0003t0002g0094a0003c0003t0002g0120others(10): Show | 13 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1605+5623G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27714543 | ||||||
chr16:27714611
|
A | G | 4 | a0001c0004t0001g0132a0002c0002t0003g0134a0002c0002t0003g0135others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1605+5691A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27714611 | ||||||
chr16:27715327
|
C | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1606-6231C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27715327 | ||||||
chr16:27715676
|
G | A | 2 | a0003c0003t0002g0123a0003c0003t0002g0139 | 2 | HG01358.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1606-5882G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27715676 | ||||||
chr16:27715830
|
T | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1606-5728T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27715830 | ||||||
chr16:27715862
|
C | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1606-5696C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27715862 | ||||||
chr16:27715976
|
TA | T | 6 | a0001c0001t0001g0038a0001c0001t0001g0054a0002c0029t0003g0101others(3): Show | 6 | HG02486.hp1 HG02622.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1606-5568delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27715976 | |||||
chr16:27715976
|
TAA | T | 37 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1606-5569_1606-556 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27715976 | |||||
chr16:27716001
|
C | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1606-5557C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27716001 | ||||||
chr16:27716458
|
A | G | 74 | a0001c0001t0002g0071a0001c0004t0001g0042a0001c0004t0001g0116others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(71): Show |
intron_variant | MODIFIER | c.1606-5100A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27716458 | ||||||
chr16:27716539
|
A | G | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1606-5019A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27716539 | ||||||
chr16:27716785
|
G | C | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1606-4773G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27716785 | ||||||
chr16:27716851
|
A | AT | 43 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.1606-4696dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27716851 | |||||
chr16:27716879
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1606-4679C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27716879 | ||||||
chr16:27716943
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1606-4615C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27716943 | ||||||
chr16:27716970
|
A | G | 42 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1606-4588A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27716970 | ||||||
chr16:27717004
|
C | T | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1606-4554C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27717004 | ||||||
chr16:27717133
|
C | T | 1 | a0005c0006t0001g0058 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1606-4425C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27717133 | ||||||
chr16:27717537
|
A | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1606-4021A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27717537 | ||||||
chr16:27717591
|
G | T | 1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1606-3967G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27717591 | ||||||
chr16:27717638
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1606-3920T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27717638 | ||||||
chr16:27718203
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0057 | 2 | HG00140.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1606-3355C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27718203 | ||||||
chr16:27718230
|
C | T | 2 | a0003c0003t0002g0130a0003c0003t0002g0131 | 2 | HG01258.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1606-3328C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27718230 | ||||||
chr16:27718283
|
C | T | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1606-3275C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27718283 | ||||||
chr16:27718617
|
A | T | 2 | a0001c0001t0001g0015a0001c0001t0009g0055 | 2 | HG02165.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1606-2941A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27718617 | ||||||
chr16:27718752
|
CTGCCCAG others(33): Show |
C | 7 | a0005c0006t0001g0013a0005c0006t0001g0058a0005c0006t0001g0059others(4): Show | 7 | HG00741.hp2 HG01243.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1606-2801_1606-276 others(44): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27718752 | |||||
chr16:27719008
|
C | T | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1606-2550C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27719008 | ||||||
chr16:27719384
|
T | C | 1 | a0002c0002t0003g0072 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1606-2174T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27719384 | ||||||
chr16:27719688
|
CT | C | 8 | a0001c0001t0001g0054a0001c0001t0002g0071a0001c0001t0004g0081others(5): Show | 8 | HG02109.hp1 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1606-1854delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27719688 | |||||
chr16:27719982
|
A | G | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1606-1576A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27719982 | ||||||
chr16:27720190
|
A | C | 1 | a0001c0001t0001g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1606-1368A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27720190 | ||||||
chr16:27720208
|
C | T | 1 | a0011c0017t0005g0151 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1606-1350C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27720208 | ||||||
chr16:27720271
|
A | G | 1 | a0013c0027t0001g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1606-1287A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27720271 | ||||||
chr16:27720496
|
C | CT | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(80): Show | 83 | HG00140.hp2 HG00408.hp2 HG00741.hp2 others(80): Show |
intron_variant | MODIFIER | c.1606-1043dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27720496 | |||||
chr16:27720496
|
C | CTT | 28 | a0001c0001t0001g0082a0001c0005t0001g0144a0001c0005t0001g0145others(25): Show | 28 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1606-1044_1606-104 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27720496 | |||||
chr16:27720496
|
CTTTTT | C | 13 | a0003c0003t0001g0127a0003c0003t0002g0094a0003c0003t0002g0120others(10): Show | 13 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1606-1047_1606-104 others(9): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr16 | 27720496 | |||||
chr16:27720737
|
T | C | 1 | a0001c0011t0002g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1606-821T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27720737 | ||||||
chr16:27720825
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1606-733C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27720825 | ||||||
chr16:27721049
|
C | G | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1606-509C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27721049 | ||||||
chr16:27721065
|
G | A | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1606-493G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27721065 | ||||||
chr16:27721073
|
C | T | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1606-485C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27721073 | ||||||
chr16:27721175
|
T | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1606-383T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27721175 | ||||||
chr16:27721340
|
A | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1606-218A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27721340 | ||||||
chr16:27721379
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1606-179G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27721379 | ||||||
chr16:27721490
|
G | A | 9 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(6): Show | 9 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1606-68G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 13/27 | chr16 | 27721490 | ||||||
chr16:27721905
|
T | C | 1 | a0001c0001t0004g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1743+210T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27721905 | ||||||
chr16:27722035
|
C | T | 40 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.1743+340C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27722035 | ||||||
chr16:27722108
|
C | T | 101 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0053others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.1743+413C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27722108 | ||||||
chr16:27722215
|
C | T | 1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1743+520C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27722215 | ||||||
chr16:27722336
|
G | C | 35 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.1743+641G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27722336 | ||||||
chr16:27722394
|
C | T | 17 | a0001c0011t0002g0141a0001c0011t0002g0152a0001c0028t0004g0109others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1743+699C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27722394 | ||||||
chr16:27722399
|
G | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1743+704G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27722399 | ||||||
chr16:27722630
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1743+935G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27722630 | ||||||
chr16:27722641
|
A | T | 3 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0052 | 3 | HG02055.hp1 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1743+946A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27722641 | ||||||
chr16:27723010
|
T | G | 2 | a0001c0001t0001g0053a0001c0001t0004g0017 | 2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1743+1315T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27723010 | ||||||
chr16:27723445
|
G | T | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1743+1750G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27723445 | ||||||
chr16:27723805
|
T | TCCTC | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1743+2124_1743+212 others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27723805 | |||||
chr16:27723819
|
C | CTCCA | 17 | a0001c0004t0001g0042a0001c0024t0001g0078a0002c0002t0003g0062others(14): Show | 17 | HG00099.hp2 HG00408.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1743+2127_1743+212 others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27723819 | |||||
chr16:27723929
|
G | A | 9 | a0001c0004t0001g0132a0004c0007t0001g0074a0004c0007t0001g0075others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1743+2234G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27723929 | ||||||
chr16:27723975
|
C | T | 2 | a0001c0012t0002g0137a0001c0012t0002g0143 | 2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1743+2280C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27723975 | ||||||
chr16:27724101
|
C | T | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1743+2406C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27724101 | ||||||
chr16:27724342
|
G | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1743+2647G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27724342 | ||||||
chr16:27724597
|
C | G | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1743+2902C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27724597 | ||||||
chr16:27724759
|
T | A | 1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1743+3064T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27724759 | ||||||
chr16:27724994
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1743+3299C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27724994 | ||||||
chr16:27725008
|
T | G | 42 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1743+3313T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27725008 | ||||||
chr16:27725871
|
C | CAGGGTAT others(5): Show |
3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1743+4178_1743+418 others(16): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27725871 | |||||
chr16:27725923
|
G | A | 40 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.1743+4228G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27725923 | ||||||
chr16:27726160
|
C | G | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1743+4465C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27726160 | ||||||
chr16:27726195
|
T | C | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1743+4500T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27726195 | ||||||
chr16:27726314
|
C | T | 1 | a0004c0007t0001g0075 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1743+4619C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27726314 | ||||||
chr16:27726331
|
G | A | 3 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146 | 3 | HG02970.hp1 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1743+4636G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27726331 | ||||||
chr16:27726422
|
T | C | 17 | a0001c0004t0001g0042a0001c0024t0001g0078a0002c0002t0003g0062others(14): Show | 17 | HG00099.hp2 HG00408.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1743+4727T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27726422 | ||||||
chr16:27726691
|
G | A | 13 | a0003c0003t0001g0127a0003c0003t0002g0094a0003c0003t0002g0120others(10): Show | 13 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1743+4996G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27726691 | ||||||
chr16:27726864
|
G | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1743+5169G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27726864 | ||||||
chr16:27726947
|
C | T | 1 | a0001c0001t0004g0056 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1743+5252C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27726947 | ||||||
chr16:27726953
|
C | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1743+5258C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27726953 | ||||||
chr16:27727180
|
A | ATGTTTGT others(1): Show |
4 | a0001c0004t0001g0132a0002c0002t0003g0134a0002c0002t0003g0135others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1743+5503_1743+551 others(12): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27727180 | |||||
chr16:27727353
|
A | G | 1 | a0003c0003t0002g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1743+5658A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27727353 | ||||||
chr16:27727931
|
ATAAT | A | 40 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.1743+6243_1743+624 others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27727931 | |||||
chr16:27728063
|
C | CA | 13 | a0001c0001t0001g0053a0001c0001t0002g0040a0001c0001t0004g0017others(10): Show | 13 | HG02055.hp1 HG02109.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1743+6371dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27728063 | |||||
chr16:27728148
|
C | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1743+6453C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27728148 | ||||||
chr16:27728291
|
G | C | 35 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.1743+6596G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27728291 | ||||||
chr16:27728721
|
C | T | 1 | a0001c0001t0004g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1743+7026C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27728721 | ||||||
chr16:27728848
|
T | C | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1743+7153T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27728848 | ||||||
chr16:27729099
|
T | C | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1743+7404T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27729099 | ||||||
chr16:27729340
|
G | A | 42 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1743+7645G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27729340 | ||||||
chr16:27729388
|
C | T | 1 | a0001c0012t0002g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1743+7693C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27729388 | ||||||
chr16:27729759
|
G | A | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1743+8064G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27729759 | ||||||
chr16:27729915
|
C | T | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1743+8220C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27729915 | ||||||
chr16:27729950
|
C | G | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG00408.hp2 HG01978.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1743+8255C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27729950 | ||||||
chr16:27730068
|
C | T | 1 | a0003c0003t0002g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1743+8373C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27730068 | ||||||
chr16:27730235
|
G | A | 35 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.1743+8540G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27730235 | ||||||
chr16:27730312
|
A | G | 1 | a0003c0003t0002g0125 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1743+8617A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27730312 | ||||||
chr16:27730563
|
C | A | 1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1743+8868C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27730563 | ||||||
chr16:27730570
|
C | T | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1743+8875C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27730570 | ||||||
chr16:27730827
|
A | G | 1 | a0005c0006t0001g0059 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1743+9132A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27730827 | ||||||
chr16:27730940
|
C | G | 3 | a0001c0012t0002g0137a0001c0012t0002g0143a0014c0019t0003g0100 | 3 | HG02109.hp2 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1744-9101C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27730940 | ||||||
chr16:27731120
|
AC | A | 9 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(6): Show | 9 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1744-8914delC | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27731120 | |||||
chr16:27731292
|
C | G | 1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1744-8749C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27731292 | ||||||
chr16:27731340
|
G | A | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1744-8701G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27731340 | ||||||
chr16:27731526
|
G | A | 1 | a0001c0024t0001g0078 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1744-8515G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27731526 | ||||||
chr16:27731912
|
C | T | 35 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.1744-8129C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27731912 | ||||||
chr16:27731947
|
G | A | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1744-8094G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27731947 | ||||||
chr16:27732006
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1744-8035G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27732006 | ||||||
chr16:27732167
|
G | A | 35 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.1744-7874G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27732167 | ||||||
chr16:27732377
|
A | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1744-7664A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27732377 | ||||||
chr16:27732540
|
G | A | 1 | a0017c0021t0001g0016 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1744-7501G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27732540 | ||||||
chr16:27732704
|
C | A | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1744-7337C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27732704 | ||||||
chr16:27732731
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1744-7310C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27732731 | ||||||
chr16:27733031
|
C | G | 1 | a0001c0001t0001g0038 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1744-7010C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27733031 | ||||||
chr16:27733128
|
T | C | 1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1744-6913T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27733128 | ||||||
chr16:27733199
|
C | T | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1744-6842C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27733199 | ||||||
chr16:27733564
|
G | GAC | 6 | a0001c0001t0001g0054a0001c0028t0004g0109a0004c0034t0005g0119others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1744-6439_1744-643 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27733564 | |||||
chr16:27733564
|
GAC | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(73): Show | 76 | HG00408.hp2 HG00741.hp1 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.1744-6439_1744-643 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27733564 | |||||
chr16:27733564
|
GACAC | G | 9 | a0001c0001t0004g0056a0001c0004t0001g0116a0001c0004t0001g0118others(6): Show | 9 | HG00140.hp1 HG01106.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1744-6441_1744-643 others(8): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27733564 | |||||
chr16:27733564
|
GACACAC | G | 6 | a0001c0001t0002g0033a0001c0004t0002g0073a0001c0011t0002g0141others(3): Show | 6 | HG01243.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1744-6443_1744-643 others(10): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27733564 | |||||
chr16:27733564
|
GACACACA others(1): Show |
G | 18 | a0001c0001t0001g0015a0001c0001t0009g0055a0001c0004t0001g0117others(15): Show | 18 | HG00099.hp1 HG01109.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1744-6445_1744-643 others(12): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27733564 | |||||
chr16:27733564
|
GACACACA others(7): Show |
G | 2 | a0001c0001t0004g0049a0002c0002t0003g0102 | 2 | HG02630.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1744-6451_1744-643 others(18): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27733564 | |||||
chr16:27733564
|
GACACACA others(9): Show |
G | 16 | a0001c0004t0001g0042a0001c0024t0001g0078a0002c0002t0003g0062others(13): Show | 16 | HG00099.hp2 HG00408.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1744-6453_1744-643 others(20): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27733564 | |||||
chr16:27733674
|
A | G | 5 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1744-6367A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27733674 | ||||||
chr16:27733706
|
GAGCCTGG others(6): Show |
G | 1 | a0001c0001t0001g0007 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1744-6330_1744-631 others(17): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27733706 | |||||
chr16:27733737
|
G | A | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1744-6304G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27733737 | ||||||
chr16:27733785
|
G | C | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1744-6256G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27733785 | ||||||
chr16:27733820
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG01358.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1744-6221C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27733820 | ||||||
chr16:27733832
|
G | T | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1744-6209G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27733832 | ||||||
chr16:27733837
|
G | A | 1 | a0006c0009t0001g0096 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1744-6204G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27733837 | ||||||
chr16:27733939
|
C | T | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1744-6102C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27733939 | ||||||
chr16:27733956
|
T | C | 2 | a0009c0014t0001g0018a0009c0014t0001g0043 | 2 | HG01243.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1744-6085T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27733956 | ||||||
chr16:27734065
|
G | T | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1744-5976G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27734065 | ||||||
chr16:27734299
|
T | G | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1744-5742T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27734299 | ||||||
chr16:27734365
|
G | C | 3 | a0001c0012t0002g0137a0001c0012t0002g0143a0014c0019t0003g0100 | 3 | HG02109.hp2 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1744-5676G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27734365 | ||||||
chr16:27734395
|
T | TA | 8 | a0001c0001t0001g0039a0001c0001t0001g0047a0001c0001t0001g0082others(5): Show | 8 | HG01109.hp1 HG01517.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1744-5625dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27734395 | |||||
chr16:27734395
|
TA | T | 39 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1744-5625delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27734395 | |||||
chr16:27734519
|
T | C | 17 | a0001c0004t0001g0042a0001c0024t0001g0078a0002c0002t0003g0062others(14): Show | 17 | HG00099.hp2 HG00408.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1744-5522T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27734519 | ||||||
chr16:27734550
|
A | T | 1 | a0001c0001t0001g0031 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1744-5491A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27734550 | ||||||
chr16:27734753
|
G | C | 5 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1744-5288G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27734753 | ||||||
chr16:27734935
|
A | C | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1744-5106A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27734935 | ||||||
chr16:27735170
|
A | T | 1 | a0001c0001t0002g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1744-4871A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27735170 | ||||||
chr16:27735219
|
C | T | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1744-4822C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27735219 | ||||||
chr16:27735337
|
A | G | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1744-4704A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27735337 | ||||||
chr16:27736158
|
A | G | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1744-3883A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27736158 | ||||||
chr16:27736372
|
C | G | 3 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146 | 3 | HG02970.hp1 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1744-3669C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27736372 | ||||||
chr16:27736736
|
C | T | 35 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.1744-3305C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27736736 | ||||||
chr16:27736982
|
A | AGAGGGGA others(1): Show |
42 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1744-3049_1744-304 others(12): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27736982 | |||||
chr16:27737047
|
G | A | 6 | a0001c0001t0004g0081a0001c0001t0006g0037a0001c0008t0004g0026others(3): Show | 6 | HG02109.hp1 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1744-2994G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27737047 | ||||||
chr16:27737107
|
T | C | 35 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.1744-2934T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27737107 | ||||||
chr16:27737188
|
G | C | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1744-2853G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27737188 | ||||||
chr16:27737354
|
G | T | 1 | a0001c0001t0001g0082 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1744-2687G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27737354 | ||||||
chr16:27737355
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1744-2686C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27737355 | ||||||
chr16:27737399
|
G | C | 1 | a0001c0001t0004g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1744-2642G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27737399 | ||||||
chr16:27737422
|
A | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1744-2619A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27737422 | ||||||
chr16:27737496
|
G | A | 2 | a0001c0015t0001g0012a0001c0015t0001g0084 | 2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1744-2545G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27737496 | ||||||
chr16:27737507
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1744-2534A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27737507 | ||||||
chr16:27737534
|
C | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1744-2507C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27737534 | ||||||
chr16:27737586
|
G | A | 1 | a0004c0030t0005g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1744-2455G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27737586 | ||||||
chr16:27737597
|
G | A | 1 | a0004c0030t0005g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1744-2444G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27737597 | ||||||
chr16:27737757
|
C | T | 3 | a0001c0012t0002g0137a0001c0012t0002g0143a0014c0019t0003g0100 | 3 | HG02109.hp2 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1744-2284C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27737757 | ||||||
chr16:27737786
|
C | T | 1 | a0001c0024t0001g0078 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1744-2255C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27737786 | ||||||
chr16:27737867
|
CAG | C | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1744-2172_1744-217 others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27737867 | |||||
chr16:27737930
|
C | T | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1744-2111C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27737930 | ||||||
chr16:27737955
|
G | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1744-2086G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27737955 | ||||||
chr16:27738422
|
G | T | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1744-1619G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27738422 | ||||||
chr16:27738541
|
A | C | 17 | a0001c0004t0001g0042a0001c0024t0001g0078a0002c0002t0003g0062others(14): Show | 17 | HG00099.hp2 HG00408.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1744-1500A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27738541 | ||||||
chr16:27738662
|
G | T | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1744-1379G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27738662 | ||||||
chr16:27738828
|
T | C | 1 | a0001c0015t0001g0084 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1744-1213T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27738828 | ||||||
chr16:27738952
|
A | C | 6 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(3): Show | 6 | HG02970.hp1 HG03098.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1744-1089A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27738952 | ||||||
chr16:27739006
|
TA | T | 44 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(41): Show | 44 | HG00099.hp1 HG00140.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.1744-1022delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr16 | 27739006 | |||||
chr16:27739105
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1744-936C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27739105 | ||||||
chr16:27739123
|
T | C | 41 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.1744-918T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27739123 | ||||||
chr16:27739684
|
G | T | 1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1744-357G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27739684 | ||||||
chr16:27739777
|
G | A | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1744-264G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27739777 | ||||||
chr16:27739810
|
C | T | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1744-231C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27739810 | ||||||
chr16:27739812
|
G | A | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1744-229G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27739812 | ||||||
chr16:27739823
|
C | T | 3 | a0007c0010t0002g0112a0007c0010t0002g0113a0007c0010t0002g0114 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1744-218C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 14/27 | chr16 | 27739823 | ||||||
chr16:27740976
|
G | T | 1 | a0001c0001t0002g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2623+56G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27740976 | ||||||
chr16:27740993
|
T | TC | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.2623+75dupC | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr16 | 27740993 | |||||
chr16:27741420
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2623+500A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27741420 | ||||||
chr16:27741486
|
A | G | 35 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2623+566A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27741486 | ||||||
chr16:27741571
|
G | A | 2 | a0001c0001t0001g0093a0004c0030t0005g0115 | 2 | HG00741.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2623+651G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27741571 | ||||||
chr16:27741896
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2623+976C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27741896 | ||||||
chr16:27741943
|
T | C | 42 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.2623+1023T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27741943 | ||||||
chr16:27741949
|
C | G | 1 | a0001c0001t0001g0023 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2623+1029C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27741949 | ||||||
chr16:27742032
|
C | CA | 23 | a0001c0001t0001g0006a0001c0001t0001g0047a0001c0001t0001g0054others(20): Show | 23 | HG00408.hp1 HG01109.hp1 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.2623+1128dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr16 | 27742032 | |||||
chr16:27742181
|
G | A | 1 | a0002c0002t0003g0065 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2623+1261G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27742181 | ||||||
chr16:27742184
|
T | C | 1 | a0001c0008t0004g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2623+1264T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27742184 | ||||||
chr16:27742305
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2623+1385G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27742305 | ||||||
chr16:27742336
|
G | A | 7 | a0003c0003t0001g0127a0003c0003t0002g0125a0003c0003t0002g0126others(4): Show | 7 | HG01258.hp2 HG01261.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.2623+1416G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27742336 | ||||||
chr16:27742416
|
G | A | 13 | a0003c0003t0001g0127a0003c0003t0002g0094a0003c0003t0002g0120others(10): Show | 13 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2623+1496G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27742416 | ||||||
chr16:27742470
|
C | T | 1 | a0001c0012t0002g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2623+1550C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27742470 | ||||||
chr16:27742499
|
C | T | 2 | a0010c0013t0003g0061a0010c0013t0003g0103 | 2 | NA19000.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2623+1579C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27742499 | ||||||
chr16:27742565
|
G | A | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2623+1645G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27742565 | ||||||
chr16:27742851
|
C | CTTTTT | 74 | a0001c0001t0002g0071a0001c0004t0001g0042a0001c0004t0001g0116others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(71): Show |
intron_variant | MODIFIER | c.2623+1934_2623+193 others(9): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr16 | 27742851 | |||||
chr16:27742872
|
C | T | 1 | a0001c0001t0001g0006 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2623+1952C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27742872 | ||||||
chr16:27742884
|
T | C | 3 | a0001c0012t0002g0137a0001c0012t0002g0143a0014c0019t0003g0100 | 3 | HG02109.hp2 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2623+1964T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27742884 | ||||||
chr16:27743067
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2623+2147T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27743067 | ||||||
chr16:27743124
|
T | C | 69 | a0001c0004t0001g0042a0001c0004t0001g0116a0001c0004t0001g0117others(66): Show | 69 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(66): Show |
intron_variant | MODIFIER | c.2623+2204T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27743124 | ||||||
chr16:27743317
|
A | T | 1 | a0001c0001t0001g0093 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2623+2397A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27743317 | ||||||
chr16:27743336
|
G | T | 1 | a0001c0001t0004g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2623+2416G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27743336 | ||||||
chr16:27743904
|
G | A | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2623+2984G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27743904 | ||||||
chr16:27743961
|
A | G | 10 | a0001c0001t0001g0053a0001c0001t0002g0011a0001c0001t0002g0014others(7): Show | 10 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2623+3041A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27743961 | ||||||
chr16:27744072
|
A | G | 17 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(14): Show | 17 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.2623+3152A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27744072 | ||||||
chr16:27744121
|
A | C | 42 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.2623+3201A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27744121 | ||||||
chr16:27744371
|
T | A | 45 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.2623+3451T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27744371 | ||||||
chr16:27744372
|
A | T | 1 | a0001c0001t0002g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2623+3452A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27744372 | ||||||
chr16:27744571
|
G | C | 3 | a0007c0010t0002g0112a0007c0010t0002g0113a0007c0010t0002g0114 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2623+3651G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27744571 | ||||||
chr16:27744608
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2623+3688C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27744608 | ||||||
chr16:27744745
|
T | G | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2623+3825T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27744745 | ||||||
chr16:27744772
|
ACTCGGGA others(25): Show |
A | 1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2623+3894_2623+392 others(36): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr16 | 27744772 | |||||
chr16:27744775
|
C | T | 13 | a0003c0003t0001g0127a0003c0003t0002g0094a0003c0003t0002g0120others(10): Show | 13 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2623+3855C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27744775 | ||||||
chr16:27744840
|
G | A | 2 | a0005c0006t0001g0058a0005c0006t0001g0064 | 2 | NA18971.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2623+3920G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27744840 | ||||||
chr16:27744868
|
T | C | 1 | a0001c0001t0002g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2623+3948T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27744868 | ||||||
chr16:27744927
|
CATAAA | C | 5 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2623+4013_2623+401 others(9): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr16 | 27744927 | |||||
chr16:27744941
|
T | C | 16 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0015others(13): Show | 16 | HG00408.hp2 HG01106.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.2623+4021T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27744941 | ||||||
chr16:27745246
|
T | A | 5 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2623+4326T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27745246 | ||||||
chr16:27745257
|
C | A | 1 | a0004c0034t0005g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2624-4327C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27745257 | ||||||
chr16:27745447
|
A | T | 1 | a0005c0006t0001g0013 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2624-4137A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27745447 | ||||||
chr16:27745545
|
T | G | 45 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.2624-4039T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27745545 | ||||||
chr16:27745580
|
C | T | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2624-4004C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27745580 | ||||||
chr16:27745697
|
C | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2624-3887C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27745697 | ||||||
chr16:27745898
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.2624-3686G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27745898 | ||||||
chr16:27745957
|
C | CT | 32 | a0001c0001t0001g0047a0001c0001t0001g0082a0001c0001t0001g0083others(29): Show | 32 | HG00099.hp2 HG00408.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.2624-3602dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr16 | 27745957 | |||||
chr16:27745957
|
CT | C | 11 | a0001c0001t0001g0006a0001c0001t0002g0071a0004c0007t0001g0074others(8): Show | 11 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2624-3602delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr16 | 27745957 | |||||
chr16:27746125
|
C | T | 1 | a0001c0011t0002g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2624-3459C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27746125 | ||||||
chr16:27746192
|
C | T | 8 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2624-3392C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27746192 | ||||||
chr16:27746267
|
C | T | 32 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.2624-3317C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27746267 | ||||||
chr16:27746387
|
G | A | 3 | a0001c0012t0002g0137a0001c0012t0002g0143a0014c0019t0003g0100 | 3 | HG02109.hp2 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2624-3197G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27746387 | ||||||
chr16:27746775
|
G | A | 5 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2624-2809G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27746775 | ||||||
chr16:27747013
|
C | T | 1 | a0004c0007t0001g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2624-2571C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27747013 | ||||||
chr16:27747119
|
G | A | 3 | a0001c0012t0002g0137a0001c0012t0002g0143a0014c0019t0003g0100 | 3 | HG02109.hp2 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2624-2465G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27747119 | ||||||
chr16:27747421
|
G | A | 2 | a0003c0003t0002g0126a0003c0003t0002g0129 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2624-2163G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27747421 | ||||||
chr16:27747843
|
C | T | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2624-1741C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27747843 | ||||||
chr16:27747852
|
G | A | 2 | a0001c0012t0002g0137a0001c0012t0002g0143 | 2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2624-1732G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27747852 | ||||||
chr16:27748135
|
T | G | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2624-1449T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27748135 | ||||||
chr16:27748220
|
C | T | 1 | a0003c0003t0002g0128 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2624-1364C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27748220 | ||||||
chr16:27748356
|
C | T | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2624-1228C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27748356 | ||||||
chr16:27748507
|
C | T | 31 | a0001c0001t0002g0071a0001c0004t0001g0116a0001c0004t0001g0117others(28): Show | 31 | HG00408.hp1 HG01109.hp2 HG02074.hp1 others(28): Show |
intron_variant | MODIFIER | c.2624-1077C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27748507 | ||||||
chr16:27748658
|
T | C | 4 | a0001c0012t0002g0137a0001c0012t0002g0143a0013c0027t0001g0004others(1): Show | 4 | HG02109.hp2 HG02630.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2624-926T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27748658 | ||||||
chr16:27748681
|
G | A | 4 | a0001c0001t0008g0050a0001c0012t0002g0137a0001c0012t0002g0143others(1): Show | 4 | HG02109.hp2 HG02630.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2624-903G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27748681 | ||||||
chr16:27749139
|
C | T | 16 | a0001c0024t0001g0078a0002c0002t0003g0062a0002c0002t0003g0063others(13): Show | 16 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.2624-445C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27749139 | ||||||
chr16:27749201
|
A | C | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2624-383A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27749201 | ||||||
chr16:27749235
|
T | C | 38 | a0001c0004t0001g0042a0001c0004t0001g0116a0001c0004t0001g0117others(35): Show | 38 | HG00099.hp2 HG00408.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.2624-349T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27749235 | ||||||
chr16:27749247
|
A | G | 1 | a0001c0005t0002g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2624-337A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27749247 | ||||||
chr16:27749410
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2624-174C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27749410 | ||||||
chr16:27749493
|
T | G | 1 | a0002c0002t0003g0099 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2624-91T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27749493 | ||||||
chr16:27749563
|
C | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0004g0005others(2): Show | 5 | HG01515.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2624-21C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 15/27 | chr16 | 27749563 | ||||||
chr16:27750310
|
T | C | 38 | a0001c0004t0001g0042a0001c0004t0001g0116a0001c0004t0001g0117others(35): Show | 38 | HG00099.hp2 HG00408.hp1 HG01109.hp2 others(35): Show |
splice_region_variant&intron_variant | LOW | c.3346+4T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/27 | chr16 | 27750310 | ||||||
chr16:27750419
|
C | CT | 9 | a0001c0001t0002g0071a0001c0005t0001g0144a0001c0005t0001g0145others(6): Show | 9 | HG01106.hp1 HG02486.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.3346+131dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr16 | 27750419 | |||||
chr16:27750419
|
CT | C | 34 | a0001c0001t0001g0038a0001c0004t0001g0042a0001c0004t0001g0116others(31): Show | 34 | HG00099.hp2 HG00408.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.3346+131delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr16 | 27750419 | |||||
chr16:27750438
|
G | C | 9 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0146others(6): Show | 9 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.3346+132G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/27 | chr16 | 27750438 | ||||||
chr16:27750595
|
A | AT | 8 | a0001c0001t0001g0031a0001c0001t0001g0133a0001c0011t0002g0141others(5): Show | 8 | HG01243.hp2 HG02056.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3346+307dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr16 | 27750595 | |||||
chr16:27750595
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3346+289A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/27 | chr16 | 27750595 | ||||||
chr16:27750659
|
C | A | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3346+353C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/27 | chr16 | 27750659 | ||||||
chr16:27750679
|
G | A | 3 | a0001c0012t0002g0137a0001c0012t0002g0143a0014c0019t0003g0100 | 3 | HG02109.hp2 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3346+373G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/27 | chr16 | 27750679 | ||||||
chr16:27750683
|
C | T | 31 | a0001c0004t0001g0042a0001c0004t0001g0116a0001c0004t0001g0117others(28): Show | 31 | HG00099.hp2 HG00408.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.3346+377C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/27 | chr16 | 27750683 | ||||||
chr16:27750732
|
C | CT | 29 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0028others(26): Show | 29 | HG00741.hp2 HG01106.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.3346+449dupT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr16 | 27750732 | |||||
chr16:27750732
|
CT | C | 17 | a0001c0012t0002g0137a0001c0012t0002g0143a0002c0002t0003g0098others(14): Show | 17 | HG00099.hp1 HG01258.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.3346+449delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr16 | 27750732 | |||||
chr16:27751474
|
C | T | 1 | a0017c0021t0001g0016 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3347-245C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/27 | chr16 | 27751474 | ||||||
chr16:27751492
|
TCA | T | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3347-224_3347-223d others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr16 | 27751492 | |||||
chr16:27751551
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3347-168G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 16/27 | chr16 | 27751551 | ||||||
chr16:27752164
|
C | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3552+240C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27752164 | ||||||
chr16:27752220
|
G | T | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3552+296G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27752220 | ||||||
chr16:27752250
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0022 | 2 | HG01978.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3552+326T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27752250 | ||||||
chr16:27752326
|
G | A | 2 | a0001c0004t0001g0116a0001c0004t0001g0118 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3552+402G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27752326 | ||||||
chr16:27752562
|
T | C | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3552+638T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27752562 | ||||||
chr16:27752642
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3552+718C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27752642 | ||||||
chr16:27752643
|
C | T | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3552+719C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27752643 | ||||||
chr16:27752955
|
G | T | 27 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0053others(24): Show | 27 | HG01515.hp2 HG02055.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.3552+1031G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27752955 | ||||||
chr16:27753097
|
G | C | 3 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0052 | 3 | HG02055.hp1 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3553-1076G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27753097 | ||||||
chr16:27753130
|
G | A | 4 | a0005c0006t0001g0013a0005c0006t0001g0058a0005c0006t0001g0059others(1): Show | 4 | HG02056.hp1 NA18971.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.3553-1043G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27753130 | ||||||
chr16:27753310
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3553-863C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27753310 | ||||||
chr16:27753311
|
G | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3553-862G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27753311 | ||||||
chr16:27753382
|
C | A | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3553-791C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27753382 | ||||||
chr16:27753566
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3553-607T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27753566 | ||||||
chr16:27753712
|
C | CCCTT | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.3553-442_3553-439d others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr16 | 27753712 | |||||
chr16:27753712
|
C | CCCTTCCT others(9): Show |
1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3553-454_3553-439d others(18): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr16 | 27753712 | |||||
chr16:27753731
|
T | TTCCC | 2 | a0009c0014t0001g0018a0009c0014t0001g0043 | 2 | HG01243.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3553-426_3553-423d others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr16 | 27753731 | |||||
chr16:27753783
|
CTCCT | C | 38 | a0001c0004t0001g0042a0001c0004t0001g0116a0001c0004t0001g0117others(35): Show | 38 | HG00099.hp2 HG00408.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.3553-373_3553-370d others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr16 | 27753783 | |||||
chr16:27753874
|
ACATAAGC others(11): Show |
A | 3 | a0001c0012t0002g0137a0001c0012t0002g0143a0014c0019t0003g0100 | 3 | HG02109.hp2 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3553-297_3553-280d others(20): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr16 | 27753874 | |||||
chr16:27753975
|
G | A | 7 | a0004c0007t0001g0074a0004c0007t0001g0075a0004c0007t0001g0105others(4): Show | 7 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3553-198G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27753975 | ||||||
chr16:27753994
|
G | C | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3553-179G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27753994 | ||||||
chr16:27753998
|
C | T | 1 | a0001c0001t0001g0010 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3553-175C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27753998 | ||||||
chr16:27754017
|
A | G | 1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3553-156A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 17/27 | chr16 | 27754017 | ||||||
chr16:27754287
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3631+36G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27754287 | ||||||
chr16:27754443
|
T | C | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3631+192T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27754443 | ||||||
chr16:27754804
|
T | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3631+553T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27754804 | ||||||
chr16:27754893
|
T | C | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3631+642T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27754893 | ||||||
chr16:27755115
|
CT | C | 30 | a0001c0004t0001g0042a0001c0004t0001g0116a0001c0004t0001g0117others(27): Show | 30 | HG00099.hp2 HG00408.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.3631+865delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27755115 | ||||||
chr16:27755553
|
G | A | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3631+1302G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27755553 | ||||||
chr16:27755870
|
T | G | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3631+1619T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27755870 | ||||||
chr16:27755878
|
A | C | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3631+1627A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27755878 | ||||||
chr16:27756063
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG01358.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.3631+1812G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27756063 | ||||||
chr16:27756125
|
G | T | 1 | a0018c0025t0003g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3631+1874G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27756125 | ||||||
chr16:27756223
|
C | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | NA18747.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.3631+1972C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27756223 | ||||||
chr16:27756266
|
C | T | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3631+2015C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27756266 | ||||||
chr16:27756294
|
C | T | 1 | a0002c0002t0003g0063 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3631+2043C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27756294 | ||||||
chr16:27756316
|
C | G | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.3631+2065C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27756316 | ||||||
chr16:27756553
|
G | A | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3631+2302G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27756553 | ||||||
chr16:27756767
|
T | C | 1 | a0001c0001t0001g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3631+2516T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27756767 | ||||||
chr16:27756859
|
C | G | 1 | a0002c0002t0003g0063 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3631+2608C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27756859 | ||||||
chr16:27756891
|
T | C | 2 | a0001c0001t0008g0050a0001c0028t0004g0109 | 2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3631+2640T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27756891 | ||||||
chr16:27757038
|
C | G | 1 | a0001c0001t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3631+2787C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27757038 | ||||||
chr16:27757140
|
A | C | 3 | a0001c0018t0011g0122a0002c0029t0003g0101a0019c0032t0003g0001 | 3 | HG01106.hp1 HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3631+2889A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27757140 | ||||||
chr16:27757197
|
G | A | 3 | a0003c0003t0001g0127a0003c0003t0002g0126a0003c0003t0002g0129 | 3 | HG01261.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3631+2946G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27757197 | ||||||
chr16:27757332
|
C | G | 1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3631+3081C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27757332 | ||||||
chr16:27757380
|
C | T | 2 | a0001c0011t0002g0141a0001c0011t0002g0152 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3631+3129C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27757380 | ||||||
chr16:27757381
|
G | A | 1 | a0004c0007t0001g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3631+3130G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27757381 | ||||||
chr16:27757604
|
A | G | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3631+3353A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27757604 | ||||||
chr16:27757751
|
A | T | 1 | a0001c0001t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3631+3500A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27757751 | ||||||
chr16:27757835
|
T | G | 1 | a0001c0001t0001g0082 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3632-3578T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27757835 | ||||||
chr16:27757861
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3632-3552T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27757861 | ||||||
chr16:27757896
|
AG | A | 2 | a0001c0001t0004g0025a0001c0001t0004g0052 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3632-3516delG | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27757896 | ||||||
chr16:27758202
|
C | T | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3632-3211C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27758202 | ||||||
chr16:27758396
|
A | G | 1 | a0004c0030t0005g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3632-3017A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27758396 | ||||||
chr16:27758573
|
G | A | 21 | a0001c0001t0002g0071a0001c0001t0008g0050a0001c0004t0002g0070others(18): Show | 21 | HG01243.hp2 HG02055.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.3632-2840G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27758573 | ||||||
chr16:27758710
|
A | G | 2 | a0001c0001t0004g0025a0001c0001t0004g0052 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3632-2703A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27758710 | ||||||
chr16:27758796
|
C | G | 12 | a0001c0001t0001g0019a0001c0001t0001g0047a0001c0001t0004g0024others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.3632-2617C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27758796 | ||||||
chr16:27758815
|
A | G | 2 | a0002c0029t0003g0101a0019c0032t0003g0001 | 2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3632-2598A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27758815 | ||||||
chr16:27758879
|
T | A | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3632-2534T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27758879 | ||||||
chr16:27759381
|
A | T | 1 | a0004c0007t0010g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3632-2032A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27759381 | ||||||
chr16:27759492
|
C | T | 70 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.3632-1921C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27759492 | ||||||
chr16:27759531
|
T | C | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3632-1882T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27759531 | ||||||
chr16:27759630
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3632-1783T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27759630 | ||||||
chr16:27760138
|
C | A | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3632-1275C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27760138 | ||||||
chr16:27760219
|
C | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0005t0001g0144others(2): Show | 5 | HG02970.hp1 HG03098.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.3632-1194C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27760219 | ||||||
chr16:27760318
|
T | C | 1 | a0001c0001t0001g0010 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3632-1095T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27760318 | ||||||
chr16:27760586
|
A | G | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3632-827A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27760586 | ||||||
chr16:27760626
|
A | G | 3 | a0001c0001t0001g0053a0001c0001t0004g0017a0001c0001t0004g0051 | 3 | HG02615.hp1 HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3632-787A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27760626 | ||||||
chr16:27760647
|
A | G | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3632-766A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27760647 | ||||||
chr16:27761014
|
C | T | 2 | a0001c0012t0002g0137a0001c0012t0002g0143 | 2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3632-399C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27761014 | ||||||
chr16:27761159
|
C | T | 17 | a0002c0002t0003g0062a0002c0002t0003g0063a0002c0002t0003g0065others(14): Show | 17 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.3632-254C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27761159 | ||||||
chr16:27761168
|
G | T | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3632-245G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27761168 | ||||||
chr16:27761253
|
C | A | 1 | a0005c0006t0001g0085 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3632-160C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 18/27 | chr16 | 27761253 | ||||||
chr16:27761889
|
G | A | 1 | a0001c0012t0002g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3809+299G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27761889 | ||||||
chr16:27761925
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3809+335T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27761925 | ||||||
chr16:27761965
|
C | T | 6 | a0003c0003t0002g0125a0003c0003t0002g0126a0003c0003t0002g0129others(3): Show | 6 | HG01258.hp2 HG01361.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.3809+375C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27761965 | ||||||
chr16:27762100
|
G | A | 11 | a0002c0002t0003g0062a0002c0002t0003g0063a0002c0002t0003g0065others(8): Show | 11 | HG00408.hp1 HG02074.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.3809+510G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27762100 | ||||||
chr16:27762175
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3809+585A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27762175 | ||||||
chr16:27762393
|
T | C | 1 | a0019c0032t0003g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3809+803T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27762393 | ||||||
chr16:27762801
|
A | G | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3809+1211A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27762801 | ||||||
chr16:27762859
|
G | A | 1 | a0001c0001t0004g0056 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3809+1269G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27762859 | ||||||
chr16:27763046
|
A | C | 1 | a0001c0028t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3809+1456A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27763046 | ||||||
chr16:27763225
|
G | T | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3809+1635G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27763225 | ||||||
chr16:27763441
|
T | TA | 39 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0053others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(36): Show |
intron_variant | MODIFIER | c.3809+1877dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr16 | 27763441 | |||||
chr16:27763441
|
TA | T | 31 | a0001c0001t0001g0006a0001c0001t0001g0133a0001c0004t0001g0132others(28): Show | 31 | HG00408.hp1 HG01106.hp1 HG02074.hp1 others(28): Show |
intron_variant | MODIFIER | c.3809+1877delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr16 | 27763441 | |||||
chr16:27763619
|
C | CA | 5 | a0001c0011t0002g0141a0001c0011t0002g0152a0002c0002t0003g0110others(2): Show | 5 | HG01243.hp2 HG02135.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3809+2048dupA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr16 | 27763619 | |||||
chr16:27763619
|
CA | C | 5 | a0001c0008t0004g0041a0004c0030t0005g0115a0004c0034t0005g0119others(2): Show | 5 | HG02145.hp2 HG03041.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3809+2048delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr16 | 27763619 | |||||
chr16:27763832
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3809+2242A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27763832 | ||||||
chr16:27763993
|
G | A | 2 | a0001c0001t0008g0050a0001c0028t0004g0109 | 2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3810-2316G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27763993 | ||||||
chr16:27764603
|
C | A | 73 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(70): Show |
intron_variant | MODIFIER | c.3810-1706C>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27764603 | ||||||
chr16:27764680
|
C | G | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3810-1629C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27764680 | ||||||
chr16:27765030
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3810-1279G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27765030 | ||||||
chr16:27765282
|
G | A | 1 | a0013c0027t0001g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3810-1027G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27765282 | ||||||
chr16:27765484
|
C | T | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3810-825C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27765484 | ||||||
chr16:27765548
|
C | G | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3810-761C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27765548 | ||||||
chr16:27765692
|
C | T | 1 | a0001c0026t0004g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3810-617C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27765692 | ||||||
chr16:27766237
|
G | A | 1 | a0001c0018t0011g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3810-72G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 19/27 | chr16 | 27766237 | ||||||
chr16:27766510
|
A | G | 143 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.3975+36A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 20/27 | chr16 | 27766510 | ||||||
chr16:27766591
|
C | G | 1 | a0001c0001t0001g0010 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3975+117C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 20/27 | chr16 | 27766591 | ||||||
chr16:27766713
|
G | A | 1 | a0004c0007t0010g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3975+239G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 20/27 | chr16 | 27766713 | ||||||
chr16:27766964
|
G | A | 2 | a0001c0012t0002g0137a0001c0012t0002g0143 | 2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3975+490G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 20/27 | chr16 | 27766964 | ||||||
chr16:27766984
|
C | T | 2 | a0014c0019t0003g0100a0018c0025t0003g0111 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3975+510C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 20/27 | chr16 | 27766984 | ||||||
chr16:27767139
|
A | G | 1 | a0001c0001t0004g0056 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3975+665A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 20/27 | chr16 | 27767139 | ||||||
chr16:27767322
|
G | A | 1 | a0005c0006t0001g0059 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.3975+848G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 20/27 | chr16 | 27767322 | ||||||
chr16:27767869
|
C | T | 24 | a0001c0004t0001g0042a0001c0004t0001g0132a0002c0002t0003g0062others(21): Show | 24 | HG00099.hp2 HG00408.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.3975+1395C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 20/27 | chr16 | 27767869 | ||||||
chr16:27767958
|
T | G | 16 | a0001c0004t0001g0042a0002c0002t0003g0062a0002c0002t0003g0063others(13): Show | 16 | HG00099.hp2 HG00408.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.3975+1484T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 20/27 | chr16 | 27767958 | ||||||
chr16:27768108
|
C | T | 2 | a0001c0012t0002g0137a0001c0012t0002g0143 | 2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3975+1634C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 20/27 | chr16 | 27768108 | ||||||
chr16:27768110
|
T | G | 2 | a0001c0012t0002g0137a0001c0012t0002g0143 | 2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3975+1636T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 20/27 | chr16 | 27768110 | ||||||
chr16:27768819
|
G | A | 2 | a0001c0001t0004g0005a0001c0001t0004g0049 | 2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3976-1042G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 20/27 | chr16 | 27768819 | ||||||
chr16:27768858
|
G | T | 29 | a0001c0004t0001g0042a0001c0004t0001g0132a0001c0018t0011g0122others(26): Show | 29 | HG00099.hp2 HG00408.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.3976-1003G>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 20/27 | chr16 | 27768858 | ||||||
chr16:27769057
|
C | T | 89 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0053others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.3976-804C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 20/27 | chr16 | 27769057 | ||||||
chr16:27769206
|
A | C | 25 | a0001c0004t0001g0042a0001c0004t0001g0132a0001c0018t0011g0122others(22): Show | 25 | HG00099.hp2 HG00408.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.3976-655A>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 20/27 | chr16 | 27769206 | ||||||
chr16:27770067
|
C | G | 1 | a0001c0001t0008g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4133+49C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 21/27 | chr16 | 27770067 | ||||||
chr16:27770130
|
A | G | 1 | a0013c0027t0001g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4133+112A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 21/27 | chr16 | 27770130 | ||||||
chr16:27770177
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4133+159G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 21/27 | chr16 | 27770177 | ||||||
chr16:27770264
|
G | A | 1 | a0001c0001t0004g0024 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4133+246G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 21/27 | chr16 | 27770264 | ||||||
chr16:27770488
|
T | C | 16 | a0001c0004t0001g0042a0002c0002t0003g0062a0002c0002t0003g0063others(13): Show | 16 | HG00099.hp2 HG00408.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.4133+470T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 21/27 | chr16 | 27770488 | ||||||
chr16:27770513
|
C | T | 1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4133+495C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 21/27 | chr16 | 27770513 | ||||||
chr16:27770646
|
G | A | 1 | a0001c0015t0001g0084 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4133+628G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 21/27 | chr16 | 27770646 | ||||||
chr16:27770670
|
G | A | 6 | a0003c0003t0002g0094a0003c0003t0002g0120a0003c0003t0002g0121others(3): Show | 6 | HG00099.hp1 HG00140.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.4133+652G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 21/27 | chr16 | 27770670 | ||||||
chr16:27770690
|
G | A | 1 | a0004c0030t0005g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4133+672G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 21/27 | chr16 | 27770690 | ||||||
chr16:27770759
|
C | T | 4 | a0001c0004t0001g0132a0002c0002t0003g0134a0002c0002t0003g0135others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.4133+741C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 21/27 | chr16 | 27770759 | ||||||
chr16:27770806
|
G | A | 1 | a0001c0004t0001g0042 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4134-782G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 21/27 | chr16 | 27770806 | ||||||
chr16:27771013
|
G | A | 1 | a0005c0006t0001g0059 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.4134-575G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 21/27 | chr16 | 27771013 | ||||||
chr16:27771217
|
C | T | 4 | a0001c0004t0001g0132a0002c0002t0003g0134a0002c0002t0003g0135others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.4134-371C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 21/27 | chr16 | 27771217 | ||||||
chr16:27771517
|
C | G | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.4134-71C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 21/27 | chr16 | 27771517 | ||||||
chr16:27771521
|
G | C | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.4134-67G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 21/27 | chr16 | 27771521 | ||||||
chr16:27771694
|
G | A | 1 | a0004c0007t0010g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4198+42G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 22/27 | chr16 | 27771694 | ||||||
chr16:27772057
|
G | A | 1 | a0001c0001t0001g0009 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.4198+405G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 22/27 | chr16 | 27772057 | ||||||
chr16:27772728
|
T | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4199-371T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 22/27 | chr16 | 27772728 | ||||||
chr16:27772851
|
G | A | 5 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.4199-248G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 22/27 | chr16 | 27772851 | ||||||
chr16:27772886
|
CACAT | C | 2 | a0003c0003t0002g0126a0003c0003t0002g0129 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.4199-212_4199-209d others(6): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 22/27 | chr16 | 27772886 | ||||||
chr16:27772891
|
GCA | G | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.4199-193_4199-192d others(4): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr16 | 27772891 | |||||
chr16:27773005
|
T | C | 1 | a0004c0034t0005g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4199-94T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 22/27 | chr16 | 27773005 | ||||||
chr16:27773050
|
T | C | 2 | a0001c0001t0004g0081a0001c0001t0006g0037 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.4199-49T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 22/27 | chr16 | 27773050 | ||||||
chr16:27773054
|
GA | G | 8 | a0001c0001t0004g0049a0001c0004t0002g0070a0001c0004t0002g0073others(5): Show | 8 | HG01243.hp2 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.4199-34delA | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr16 | 27773054 | |||||
chr16:27773230
|
G | A | 1 | a0002c0029t0003g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4309+21G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 23/27 | chr16 | 27773230 | ||||||
chr16:27773607
|
G | A | 12 | a0003c0003t0002g0094a0003c0003t0002g0120a0003c0003t0002g0121others(9): Show | 12 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.4309+398G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 23/27 | chr16 | 27773607 | ||||||
chr16:27773669
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.4309+460T>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 23/27 | chr16 | 27773669 | ||||||
chr16:27774042
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4309+833C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 23/27 | chr16 | 27774042 | ||||||
chr16:27774215
|
C | T | 2 | a0007c0010t0002g0112a0007c0010t0002g0113 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4310-730C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 23/27 | chr16 | 27774215 | ||||||
chr16:27774398
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4310-547A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 23/27 | chr16 | 27774398 | ||||||
chr16:27774559
|
A | G | 4 | a0001c0004t0001g0116a0001c0004t0001g0117a0001c0004t0001g0118others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4310-386A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 23/27 | chr16 | 27774559 | ||||||
chr16:27774824
|
G | A | 21 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(18): Show | 21 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.4310-121G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 23/27 | chr16 | 27774824 | ||||||
chr16:27774869
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4310-76C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 23/27 | chr16 | 27774869 | ||||||
chr16:27774871
|
C | T | 1 | a0004c0007t0010g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4310-74C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 23/27 | chr16 | 27774871 | ||||||
chr16:27774901
|
C | T | 1 | a0002c0002t0003g0072 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4310-44C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 23/27 | chr16 | 27774901 | ||||||
chr16:27775292
|
T | G | 62 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(59): Show |
intron_variant | MODIFIER | c.4449+208T>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/27 | chr16 | 27775292 | ||||||
chr16:27775347
|
C | T | 21 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0027others(18): Show | 21 | HG00099.hp1 HG00140.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.4449+263C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/27 | chr16 | 27775347 | ||||||
chr16:27775458
|
G | A | 1 | a0014c0019t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4449+374G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/27 | chr16 | 27775458 | ||||||
chr16:27775533
|
G | C | 21 | a0001c0004t0001g0042a0002c0002t0003g0062a0002c0002t0003g0063others(18): Show | 21 | HG00099.hp2 HG00408.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.4449+449G>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/27 | chr16 | 27775533 | ||||||
chr16:27775593
|
C | G | 1 | a0001c0001t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.4449+509C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/27 | chr16 | 27775593 | ||||||
chr16:27775679
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4449+595G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/27 | chr16 | 27775679 | ||||||
chr16:27775703
|
CT | C | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.4449+620delT | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/27 | chr16 | 27775703 | ||||||
chr16:27776235
|
C | G | 1 | a0002c0002t0003g0065 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4450-693C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/27 | chr16 | 27776235 | ||||||
chr16:27776257
|
C | T | 2 | a0001c0012t0002g0137a0001c0012t0002g0143 | 2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.4450-671C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/27 | chr16 | 27776257 | ||||||
chr16:27776258
|
C | T | 3 | a0001c0004t0002g0069a0001c0004t0002g0070a0001c0004t0002g0073 | 3 | HG02647.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.4450-670C>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/27 | chr16 | 27776258 | ||||||
chr16:27776446
|
G | A | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.4450-482G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/27 | chr16 | 27776446 | ||||||
chr16:27776599
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.4450-329A>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/27 | chr16 | 27776599 | ||||||
chr16:27776627
|
G | A | 6 | a0001c0005t0002g0147a0001c0005t0002g0148a0001c0005t0002g0149others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.4450-301G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/27 | chr16 | 27776627 | ||||||
chr16:27776680
|
T | C | 29 | a0001c0004t0001g0042a0001c0004t0001g0132a0001c0018t0011g0122others(26): Show | 29 | HG00099.hp2 HG00408.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.4450-248T>C | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/27 | chr16 | 27776680 | ||||||
chr16:27776683
|
G | A | 1 | a0015c0020t0004g0008 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.4450-245G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/27 | chr16 | 27776683 | ||||||
chr16:27776777
|
G | A | 1 | a0004c0030t0005g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4450-151G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 24/27 | chr16 | 27776777 | ||||||
chr16:27777512
|
G | A | 2 | a0001c0012t0002g0137a0001c0012t0002g0143 | 2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.4552-98G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 25/27 | chr16 | 27777512 | ||||||
chr16:27777522
|
C | G | 6 | a0001c0005t0002g0147a0001c0005t0002g0148a0001c0005t0002g0149others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.4552-88C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 25/27 | chr16 | 27777522 | ||||||
chr16:27777526
|
GGCTCAGA others(8): Show |
G | 4 | a0004c0030t0005g0115a0004c0034t0005g0119a0011c0017t0005g0150others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.4552-81_4552-67del others(15): Show |
KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr16 | 27777526 | |||||
chr16:27778209
|
G | A | 3 | a0007c0010t0002g0112a0007c0010t0002g0113a0007c0010t0002g0114 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4801+240G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 27/27 | chr16 | 27778209 | ||||||
chr16:27778288
|
A | T | 3 | a0001c0011t0002g0141a0001c0011t0002g0152a0012c0033t0002g0142 | 3 | HG01243.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.4802-286A>T | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 27/27 | chr16 | 27778288 | ||||||
chr16:27778389
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4802-185G>A | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 27/27 | chr16 | 27778389 | ||||||
chr16:27778552
|
C | G | 1 | a0004c0007t0010g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4802-22C>G | KATNIP | ENSG00000047578.14 | transcript | ENST00000261588.10 | protein_coding | 27/27 | chr16 | 27778552 |