geneid | 54916 |
---|---|
ensemblid | ENSG00000070269.14 |
hgncid | 20185 |
symbol | TMEM260 |
name | transmembrane protein 260 |
refseq_nuc | NM_017799.4 |
refseq_prot | NP_060269.3 |
ensembl_nuc | ENST00000261556.11 |
ensembl_prot | ENSP00000261556.6 |
mane_status | MANE Select |
chr | chr14 |
start | 56579798 |
end | 56649515 |
strand | + |
ver | v1.2 |
region | chr14:56579798-56649515 |
region5000 | chr14:56574798-56654515 |
regionname0 | TMEM260_chr14_56579798_56649515 |
regionname5000 | TMEM260_chr14_56574798_56654515 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 707 | 233 | 60 | 33 | 108 | 8 | 24 | 88 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0002 | 1/1 | 707 | 88 | 14 | 15 | 47 | 1 | 9 | 35 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0003 | 0/0 | 707 | 24 | 6 | 8 | 1 | 3 | 6 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0004 | 0/0 | 707 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0005 | 0/0 | 707 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0006 | 0/0 | 707 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0007 | 0/0 | 707 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0008 | 0/0 | 707 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0009 | 0/0 | 707 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0010 | 0/0 | 707 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0011 | 0/0 | 707 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0012 | 0/0 | 707 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0013 | 0/0 | 707 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0014 | 0/0 | 707 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0015 | 0/0 | 707 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2124 | 124 | 36 | 12 | 57 | 5 | 14 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0002 | 0/0 | 2124 | 75 | 4 | 17 | 44 | 2 | 8 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0003 | 0/0 | 2124 | 34 | 1 | 7 | 26 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0004 | 0/0 | 2124 | 32 | 19 | 3 | 7 | 1 | 2 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0005 | 1/1 | 2124 | 29 | 12 | 5 | 0 | 1 | 9 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0006 | 0/0 | 2124 | 25 | 1 | 3 | 21 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0007 | 0/0 | 2124 | 24 | 6 | 8 | 1 | 3 | 6 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0008 | 0/0 | 2124 | 7 | 5 | 2 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0009 | 0/0 | 2124 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0010 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0011 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0012 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0013 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0014 | 0/0 | 2124 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0015 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0016 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0017 | 0/0 | 2124 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0018 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0019 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0020 | 0/0 | 2124 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
c0021 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2136 | 182 | 40 | 33 | 86 | 5 | 17 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0002 | 0/1 | 2138 | 55 | 8 | 13 | 17 | 5 | 11 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0003 | 0/0 | 2135 | 33 | 0 | 3 | 28 | 1 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0004 | 0/0 | 2135 | 19 | 16 | 3 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0005 | 0/0 | 2136 | 12 | 0 | 3 | 7 | 1 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0006 | 0/0 | 2136 | 12 | 12 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0007 | 0/0 | 2136 | 8 | 0 | 4 | 4 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0008 | 0/0 | 2136 | 7 | 0 | 0 | 7 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0009 | 0/0 | 2137 | 6 | 6 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0010 | 0/0 | 2138 | 5 | 0 | 0 | 5 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0011 | 0/0 | 2134 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0012 | 0/0 | 2137 | 4 | 1 | 0 | 0 | 0 | 3 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0013 | 0/0 | 2135 | 4 | 0 | 0 | 1 | 0 | 3 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0014 | 0/0 | 2135 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0015 | 0/0 | 2135 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0016 | 0/0 | 2135 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0017 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0018 | 0/0 | 2135 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0019 | 0/0 | 2137 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0020 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0021 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0022 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0023 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0024 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
t0025 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0002 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0013 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0015 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0319 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2124 | 124 | 36 | 12 | 57 | 5 | 14 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0002 | 0/0 | 2124 | 75 | 4 | 17 | 44 | 2 | 8 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0004 | 0/0 | 2124 | 32 | 19 | 3 | 7 | 1 | 2 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0011 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0020 | 0/0 | 2124 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0002c0003 | 0/0 | 2124 | 34 | 1 | 7 | 26 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0002c0005 | 1/1 | 2124 | 29 | 12 | 5 | 0 | 1 | 9 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0002c0006 | 0/0 | 2124 | 25 | 1 | 3 | 21 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0003c0007 | 0/0 | 2124 | 24 | 6 | 8 | 1 | 3 | 6 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0004c0008 | 0/0 | 2124 | 7 | 5 | 2 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0005c0009 | 0/0 | 2124 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0006c0019 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0007c0012 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0008c0018 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0009c0017 | 0/0 | 2124 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0010c0016 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0011c0015 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0012c0014 | 0/0 | 2124 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0013c0013 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0014c0010 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0015c0021 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4259 | 42 | 13 | 2 | 21 | 0 | 6 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0001t0002 | 0/0 | 4261 | 43 | 7 | 9 | 16 | 4 | 7 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0001t0005 | 0/0 | 4259 | 10 | 0 | 1 | 7 | 1 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0001t0006 | 0/0 | 4259 | 10 | 10 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0001t0008 | 0/0 | 4259 | 7 | 0 | 0 | 7 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0001t0009 | 0/0 | 4260 | 6 | 6 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0001t0010 | 0/0 | 4261 | 5 | 0 | 0 | 5 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0001t0025 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0002t0001 | 0/0 | 4259 | 73 | 4 | 17 | 43 | 2 | 7 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0002t0019 | 0/0 | 4260 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0002t0023 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0004t0003 | 0/0 | 4258 | 9 | 0 | 0 | 7 | 1 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0004t0004 | 0/0 | 4258 | 16 | 13 | 3 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0004t0011 | 0/0 | 4257 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0004t0014 | 0/0 | 4258 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0004t0015 | 0/0 | 4258 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0004t0016 | 0/0 | 4258 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0011t0001 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0001c0020t0011 | 0/0 | 4257 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0002c0003t0001 | 0/0 | 4259 | 24 | 1 | 4 | 19 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0002c0003t0007 | 0/0 | 4259 | 7 | 0 | 3 | 4 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0002c0003t0017 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0002c0003t0020 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0002c0003t0021 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0002c0005t0001 | 1/0 | 4259 | 13 | 10 | 1 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0002c0005t0002 | 0/1 | 4261 | 11 | 1 | 4 | 0 | 1 | 4 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0002c0005t0012 | 0/0 | 4260 | 4 | 1 | 0 | 0 | 0 | 3 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0002c0005t0013 | 0/0 | 4258 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0002c0006t0001 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0002c0006t0003 | 0/0 | 4258 | 24 | 0 | 3 | 21 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0003c0007t0001 | 0/0 | 4259 | 19 | 5 | 8 | 0 | 3 | 3 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0003c0007t0006 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0003c0007t0013 | 0/0 | 4258 | 3 | 0 | 0 | 1 | 0 | 2 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0003c0007t0022 | 0/0 | 4259 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0004c0008t0004 | 0/0 | 4258 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0004c0008t0005 | 0/0 | 4259 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0004c0008t0006 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0004c0008t0018 | 0/0 | 4258 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0005c0009t0001 | 0/0 | 4259 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0006c0019t0001 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0007c0012t0001 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0008c0018t0001 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0009c0017t0007 | 0/0 | 4259 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0010c0016t0001 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0011c0015t0001 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0012c0014t0024 | 0/0 | 4259 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0013c0013t0001 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0014c0010t0001 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
a0015c0021t0002 | 0/0 | 4261 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | copy fasta | chr14 | 56574798 | 56654515 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0005g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0005g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0005g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0005g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0005g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0008g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0008g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0008g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0008g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0008g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0008g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0008g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0009g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0009g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0009g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0009g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0009g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0009g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0010g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0010g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0001t0025g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0002 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0019g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0002t0023g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0004g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0011g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0011g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0011g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0014g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0015g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0004t0016g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0011t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0001c0020t0011g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0007g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0007g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0007g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0007g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0007g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0007g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0017g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0020g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0003t0021g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0001g0015 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0002g0013 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0002g0319 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0012g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0012g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0012g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0005t0013g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0002c0006t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0006g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0013g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0013g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0013g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0003c0007t0022g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0004c0008t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0004c0008t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0004c0008t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0004c0008t0005g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0004c0008t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0004c0008t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0004c0008t0018g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0005c0009t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0005c0009t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0006c0019t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0007c0012t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0008c0018t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0009c0017t0007g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0010c0016t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0011c0015t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0012c0014t0024g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0013c0013t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0014c0010t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
a0015c0021t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | GBR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00099 | hp2 | a0002 | c0005 | t0002 | g0013 | EUR | GBR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00140 | hp1 | a0003 | c0007 | t0001 | g0270 | EUR | GBR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0203 | EUR | GBR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00280 | hp1 | a0003 | c0007 | t0001 | g0265 | EUR | FIN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0217 | EUR | FIN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0022 | EUR | FIN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0201 | EUR | FIN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00423 | hp2 | a0002 | c0003 | t0001 | g0059 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00438 | hp1 | a0001 | c0002 | t0023 | g0094 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00609 | hp2 | a0002 | c0006 | t0003 | g0308 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00621 | hp1 | a0001 | c0001 | t0005 | g0330 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00621 | hp2 | a0014 | c0010 | t0001 | g0087 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00642 | hp1 | a0002 | c0005 | t0002 | g0014 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00673 | hp2 | a0002 | c0003 | t0001 | g0060 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00735 | hp1 | a0003 | c0007 | t0001 | g0254 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0075 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00738 | hp2 | a0002 | c0005 | t0002 | g0014 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01070 | hp1 | a0002 | c0006 | t0003 | g0288 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01070 | hp2 | a0002 | c0003 | t0001 | g0084 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01071 | hp1 | a0002 | c0006 | t0003 | g0289 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01081 | hp2 | a0001 | c0004 | t0004 | g0190 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01099 | hp2 | a0009 | c0017 | t0007 | g0019 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01109 | hp1 | a0005 | c0009 | t0001 | g0169 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01109 | hp2 | a0003 | c0007 | t0001 | g0255 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01167 | hp2 | a0003 | c0007 | t0001 | g0256 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01175 | hp2 | a0003 | c0007 | t0001 | g0250 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01243 | hp1 | a0001 | c0004 | t0004 | g0187 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01243 | hp2 | a0001 | c0004 | t0004 | g0182 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01255 | hp2 | a0003 | c0007 | t0001 | g0261 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01256 | hp1 | a0002 | c0003 | t0001 | g0050 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01256 | hp2 | a0003 | c0007 | t0001 | g0253 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01261 | hp1 | a0003 | c0007 | t0001 | g0249 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0334 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0066 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01361 | hp2 | a0002 | c0005 | t0002 | g0219 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01433 | hp1 | a0001 | c0020 | t0011 | g0313 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01433 | hp2 | a0004 | c0008 | t0005 | g0251 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01496 | hp1 | a0002 | c0003 | t0007 | g0112 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01884 | hp1 | a0003 | c0007 | t0006 | g0267 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01884 | hp2 | a0002 | c0005 | t0001 | g0011 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0197 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01891 | hp2 | a0002 | c0005 | t0001 | g0012 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01934 | hp2 | a0002 | c0005 | t0002 | g0230 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01943 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01943 | hp2 | a0004 | c0008 | t0005 | g0268 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01978 | hp1 | a0003 | c0007 | t0001 | g0263 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01978 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01981 | hp2 | a0002 | c0005 | t0001 | g0015 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0052 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02015 | hp1 | a0002 | c0006 | t0003 | g0283 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02027 | hp1 | a0002 | c0003 | t0001 | g0099 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02040 | hp2 | a0001 | c0001 | t0008 | g0322 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02055 | hp1 | a0002 | c0005 | t0002 | g0013 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02074 | hp1 | a0002 | c0003 | t0020 | g0090 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02074 | hp2 | a0001 | c0001 | t0010 | g0004 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02080 | hp1 | a0002 | c0006 | t0003 | g0317 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02080 | hp2 | a0002 | c0003 | t0007 | g0032 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02132 | hp1 | a0002 | c0003 | t0001 | g0049 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02135 | hp1 | a0002 | c0003 | t0017 | g0318 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02135 | hp2 | a0002 | c0003 | t0001 | g0098 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02145 | hp1 | a0011 | c0015 | t0001 | g0048 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02145 | hp2 | a0001 | c0004 | t0004 | g0181 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02148 | hp1 | a0002 | c0003 | t0007 | g0020 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | CDX | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02257 | hp1 | a0002 | c0005 | t0001 | g0175 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02280 | hp2 | a0001 | c0001 | t0006 | g0244 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02300 | hp2 | a0002 | c0006 | t0003 | g0287 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02451 | hp1 | a0001 | c0001 | t0009 | g0196 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02451 | hp2 | a0003 | c0007 | t0001 | g0271 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02523 | hp1 | a0001 | c0001 | t0008 | g0124 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02572 | hp1 | a0003 | c0007 | t0001 | g0269 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0195 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02622 | hp2 | a0001 | c0004 | t0004 | g0188 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02630 | hp1 | a0001 | c0004 | t0004 | g0189 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0246 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02698 | hp1 | a0003 | c0007 | t0001 | g0258 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02698 | hp2 | a0002 | c0005 | t0002 | g0150 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02717 | hp1 | a0003 | c0007 | t0001 | g0273 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02717 | hp2 | a0007 | c0012 | t0001 | g0120 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02738 | hp1 | a0001 | c0004 | t0016 | g0304 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02738 | hp2 | a0001 | c0001 | t0005 | g0324 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02809 | hp1 | a0004 | c0008 | t0006 | g0114 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02809 | hp2 | a0001 | c0001 | t0006 | g0118 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02818 | hp1 | a0001 | c0004 | t0004 | g0191 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0117 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02886 | hp2 | a0001 | c0004 | t0004 | g0186 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02895 | hp1 | a0002 | c0005 | t0001 | g0233 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0116 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0113 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02922 | hp2 | a0001 | c0004 | t0014 | g0017 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02965 | hp2 | a0001 | c0004 | t0004 | g0005 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0245 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02970 | hp2 | a0002 | c0005 | t0012 | g0174 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02976 | hp1 | a0002 | c0005 | t0001 | g0011 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03017 | hp1 | a0002 | c0005 | t0012 | g0133 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0037 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03041 | hp1 | a0001 | c0004 | t0014 | g0017 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03041 | hp2 | a0003 | c0007 | t0001 | g0272 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03130 | hp1 | a0001 | c0004 | t0004 | g0005 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03130 | hp2 | a0013 | c0013 | t0001 | g0171 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03139 | hp2 | a0003 | c0007 | t0001 | g0252 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03195 | hp1 | a0001 | c0004 | t0004 | g0184 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03195 | hp2 | a0004 | c0008 | t0004 | g0129 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03209 | hp1 | a0001 | c0004 | t0004 | g0185 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03209 | hp2 | a0005 | c0009 | t0001 | g0164 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03225 | hp1 | a0001 | c0001 | t0009 | g0199 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03225 | hp2 | a0002 | c0005 | t0001 | g0275 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03239 | hp1 | a0001 | c0004 | t0003 | g0298 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03239 | hp2 | a0002 | c0005 | t0002 | g0151 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03453 | hp1 | a0004 | c0008 | t0004 | g0128 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03486 | hp1 | a0001 | c0011 | t0001 | g0320 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03486 | hp2 | a0004 | c0008 | t0004 | g0178 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0080 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03516 | hp2 | a0002 | c0005 | t0001 | g0170 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0078 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03579 | hp1 | a0010 | c0016 | t0001 | g0092 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03579 | hp2 | a0002 | c0005 | t0001 | g0176 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03669 | hp1 | a0002 | c0005 | t0002 | g0214 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0177 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03688 | hp1 | a0002 | c0005 | t0001 | g0168 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03688 | hp2 | a0002 | c0005 | t0002 | g0160 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03704 | hp2 | a0012 | c0014 | t0024 | g0035 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03710 | hp1 | a0002 | c0005 | t0012 | g0131 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0100 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03831 | hp2 | a0003 | c0007 | t0013 | g0262 | SAS | BEB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03834 | hp2 | a0003 | c0007 | t0001 | g0016 | SAS | BEB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | BEB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG03927 | hp2 | a0003 | c0007 | t0001 | g0016 | SAS | BEB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0243 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0107 | SAS | BEB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG04184 | hp2 | a0003 | c0007 | t0013 | g0259 | SAS | BEB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG04199 | hp1 | a0001 | c0002 | t0019 | g0029 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG04199 | hp2 | a0002 | c0005 | t0013 | g0211 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0105 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG04228 | hp1 | a0003 | c0007 | t0022 | g0260 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0115 | AFR | YRI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18522 | hp2 | a0001 | c0001 | t0009 | g0198 | AFR | YRI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18612 | hp2 | a0002 | c0006 | t0003 | g0279 | EAS | CHB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | CHB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18747 | hp2 | a0006 | c0019 | t0001 | g0045 | EAS | CHB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | YRI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18906 | hp2 | a0001 | c0004 | t0004 | g0180 | AFR | YRI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18939 | hp1 | a0001 | c0004 | t0003 | g0297 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18942 | hp2 | a0001 | c0001 | t0010 | g0004 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18943 | hp2 | a0001 | c0001 | t0008 | g0127 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18945 | hp2 | a0001 | c0001 | t0005 | g0332 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18951 | hp2 | a0002 | c0003 | t0007 | g0040 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18952 | hp1 | a0002 | c0003 | t0001 | g0093 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18953 | hp1 | a0002 | c0003 | t0001 | g0038 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18956 | hp1 | a0002 | c0003 | t0001 | g0030 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18959 | hp1 | a0001 | c0001 | t0005 | g0325 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18963 | hp1 | a0002 | c0003 | t0001 | g0057 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18963 | hp2 | a0001 | c0004 | t0003 | g0306 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18964 | hp1 | a0001 | c0004 | t0003 | g0296 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18965 | hp2 | a0002 | c0006 | t0003 | g0286 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18967 | hp1 | a0001 | c0001 | t0025 | g0328 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18970 | hp1 | a0001 | c0001 | t0005 | g0329 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18970 | hp2 | a0002 | c0003 | t0001 | g0031 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18978 | hp1 | a0001 | c0001 | t0008 | g0125 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18979 | hp1 | a0002 | c0003 | t0001 | g0064 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18979 | hp2 | a0002 | c0006 | t0003 | g0302 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18980 | hp1 | a0002 | c0003 | t0001 | g0082 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18980 | hp2 | a0002 | c0006 | t0003 | g0293 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18982 | hp1 | a0001 | c0001 | t0010 | g0004 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0331 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18983 | hp2 | a0002 | c0003 | t0001 | g0192 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18984 | hp1 | a0001 | c0004 | t0003 | g0281 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18989 | hp1 | a0001 | c0001 | t0008 | g0321 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18989 | hp2 | a0002 | c0006 | t0003 | g0309 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18993 | hp1 | a0002 | c0003 | t0001 | g0081 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18993 | hp2 | a0001 | c0004 | t0003 | g0295 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18998 | hp2 | a0001 | c0004 | t0003 | g0305 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18999 | hp1 | a0008 | c0018 | t0001 | g0003 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19000 | hp1 | a0002 | c0006 | t0003 | g0282 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19000 | hp2 | a0002 | c0003 | t0007 | g0003 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19002 | hp1 | a0002 | c0006 | t0003 | g0284 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19003 | hp1 | a0002 | c0006 | t0003 | g0290 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19005 | hp2 | a0002 | c0006 | t0003 | g0300 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19007 | hp1 | a0002 | c0006 | t0003 | g0299 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19009 | hp1 | a0001 | c0001 | t0008 | g0323 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19010 | hp2 | a0002 | c0003 | t0001 | g0110 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19030 | hp1 | a0001 | c0004 | t0011 | g0311 | AFR | LWK | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19030 | hp2 | a0001 | c0004 | t0004 | g0179 | AFR | LWK | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19043 | hp1 | a0002 | c0005 | t0001 | g0172 | AFR | LWK | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19043 | hp2 | a0001 | c0004 | t0015 | g0314 | AFR | LWK | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19056 | hp2 | a0002 | c0006 | t0003 | g0285 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19058 | hp1 | a0002 | c0006 | t0003 | g0294 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19064 | hp1 | a0003 | c0007 | t0013 | g0266 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19065 | hp1 | a0002 | c0006 | t0003 | g0303 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19066 | hp1 | a0002 | c0003 | t0001 | g0061 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19070 | hp2 | a0001 | c0001 | t0010 | g0004 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19074 | hp2 | a0002 | c0003 | t0001 | g0193 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19077 | hp1 | a0002 | c0006 | t0003 | g0316 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19078 | hp1 | a0002 | c0003 | t0007 | g0036 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19078 | hp2 | a0001 | c0001 | t0005 | g0326 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19079 | hp1 | a0002 | c0003 | t0021 | g0042 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19080 | hp2 | a0002 | c0003 | t0001 | g0071 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19081 | hp1 | a0001 | c0001 | t0008 | g0126 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19082 | hp1 | a0002 | c0006 | t0003 | g0280 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19083 | hp1 | a0001 | c0001 | t0005 | g0327 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19085 | hp1 | a0002 | c0006 | t0003 | g0315 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19086 | hp1 | a0001 | c0001 | t0010 | g0239 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19086 | hp2 | a0002 | c0006 | t0003 | g0291 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19087 | hp1 | a0001 | c0004 | t0003 | g0301 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19087 | hp2 | a0015 | c0021 | t0002 | g0006 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19089 | hp1 | a0002 | c0003 | t0001 | g0101 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19091 | hp1 | a0002 | c0006 | t0003 | g0292 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19240 | hp1 | a0004 | c0008 | t0018 | g0119 | AFR | YRI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | ASW | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA20129 | hp2 | a0001 | c0004 | t0011 | g0310 | AFR | ASW | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA20752 | hp1 | a0001 | c0004 | t0003 | g0307 | EUR | TSI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA20752 | hp2 | a0001 | c0001 | t0005 | g0333 | EUR | TSI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0207 | EUR | TSI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA20805 | hp2 | a0003 | c0007 | t0001 | g0257 | EUR | TSI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA20905 | hp1 | a0002 | c0005 | t0012 | g0132 | SAS | GIH | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | GIH | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG01123 | hp2 | a0002 | c0003 | t0007 | g0018 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0247 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02109 | hp2 | a0001 | c0004 | t0004 | g0183 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02486 | hp1 | a0001 | c0004 | t0004 | g0005 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02486 | hp2 | a0001 | c0001 | t0006 | g0248 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG02559 | hp2 | a0001 | c0004 | t0011 | g0312 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG06807 | hp1 | a0001 | c0001 | t0009 | g0194 | AFR | USA | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
HG06807 | hp2 | a0002 | c0005 | t0001 | g0012 | AFR | USA | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | USA | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA20300 | hp2 | a0002 | c0003 | t0001 | g0085 | AFR | USA | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | LWK | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
NA21309 | hp2 | a0002 | c0006 | t0001 | g0264 | AFR | LWK | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
homoSapiens_chm13v2 | hp1 | a0002 | c0005 | t0002 | g0319 | REF | REF | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
homoSapiens_grch38 | hp1 | a0002 | c0005 | t0001 | g0015 | REF | REF | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:56580018
|
C | T | 1 | a0015 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.104C>T | p.Ala35Val | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/16 | 221/4259 | 104/2124 | 35/707 | chr14 | 56580018 | ||
chr14:56580050
|
C | A | 1 | a0014 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.136C>A | p.Pro46Thr | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/16 | 253/4259 | 136/2124 | 46/707 | chr14 | 56580050 | ||
chr14:56585852
|
A | G | 1 | a0013 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.284A>G | p.Asn95Ser | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/16 | 401/4259 | 284/2124 | 95/707 | chr14 | 56585852 | ||
chr14:56609137
|
G | T | 1 | a0005 | 2 | HG01109.hp1 HG03209.hp2 |
missense_variant | MODERATE | c.668G>T | p.Ser223Ile | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/16 | 785/4259 | 668/2124 | 223/707 | chr14 | 56609137 | ||
chr14:56609202
|
G | T | 2 | a0003a0004 | 31 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(28): Show |
missense_variant | MODERATE | c.733G>T | p.Ala245Ser | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/16 | 850/4259 | 733/2124 | 245/707 | chr14 | 56609202 | ||
chr14:56616015
|
G | A | 1 | a0012 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.929G>A | p.Cys310Tyr | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/16 | 1046/4259 | 929/2124 | 310/707 | chr14 | 56616015 | ||
chr14:56625394
|
G | A | 1 | a0011 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.1411G>A | p.Glu471Lys | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/16 | 1528/4259 | 1411/2124 | 471/707 | chr14 | 56625394 | ||
chr14:56632995
|
A | C | 1 | a0006 | 1 | NA18747.hp2 | missense_variant&splice_region_variant | MODERATE | c.1548A>C | p.Gln516His | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/16 | 1665/4259 | 1548/2124 | 516/707 | chr14 | 56632995 | ||
chr14:56633102
|
T | C | 1 | a0010 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.1655T>C | p.Ile552Thr | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/16 | 1772/4259 | 1655/2124 | 552/707 | chr14 | 56633102 | ||
chr14:56633141
|
G | A | 9 | a0001a0004a0005others(6): Show | 248 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(245): Show |
missense_variant | MODERATE | c.1694G>A | p.Ser565Asn | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/16 | 1811/4259 | 1694/2124 | 565/707 | chr14 | 56633141 | ||
chr14:56634924
|
G | T | 1 | a0008 | 1 | NA18999.hp1 | missense_variant | MODERATE | c.1750G>T | p.Val584Leu | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/16 | 1867/4259 | 1750/2124 | 584/707 | chr14 | 56634924 | ||
chr14:56636584
|
G | A | 1 | a0007 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1855G>A | p.Ala619Thr | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/16 | 1972/4259 | 1855/2124 | 619/707 | chr14 | 56636584 | ||
chr14:56647339
|
A | G | 1 | a0009 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.1966A>G | p.Arg656Gly | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 2083/4259 | 1966/2124 | 656/707 | chr14 | 56647339 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:56580070
|
C | T | 1 | a0001c0020 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.156C>T | p.Asp52Asp | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/16 | 273/4259 | 156/2124 | 52/707 | chr14 | 56580070 | ||
chr14:56585793
|
G | T | 9 | a0001c0002a0002c0003a0006c0019others(6): Show | 116 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
synonymous_variant | LOW | c.225G>T | p.Thr75Thr | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/16 | 342/4259 | 225/2124 | 75/707 | chr14 | 56585793 | ||
chr14:56585829
|
T | C | 1 | a0001c0011 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.261T>C | p.Phe87Phe | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/16 | 378/4259 | 261/2124 | 87/707 | chr14 | 56585829 | ||
chr14:56605620
|
C | T | 3 | a0001c0004a0001c0020a0002c0006 | 58 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(55): Show |
synonymous_variant | LOW | c.573C>T | p.His191His | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/16 | 690/4259 | 573/2124 | 191/707 | chr14 | 56605620 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:56579798
|
G | T | 1 | a0001c0001t0025 | 1 | NA18967.hp1 | 5_prime_UTR_variant | MODIFIER | c.-117G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/16 | 117 | chr14 | 56579798 | |||||
chr14:56579846
|
C | G | 1 | a0001c0001t0010 | 5 | HG02074.hp2 NA18942.hp2 NA18982.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-69C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/16 | 69 | chr14 | 56579846 | |||||
chr14:56579888
|
T | A | 8 | a0001c0004t0003a0001c0004t0011a0001c0004t0014others(5): Show | 42 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
5_prime_UTR_variant | MODIFIER | c.-27T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/16 | 27 | chr14 | 56579888 | |||||
chr14:56647567
|
C | CA | 5 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(2): Show | 66 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*72dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 73 | INFO_REALIGN_3_PRIME | chr14 | 56647567 | ||||
chr14:56647604
|
C | T | 1 | a0012c0014t0024 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*107C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 107 | chr14 | 56647604 | |||||
chr14:56647667
|
G | A | 11 | a0001c0001t0005a0001c0001t0008a0001c0001t0025others(8): Show | 81 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*170G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 170 | chr14 | 56647667 | |||||
chr14:56647816
|
C | G | 3 | a0001c0001t0006a0003c0007t0006a0004c0008t0006 | 12 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*319C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 319 | chr14 | 56647816 | |||||
chr14:56647854
|
T | C | 5 | a0001c0004t0011a0001c0004t0014a0001c0004t0015others(2): Show | 8 | HG01433.hp1 HG02559.hp2 HG02738.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*357T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 357 | chr14 | 56647854 | |||||
chr14:56647922
|
G | GA | 5 | a0001c0001t0002a0001c0001t0010a0001c0002t0019others(2): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*435dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 436 | INFO_REALIGN_3_PRIME | chr14 | 56647922 | ||||
chr14:56647922
|
GA | G | 15 | a0001c0001t0005a0001c0001t0008a0001c0001t0025others(12): Show | 84 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*435delA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 435 | INFO_REALIGN_3_PRIME | chr14 | 56647922 | ||||
chr14:56648029
|
T | A | 1 | a0004c0008t0018 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*532T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 532 | chr14 | 56648029 | |||||
chr14:56648268
|
T | TG | 4 | a0001c0001t0005a0001c0001t0008a0001c0001t0025others(1): Show | 20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*778dupG | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 779 | INFO_REALIGN_3_PRIME | chr14 | 56648268 | ||||
chr14:56648482
|
C | G | 1 | a0001c0004t0016 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*985C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 985 | chr14 | 56648482 | |||||
chr14:56648688
|
G | C | 1 | a0002c0003t0020 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1191G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 1191 | chr14 | 56648688 | |||||
chr14:56648904
|
C | G | 5 | a0001c0002t0023a0001c0004t0003a0002c0005t0013others(2): Show | 38 | HG00438.hp1 HG00609.hp2 HG01070.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1407C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 1407 | chr14 | 56648904 | |||||
chr14:56648935
|
T | G | 1 | a0002c0003t0021 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1438T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 1438 | chr14 | 56648935 | |||||
chr14:56648962
|
G | T | 1 | a0003c0007t0022 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1465G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 1465 | chr14 | 56648962 | |||||
chr14:56649373
|
T | TG | 1 | a0002c0005t0012 | 4 | HG02970.hp2 HG03017.hp1 HG03710.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1878dupG | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 1879 | INFO_REALIGN_3_PRIME | chr14 | 56649373 | ||||
chr14:56649421
|
T | C | 3 | a0001c0001t0005a0001c0001t0025a0004c0008t0005 | 13 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1924T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 1924 | chr14 | 56649421 | |||||
chr14:56649474
|
TA | T | 3 | a0001c0004t0011a0001c0004t0015a0001c0020t0011 | 5 | HG01433.hp1 HG02559.hp2 NA19030.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1987delA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 1987 | INFO_REALIGN_3_PRIME | chr14 | 56649474 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:56580111
|
C | A | 101 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(98): Show | 112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.160+37C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580111 | ||||||
chr14:56580148
|
C | T | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.160+74C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580148 | ||||||
chr14:56580195
|
C | G | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.160+121C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580195 | ||||||
chr14:56580311
|
G | A | 7 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(4): Show | 7 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+237G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580311 | ||||||
chr14:56580425
|
A | G | 1 | a0001c0011t0001g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+351A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580425 | ||||||
chr14:56580497
|
A | G | 1 | a0002c0005t0002g0319 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.160+423A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580497 | ||||||
chr14:56580532
|
A | G | 1 | a0002c0003t0007g0112 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.160+458A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580532 | ||||||
chr14:56580546
|
A | G | 1 | a0001c0011t0001g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+472A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580546 | ||||||
chr14:56580562
|
G | C | 2 | a0001c0001t0001g0121a0007c0012t0001g0120 | 2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.160+488G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580562 | ||||||
chr14:56580632
|
C | G | 42 | a0001c0001t0002g0278a0001c0004t0003g0281a0001c0004t0003g0295others(39): Show | 43 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.160+558C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580632 | ||||||
chr14:56580755
|
C | T | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160+681C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580755 | ||||||
chr14:56580764
|
T | C | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160+690T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580764 | ||||||
chr14:56580822
|
T | C | 2 | a0001c0001t0002g0122a0001c0001t0002g0123 | 2 | NA18945.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.160+748T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580822 | ||||||
chr14:56580928
|
C | T | 1 | a0002c0005t0001g0275 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.160+854C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580928 | ||||||
chr14:56580937
|
C | T | 1 | a0001c0001t0002g0274 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.160+863C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580937 | ||||||
chr14:56581024
|
A | G | 1 | a0001c0011t0001g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+950A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581024 | ||||||
chr14:56581213
|
A | G | 1 | a0001c0011t0001g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+1139A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581213 | ||||||
chr14:56581326
|
G | A | 298 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(295): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.160+1252G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581326 | ||||||
chr14:56581489
|
G | C | 1 | a0001c0001t0006g0113 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+1415G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581489 | ||||||
chr14:56581802
|
C | T | 1 | a0001c0002t0001g0111 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.160+1728C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581802 | ||||||
chr14:56581811
|
C | T | 59 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0122others(56): Show | 65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.160+1737C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581811 | ||||||
chr14:56581817
|
T | G | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.160+1743T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581817 | ||||||
chr14:56581819
|
A | G | 59 | a0001c0001t0002g0278a0001c0004t0003g0281a0001c0004t0003g0295others(56): Show | 62 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.160+1745A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581819 | ||||||
chr14:56581964
|
G | A | 3 | a0002c0003t0007g0018a0002c0003t0007g0020a0009c0017t0007g0019 | 3 | HG01099.hp2 HG01123.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.160+1890G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581964 | ||||||
chr14:56582093
|
C | T | 1 | a0001c0001t0002g0243 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.160+2019C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56582093 | ||||||
chr14:56582255
|
C | A | 2 | a0001c0001t0002g0278a0001c0004t0014g0017 | 3 | HG02559.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.160+2181C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56582255 | ||||||
chr14:56582279
|
C | G | 125 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0005g0324others(122): Show | 136 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.160+2205C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56582279 | ||||||
chr14:56582396
|
A | G | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.160+2322A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56582396 | ||||||
chr14:56582523
|
C | T | 2 | a0002c0005t0001g0175a0002c0005t0001g0176 | 2 | HG02257.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.160+2449C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56582523 | ||||||
chr14:56582614
|
C | T | 2 | a0001c0002t0001g0109a0002c0003t0001g0110 | 2 | NA19010.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.161-2387C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56582614 | ||||||
chr14:56582777
|
C | G | 53 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0122others(50): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.161-2224C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56582777 | ||||||
chr14:56582935
|
TTTATC | T | 102 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(99): Show | 113 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.161-2063_161-2059d others(7): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 56582935 | |||||
chr14:56582947
|
G | A | 3 | a0001c0001t0008g0321a0001c0001t0008g0322a0001c0001t0008g0323 | 3 | HG02040.hp2 NA18989.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.161-2054G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56582947 | ||||||
chr14:56583145
|
A | T | 2 | a0001c0001t0002g0278a0001c0004t0014g0017 | 3 | HG02559.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.161-1856A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56583145 | ||||||
chr14:56583208
|
C | G | 1 | a0001c0002t0001g0177 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.161-1793C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56583208 | ||||||
chr14:56583248
|
T | G | 105 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(102): Show | 116 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.161-1753T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56583248 | ||||||
chr14:56583253
|
G | C | 1 | a0001c0001t0006g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.161-1748G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56583253 | ||||||
chr14:56583490
|
G | A | 6 | a0001c0001t0008g0124a0001c0001t0008g0125a0001c0001t0008g0126others(3): Show | 6 | HG02523.hp1 HG03195.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-1511G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56583490 | ||||||
chr14:56583503
|
A | G | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-1498A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56583503 | ||||||
chr14:56583894
|
A | G | 1 | a0004c0008t0018g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.161-1107A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56583894 | ||||||
chr14:56583903
|
G | A | 4 | a0001c0001t0008g0124a0001c0001t0008g0125a0001c0001t0008g0126others(1): Show | 4 | HG02523.hp1 NA18943.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-1098G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56583903 | ||||||
chr14:56583906
|
C | CGTCA | 44 | a0001c0001t0002g0278a0001c0004t0003g0281a0001c0004t0003g0295others(41): Show | 45 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.161-1094_161-1091d others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 56583906 | |||||
chr14:56583990
|
T | TTG | 18 | a0001c0004t0011g0310a0001c0004t0011g0311a0001c0004t0011g0312others(15): Show | 19 | HG00140.hp1 HG00609.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.161-975_161-974dup others(2): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 56583990 | |||||
chr14:56583990
|
T | TTGTG | 11 | a0001c0001t0005g0325a0001c0001t0005g0326a0001c0001t0005g0327others(8): Show | 11 | HG00621.hp1 HG01358.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.161-977_161-974dup others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 56583990 | |||||
chr14:56583990
|
T | TTGTGTGT others(1): Show |
3 | a0001c0001t0008g0321a0001c0001t0008g0322a0001c0001t0008g0323 | 3 | HG02040.hp2 NA18989.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.161-981_161-974dup others(8): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 56583990 | |||||
chr14:56583990
|
TTG | T | 107 | a0001c0001t0001g0121a0001c0001t0001g0165a0001c0001t0001g0166others(104): Show | 123 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.161-975_161-974del others(2): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 56583990 | |||||
chr14:56583990
|
TTGTG | T | 123 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(120): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.161-977_161-974del others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 56583990 | |||||
chr14:56583990
|
TTGTGTGT others(11): Show |
T | 1 | a0001c0002t0001g0021 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.161-991_161-974del others(18): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 56583990 | |||||
chr14:56584084
|
A | G | 15 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(12): Show | 17 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.161-917A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584084 | ||||||
chr14:56584179
|
G | C | 15 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(12): Show | 17 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.161-822G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584179 | ||||||
chr14:56584382
|
T | C | 1 | a0004c0008t0018g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.161-619T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584382 | ||||||
chr14:56584441
|
G | A | 1 | a0002c0005t0001g0275 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.161-560G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584441 | ||||||
chr14:56584473
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.161-528C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584473 | ||||||
chr14:56584630
|
G | A | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-371G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584630 | ||||||
chr14:56584630
|
G | T | 2 | a0002c0003t0001g0098a0002c0003t0001g0099 | 2 | HG02027.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.161-371G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584630 | ||||||
chr14:56584672
|
A | G | 1 | a0001c0001t0009g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.161-329A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584672 | ||||||
chr14:56584729
|
C | T | 1 | a0003c0007t0001g0265 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.161-272C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584729 | ||||||
chr14:56584773
|
C | G | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-228C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584773 | ||||||
chr14:56584775
|
A | G | 2 | a0001c0002t0001g0096a0001c0002t0001g0097 | 2 | NA19002.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.161-226A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584775 | ||||||
chr14:56584791
|
C | T | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.161-210C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584791 | ||||||
chr14:56584812
|
T | C | 4 | a0001c0001t0005g0325a0001c0001t0005g0326a0001c0001t0005g0327others(1): Show | 4 | NA18959.hp1 NA18967.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-189T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584812 | ||||||
chr14:56584879
|
G | T | 2 | a0001c0001t0001g0121a0007c0012t0001g0120 | 2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.161-122G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584879 | ||||||
chr14:56584971
|
A | G | 1 | a0001c0002t0001g0095 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.161-30A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584971 | ||||||
chr14:56585174
|
ATTTAC | A | 7 | a0001c0004t0004g0179a0001c0004t0004g0180a0001c0004t0004g0181others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+147_192+151del others(5): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 56585174 | |||||
chr14:56585246
|
CTTA | C | 3 | a0002c0006t0003g0280a0002c0006t0003g0308a0003c0007t0001g0265 | 3 | HG00280.hp1 HG00609.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.192+219_192+221del others(3): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 56585246 | |||||
chr14:56585537
|
C | T | 2 | a0001c0001t0002g0238a0002c0005t0002g0014 | 3 | HG00642.hp1 HG00738.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.193-224C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 2/15 | chr14 | 56585537 | ||||||
chr14:56585564
|
G | A | 114 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(111): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.193-197G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 2/15 | chr14 | 56585564 | ||||||
chr14:56586069
|
C | T | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+157C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586069 | ||||||
chr14:56586179
|
G | A | 310 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(307): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.344+267G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586179 | ||||||
chr14:56586204
|
A | T | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+292A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586204 | ||||||
chr14:56586272
|
C | T | 1 | a0001c0002t0023g0094 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.344+360C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586272 | ||||||
chr14:56586297
|
G | A | 1 | a0004c0008t0018g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.344+385G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586297 | ||||||
chr14:56586304
|
C | T | 112 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(109): Show | 123 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.344+392C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586304 | ||||||
chr14:56586305
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.344+393C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586305 | ||||||
chr14:56586377
|
A | G | 1 | a0001c0002t0001g0108 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.344+465A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586377 | ||||||
chr14:56586415
|
G | A | 2 | a0004c0008t0004g0128a0004c0008t0004g0129 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.344+503G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586415 | ||||||
chr14:56586461
|
T | C | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+549T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586461 | ||||||
chr14:56586515
|
A | G | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.344+603A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586515 | ||||||
chr14:56586635
|
G | A | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+723G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586635 | ||||||
chr14:56586675
|
A | T | 8 | a0001c0001t0002g0232a0001c0001t0002g0234a0001c0001t0002g0235others(5): Show | 8 | HG01358.hp1 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+763A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586675 | ||||||
chr14:56586936
|
T | G | 5 | a0001c0001t0006g0244a0001c0001t0006g0245a0001c0001t0006g0246others(2): Show | 5 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+1024T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586936 | ||||||
chr14:56587035
|
G | C | 5 | a0001c0001t0006g0244a0001c0001t0006g0245a0001c0001t0006g0246others(2): Show | 5 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+1123G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56587035 | ||||||
chr14:56587147
|
T | C | 131 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0005g0324others(128): Show | 142 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.344+1235T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56587147 | ||||||
chr14:56587266
|
T | G | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+1354T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56587266 | ||||||
chr14:56587386
|
T | C | 106 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(103): Show | 117 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.344+1474T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56587386 | ||||||
chr14:56587529
|
G | A | 4 | a0001c0001t0006g0245a0001c0001t0006g0246a0001c0001t0006g0247others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+1617G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56587529 | ||||||
chr14:56587741
|
T | C | 5 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0025others(2): Show | 5 | HG00733.hp1 HG00735.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+1829T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56587741 | ||||||
chr14:56587744
|
G | A | 1 | a0003c0007t0013g0266 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.344+1832G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56587744 | ||||||
chr14:56587775
|
T | G | 1 | a0001c0002t0001g0028 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.344+1863T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56587775 | ||||||
chr14:56588103
|
C | T | 53 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0122others(50): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.344+2191C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56588103 | ||||||
chr14:56588566
|
A | G | 1 | a0001c0004t0003g0307 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.344+2654A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56588566 | ||||||
chr14:56588568
|
CT | C | 55 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(52): Show | 60 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.344+2659delT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56588568 | |||||
chr14:56588576
|
A | G | 1 | a0002c0005t0001g0275 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.344+2664A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56588576 | ||||||
chr14:56588710
|
G | GTATT | 310 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(307): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.344+2802_344+2805d others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56588710 | |||||
chr14:56588780
|
A | G | 1 | a0002c0005t0001g0275 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.344+2868A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56588780 | ||||||
chr14:56588918
|
G | A | 1 | a0001c0002t0019g0029 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.344+3006G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56588918 | ||||||
chr14:56589134
|
T | C | 5 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0192others(2): Show | 5 | HG02135.hp1 NA18956.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+3222T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589134 | ||||||
chr14:56589209
|
C | T | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.344+3297C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589209 | ||||||
chr14:56589254
|
C | T | 1 | a0001c0011t0001g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.344+3342C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589254 | ||||||
chr14:56589277
|
C | T | 1 | a0001c0004t0004g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.344+3365C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589277 | ||||||
chr14:56589284
|
G | A | 2 | a0003c0007t0001g0249a0003c0007t0001g0250 | 2 | HG01175.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.344+3372G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589284 | ||||||
chr14:56589315
|
G | A | 6 | a0001c0004t0004g0179a0001c0004t0004g0180a0001c0004t0004g0181others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.344+3403G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589315 | ||||||
chr14:56589316
|
C | G | 7 | a0002c0005t0001g0011a0002c0005t0001g0012a0002c0005t0001g0170others(4): Show | 9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.344+3404C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589316 | ||||||
chr14:56589368
|
C | T | 106 | a0001c0001t0002g0231a0001c0002t0001g0001a0001c0002t0001g0002others(103): Show | 117 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.344+3456C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589368 | ||||||
chr14:56589656
|
C | T | 105 | a0001c0001t0002g0231a0001c0002t0001g0001a0001c0002t0001g0002others(102): Show | 116 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.344+3744C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589656 | ||||||
chr14:56589887
|
A | G | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.344+3975A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589887 | ||||||
chr14:56590072
|
C | T | 59 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(56): Show | 66 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.344+4160C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56590072 | ||||||
chr14:56590109
|
G | A | 1 | a0007c0012t0001g0120 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.344+4197G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56590109 | ||||||
chr14:56590243
|
G | A | 1 | a0001c0004t0004g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.344+4331G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56590243 | ||||||
chr14:56590277
|
A | T | 1 | a0001c0001t0009g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.344+4365A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56590277 | ||||||
chr14:56590312
|
C | T | 1 | a0001c0001t0006g0118 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.344+4400C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56590312 | ||||||
chr14:56590317
|
C | G | 1 | a0002c0005t0002g0230 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.344+4405C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56590317 | ||||||
chr14:56591407
|
C | A | 15 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(12): Show | 17 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.344+5495C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56591407 | ||||||
chr14:56591435
|
G | C | 1 | a0001c0002t0001g0028 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.344+5523G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56591435 | ||||||
chr14:56591527
|
G | A | 15 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(12): Show | 17 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.344+5615G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56591527 | ||||||
chr14:56591628
|
T | G | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.344+5716T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56591628 | ||||||
chr14:56591796
|
T | C | 4 | a0002c0005t0001g0011a0002c0005t0001g0012a0002c0005t0001g0170others(1): Show | 6 | HG01884.hp2 HG01891.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.344+5884T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56591796 | ||||||
chr14:56591829
|
C | T | 41 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(38): Show | 42 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.344+5917C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56591829 | ||||||
chr14:56592230
|
G | A | 56 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(53): Show | 59 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.344+6318G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56592230 | ||||||
chr14:56592356
|
A | T | 1 | a0001c0004t0004g0189 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.344+6444A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56592356 | ||||||
chr14:56592370
|
C | G | 1 | a0002c0006t0003g0317 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.344+6458C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56592370 | ||||||
chr14:56592662
|
T | G | 19 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(16): Show | 19 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.344+6750T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56592662 | ||||||
chr14:56592854
|
T | C | 2 | a0001c0001t0001g0130a0001c0001t0001g0173 | 2 | NA18999.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.344+6942T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56592854 | ||||||
chr14:56592943
|
G | A | 1 | a0001c0002t0001g0033 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.344+7031G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56592943 | ||||||
chr14:56593071
|
A | G | 2 | a0001c0001t0001g0121a0007c0012t0001g0120 | 2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.344+7159A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593071 | ||||||
chr14:56593280
|
T | TA | 15 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(12): Show | 17 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.344+7369dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593280 | |||||
chr14:56593422
|
G | A | 179 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(176): Show | 193 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.344+7510G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593422 | ||||||
chr14:56593491
|
A | G | 1 | a0001c0001t0005g0334 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.344+7579A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593491 | ||||||
chr14:56593529
|
C | T | 2 | a0001c0004t0003g0305a0001c0004t0003g0306 | 2 | NA18963.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.344+7617C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593529 | ||||||
chr14:56593566
|
G | A | 1 | a0001c0002t0001g0034 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.344+7654G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593566 | ||||||
chr14:56593593
|
G | A | 5 | a0001c0001t0009g0194a0001c0001t0009g0195a0001c0001t0009g0196others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+7681G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593593 | ||||||
chr14:56593659
|
G | A | 1 | a0004c0008t0004g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.344+7747G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593659 | ||||||
chr14:56593677
|
C | CT | 61 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(58): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.344+7793dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | |||||
chr14:56593677
|
C | CTT | 49 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0130others(46): Show | 53 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.344+7792_344+7793d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | |||||
chr14:56593677
|
C | CTTT | 7 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0159others(4): Show | 8 | HG02258.hp2 HG02683.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.344+7791_344+7793d others(5): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | |||||
chr14:56593677
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0005g0325 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.344+7782_344+7793d others(14): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | |||||
chr14:56593677
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0005g0326a0001c0001t0005g0327 | 2 | NA19078.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.344+7780_344+7793d others(16): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | |||||
chr14:56593677
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0008g0322a0001c0001t0025g0328 | 2 | HG02040.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.344+7779_344+7793d others(17): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | |||||
chr14:56593677
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0008g0323 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.344+7775_344+7793d others(21): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | |||||
chr14:56593677
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0005g0334 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.344+7774_344+7793d others(22): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | |||||
chr14:56593677
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0005g0324 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.344+7769_344+7793d others(27): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | |||||
chr14:56593677
|
C | CTTTTTTT others(22): Show |
1 | a0001c0001t0005g0333 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.344+7793_344+7794i others(31): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | |||||
chr14:56593677
|
CT | C | 89 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0005g0329others(86): Show | 100 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.344+7793delT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | |||||
chr14:56593677
|
CTTTTTTT others(4): Show |
C | 4 | a0001c0004t0016g0304a0002c0006t0003g0303a0002c0006t0003g0315others(1): Show | 4 | HG02738.hp1 NA19065.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.344+7783_344+7793d others(13): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | |||||
chr14:56593677
|
CTTTTTTT others(5): Show |
C | 52 | a0001c0001t0002g0278a0001c0004t0003g0295a0001c0004t0003g0296others(49): Show | 55 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.344+7782_344+7793d others(14): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | |||||
chr14:56593677
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0004t0003g0281a0004c0008t0005g0251 | 2 | HG01433.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.344+7781_344+7793d others(15): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | |||||
chr14:56593711
|
T | G | 122 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(119): Show | 133 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.344+7799T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593711 | ||||||
chr14:56593756
|
C | T | 2 | a0004c0008t0004g0128a0004c0008t0004g0129 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.344+7844C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593756 | ||||||
chr14:56593983
|
G | A | 1 | a0001c0011t0001g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.344+8071G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593983 | ||||||
chr14:56594016
|
G | A | 4 | a0001c0001t0006g0245a0001c0001t0006g0246a0001c0001t0006g0247others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+8104G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594016 | ||||||
chr14:56594050
|
A | T | 1 | a0001c0002t0001g0077 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.344+8138A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594050 | ||||||
chr14:56594099
|
A | G | 1 | a0002c0005t0001g0275 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.344+8187A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594099 | ||||||
chr14:56594165
|
T | G | 311 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(308): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.344+8253T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594165 | ||||||
chr14:56594171
|
T | C | 311 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(308): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.344+8259T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594171 | ||||||
chr14:56594172
|
T | C | 1 | a0003c0007t0013g0259 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.344+8260T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594172 | ||||||
chr14:56594214
|
T | C | 1 | a0002c0005t0002g0319 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.344+8302T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594214 | ||||||
chr14:56594218
|
A | G | 1 | a0002c0006t0003g0302 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.344+8306A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594218 | ||||||
chr14:56594231
|
T | C | 57 | a0001c0001t0002g0278a0001c0004t0003g0281a0001c0004t0003g0295others(54): Show | 60 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.344+8319T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594231 | ||||||
chr14:56594237
|
C | G | 105 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(102): Show | 116 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.344+8325C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594237 | ||||||
chr14:56594240
|
G | GTTAAAAT others(10): Show |
1 | a0001c0002t0001g0026 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.344+8334_344+8350d others(19): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56594240 | |||||
chr14:56594316
|
A | G | 3 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0091 | 3 | HG00639.hp1 HG00738.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.344+8404A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594316 | ||||||
chr14:56594455
|
T | A | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.344+8543T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594455 | ||||||
chr14:56594464
|
A | G | 41 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(38): Show | 42 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.344+8552A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594464 | ||||||
chr14:56594550
|
T | C | 1 | a0001c0001t0009g0199 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.344+8638T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594550 | ||||||
chr14:56594577
|
G | A | 1 | a0002c0003t0007g0032 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.344+8665G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594577 | ||||||
chr14:56594737
|
C | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG03491.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.344+8825C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594737 | ||||||
chr14:56594820
|
T | G | 26 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(23): Show | 29 | HG00438.hp2 HG00609.hp1 HG02027.hp2 others(26): Show |
intron_variant | MODIFIER | c.344+8908T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594820 | ||||||
chr14:56595202
|
A | G | 1 | a0002c0005t0012g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.345-8613A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595202 | ||||||
chr14:56595207
|
T | C | 1 | a0003c0007t0006g0267 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.345-8608T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595207 | ||||||
chr14:56595210
|
T | C | 1 | a0010c0016t0001g0092 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.345-8605T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595210 | ||||||
chr14:56595280
|
G | A | 302 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(299): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.345-8535G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595280 | ||||||
chr14:56595304
|
A | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0153others(1): Show | 6 | NA18951.hp1 NA18956.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-8511A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595304 | ||||||
chr14:56595336
|
A | G | 1 | a0003c0007t0001g0265 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.345-8479A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595336 | ||||||
chr14:56595449
|
G | C | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.345-8366G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595449 | ||||||
chr14:56595457
|
A | T | 1 | a0001c0004t0004g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.345-8358A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595457 | ||||||
chr14:56595489
|
C | A | 1 | a0001c0004t0004g0184 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.345-8326C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595489 | ||||||
chr14:56595566
|
A | G | 1 | a0002c0005t0001g0275 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.345-8249A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595566 | ||||||
chr14:56595624
|
C | T | 7 | a0002c0005t0001g0011a0002c0005t0001g0012a0002c0005t0001g0170others(4): Show | 9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-8191C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595624 | ||||||
chr14:56595625
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.345-8190A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595625 | ||||||
chr14:56595717
|
A | C | 60 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0122others(57): Show | 66 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.345-8098A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595717 | ||||||
chr14:56595966
|
A | G | 2 | a0001c0001t0002g0278a0001c0004t0014g0017 | 3 | HG02559.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.345-7849A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595966 | ||||||
chr14:56596013
|
A | C | 1 | a0002c0005t0001g0275 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.345-7802A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596013 | ||||||
chr14:56596190
|
T | C | 131 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0005g0324others(128): Show | 142 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.345-7625T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596190 | ||||||
chr14:56596269
|
G | A | 6 | a0001c0001t0006g0244a0001c0001t0006g0245a0001c0001t0006g0246others(3): Show | 6 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-7546G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596269 | ||||||
chr14:56596381
|
A | AGAGT | 15 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(12): Show | 15 | HG00639.hp2 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.345-7433_345-7432i others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | |||||
chr14:56596381
|
A | AGAGTGT | 27 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(24): Show | 30 | HG00438.hp2 HG00609.hp1 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.345-7433_345-7432i others(8): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | |||||
chr14:56596381
|
A | AGAGTGTG others(1): Show |
9 | a0001c0001t0002g0122a0001c0001t0002g0203a0001c0001t0002g0204others(6): Show | 10 | HG00099.hp2 HG00140.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-7433_345-7432i others(10): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | |||||
chr14:56596381
|
A | AGAGTGTG others(3): Show |
4 | a0001c0001t0002g0200a0001c0001t0002g0224a0001c0001t0002g0238others(1): Show | 4 | HG01123.hp1 HG02683.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-7433_345-7432i others(12): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | |||||
chr14:56596381
|
A | AGAGTGTG others(5): Show |
35 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0123others(32): Show | 40 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.345-7433_345-7432i others(14): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | |||||
chr14:56596381
|
A | AGAGTGTG others(7): Show |
8 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0223others(5): Show | 8 | HG01071.hp2 HG01358.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-7433_345-7432i others(16): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | |||||
chr14:56596381
|
A | AGT | 77 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0022others(74): Show | 86 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.345-7409_345-7408d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | |||||
chr14:56596381
|
A | AGTGT | 25 | a0001c0001t0008g0124a0001c0001t0008g0125a0001c0002t0001g0058others(22): Show | 25 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.345-7411_345-7408d others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | |||||
chr14:56596381
|
A | AGTGTGT | 8 | a0001c0002t0001g0074a0002c0003t0001g0098a0002c0006t0003g0279others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.345-7413_345-7408d others(8): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | |||||
chr14:56596381
|
A | AGTGTGTG others(1): Show |
22 | a0001c0002t0001g0021a0001c0004t0003g0281a0001c0004t0003g0295others(19): Show | 22 | HG00609.hp2 HG03239.hp1 HG03453.hp1 others(19): Show |
intron_variant | MODIFIER | c.345-7415_345-7408d others(10): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | |||||
chr14:56596381
|
A | AGTGTGTG others(3): Show |
4 | a0001c0004t0011g0310a0001c0004t0014g0017a0001c0004t0016g0304others(1): Show | 5 | HG02738.hp1 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-7417_345-7408d others(12): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | |||||
chr14:56596381
|
A | AGTGTGTG others(5): Show |
3 | a0001c0004t0011g0311a0001c0004t0011g0312a0001c0020t0011g0313 | 3 | HG01433.hp1 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.345-7419_345-7408d others(14): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | |||||
chr14:56596381
|
A | AGTGTGTG others(7): Show |
1 | a0001c0004t0015g0314 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.345-7421_345-7408d others(16): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | |||||
chr14:56596381
|
AGT | A | 3 | a0002c0005t0012g0132a0002c0005t0012g0133a0003c0007t0001g0269 | 3 | HG02572.hp1 HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.345-7409_345-7408d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | |||||
chr14:56596381
|
AGTGT | A | 3 | a0002c0005t0012g0174a0003c0007t0001g0252a0003c0007t0022g0260 | 3 | HG02970.hp2 HG03139.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.345-7411_345-7408d others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | |||||
chr14:56596383
|
T | A | 20 | a0001c0001t0001g0121a0001c0001t0006g0244a0001c0001t0006g0245others(17): Show | 22 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.345-7432T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596383 | ||||||
chr14:56596383
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.345-7432T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596383 | ||||||
chr14:56596385
|
T | A | 2 | a0002c0005t0012g0132a0002c0005t0012g0133 | 2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.345-7430T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596385 | ||||||
chr14:56596387
|
T | A | 1 | a0002c0005t0012g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.345-7428T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596387 | ||||||
chr14:56596396
|
G | A | 2 | a0004c0008t0005g0251a0004c0008t0005g0268 | 2 | HG01433.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.345-7419G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596396 | ||||||
chr14:56596402
|
G | A | 1 | a0002c0005t0012g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.345-7413G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596402 | ||||||
chr14:56596404
|
G | A | 3 | a0002c0005t0012g0131a0002c0005t0012g0132a0002c0005t0012g0133 | 3 | HG03017.hp1 HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.345-7411G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596404 | ||||||
chr14:56596406
|
G | A | 12 | a0001c0001t0001g0121a0002c0005t0001g0011a0002c0005t0001g0012others(9): Show | 14 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-7409G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596406 | ||||||
chr14:56596406
|
G | GTGTGTA | 3 | a0001c0001t0008g0126a0001c0001t0008g0127a0002c0003t0001g0064 | 3 | NA18943.hp2 NA18979.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.345-7408_345-7407i others(8): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596406 | |||||
chr14:56596406
|
G | GTGTGTGT others(5): Show |
4 | a0001c0001t0005g0329a0001c0001t0005g0330a0001c0001t0005g0331others(1): Show | 4 | HG00621.hp1 NA18945.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-7408_345-7407i others(14): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596406 | |||||
chr14:56596406
|
G | GTGTGTGT others(5): Show |
9 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(6): Show | 9 | HG01358.hp2 HG02040.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-7408_345-7407i others(14): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596406 | |||||
chr14:56596406
|
G | GTGTGTGT others(21): Show |
1 | a0001c0011t0001g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.345-7408_345-7407i others(30): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596406 | |||||
chr14:56596406
|
G | GTGTGTGT others(7): Show |
1 | a0001c0001t0025g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.345-7408_345-7407i others(16): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596406 | |||||
chr14:56596408
|
A | G | 189 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(186): Show | 206 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.345-7407A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596408 | ||||||
chr14:56596410
|
A | G | 77 | a0001c0001t0001g0167a0001c0002t0001g0002a0001c0002t0001g0023others(74): Show | 84 | HG00099.hp1 HG00609.hp2 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.345-7405A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596410 | ||||||
chr14:56596412
|
A | G | 12 | a0001c0004t0003g0281a0001c0004t0003g0301a0001c0004t0003g0306others(9): Show | 14 | HG01433.hp1 HG02015.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.345-7403A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596412 | ||||||
chr14:56596414
|
A | G | 1 | a0001c0004t0003g0306 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.345-7401A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596414 | ||||||
chr14:56596422
|
A | G | 1 | a0002c0006t0003g0300 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.345-7393A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596422 | ||||||
chr14:56596423
|
T | C | 9 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0002g0220others(6): Show | 9 | HG01071.hp2 HG02896.hp2 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-7392T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596423 | ||||||
chr14:56596423
|
T | TAC | 43 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0201others(40): Show | 49 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.345-7391_345-7390i others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596423 | |||||
chr14:56596423
|
TATAC | T | 8 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(5): Show | 8 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.345-7386_345-7383d others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596423 | |||||
chr14:56596425
|
T | C | 98 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(95): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.345-7390T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596425 | ||||||
chr14:56596425
|
T | TACAC | 12 | a0001c0001t0002g0200a0001c0001t0002g0224a0001c0001t0002g0238others(9): Show | 12 | HG01123.hp1 HG01891.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-7387_345-7386i others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596425 | |||||
chr14:56596425
|
T | TATAC | 7 | a0002c0005t0001g0011a0002c0005t0001g0012a0002c0005t0001g0168others(4): Show | 9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-7389_345-7388i others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596425 | |||||
chr14:56596425
|
TAC | T | 6 | a0001c0002t0001g0078a0002c0003t0001g0192a0002c0003t0001g0193others(3): Show | 6 | HG02135.hp1 HG03540.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-7388_345-7387d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596425 | |||||
chr14:56596427
|
C | T | 155 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(152): Show | 169 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.345-7388C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596427 | ||||||
chr14:56596429
|
T | C | 123 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(120): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.345-7386T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596429 | ||||||
chr14:56596541
|
T | C | 189 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0005g0324others(186): Show | 203 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.345-7274T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596541 | ||||||
chr14:56596560
|
A | G | 60 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0122others(57): Show | 66 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.345-7255A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596560 | ||||||
chr14:56596569
|
C | G | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.345-7246C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596569 | ||||||
chr14:56596618
|
C | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0155 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.345-7197C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596618 | ||||||
chr14:56596695
|
G | A | 2 | a0001c0001t0008g0126a0001c0004t0004g0184 | 2 | HG03195.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.345-7120G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596695 | ||||||
chr14:56596767
|
C | CA | 109 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(106): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.345-7033dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596767 | |||||
chr14:56596782
|
A | AAT | 10 | a0001c0001t0001g0121a0001c0001t0001g0145a0001c0001t0001g0146others(7): Show | 10 | HG00438.hp2 HG02258.hp2 HG03017.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-7033_345-7032i others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596782 | ||||||
chr14:56596782
|
A | G | 2 | a0002c0006t0003g0285a0002c0006t0003g0286 | 2 | NA18965.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.345-7033A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596782 | ||||||
chr14:56596782
|
A | T | 1 | a0001c0004t0003g0305 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.345-7033A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596782 | ||||||
chr14:56596783
|
T | A | 1 | a0001c0001t0001g0147 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.345-7032T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596783 | ||||||
chr14:56596784
|
T | A | 11 | a0001c0001t0001g0121a0001c0001t0001g0145a0001c0001t0001g0146others(8): Show | 11 | HG00438.hp2 HG02258.hp2 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-7031T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596784 | ||||||
chr14:56596784
|
T | TA | 16 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(13): Show | 16 | HG00621.hp1 HG02040.hp2 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.345-7020dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596784 | |||||
chr14:56596784
|
T | TAA | 15 | a0001c0002t0001g0037a0001c0002t0001g0043a0001c0002t0001g0052others(12): Show | 15 | HG01993.hp2 HG03017.hp2 HG03195.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-7021_345-7020d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596784 | |||||
chr14:56596784
|
T | TAAA | 86 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(83): Show | 97 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.345-7022_345-7020d others(5): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596784 | |||||
chr14:56596785
|
A | T | 1 | a0001c0001t0001g0147 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.345-7030A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596785 | ||||||
chr14:56596794
|
A | AAAAAAAA others(3): Show |
3 | a0001c0004t0004g0182a0001c0004t0004g0185a0001c0004t0004g0191 | 3 | HG01243.hp2 HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.345-7020_345-7019i others(12): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596794 | |||||
chr14:56596794
|
A | AAAAAATA others(3): Show |
8 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0183others(5): Show | 10 | HG01081.hp2 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-7020_345-7019i others(12): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596794 | |||||
chr14:56596794
|
A | AAAAAATA others(5): Show |
1 | a0001c0004t0004g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.345-7020_345-7019i others(14): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596794 | |||||
chr14:56596794
|
A | AAAAATAT others(4): Show |
1 | a0001c0004t0004g0184 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.345-7020_345-7019i others(13): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596794 | |||||
chr14:56596794
|
A | AAAAATAT others(6): Show |
1 | a0004c0008t0004g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.345-7020_345-7019i others(15): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596794 | |||||
chr14:56596794
|
A | AAAATATA others(7): Show |
1 | a0001c0004t0004g0181 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.345-7020_345-7019i others(16): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596794 | |||||
chr14:56596794
|
A | AT | 50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(47): Show | 55 | HG00639.hp2 HG01109.hp1 HG01496.hp2 others(52): Show |
intron_variant | MODIFIER | c.345-7021_345-7020i others(3): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596794 | ||||||
chr14:56596794
|
A | T | 60 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0122others(57): Show | 66 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.345-7021A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596794 | ||||||
chr14:56596795
|
A | AAAATG | 39 | a0001c0001t0002g0278a0001c0004t0003g0281a0001c0004t0003g0295others(36): Show | 40 | HG01070.hp1 HG01071.hp1 HG01433.hp1 others(37): Show |
intron_variant | MODIFIER | c.345-7020_345-7019i others(7): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596795 | ||||||
chr14:56596796
|
T | A | 99 | a0001c0001t0008g0124a0001c0001t0008g0125a0001c0001t0008g0126others(96): Show | 110 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.345-7019T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596796 | ||||||
chr14:56596808
|
C | T | 170 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0278others(167): Show | 184 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.345-7007C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596808 | ||||||
chr14:56596871
|
G | T | 1 | a0002c0003t0001g0098 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.345-6944G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596871 | ||||||
chr14:56597152
|
A | T | 2 | a0001c0001t0009g0194a0001c0001t0009g0197 | 2 | HG01891.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.345-6663A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56597152 | ||||||
chr14:56597257
|
A | G | 41 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(38): Show | 42 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.345-6558A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56597257 | ||||||
chr14:56597293
|
A | G | 1 | a0001c0001t0002g0237 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.345-6522A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56597293 | ||||||
chr14:56597435
|
C | T | 1 | a0001c0002t0001g0107 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.345-6380C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56597435 | ||||||
chr14:56597568
|
A | G | 15 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(12): Show | 17 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.345-6247A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56597568 | ||||||
chr14:56597584
|
G | A | 1 | a0002c0003t0017g0318 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.345-6231G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56597584 | ||||||
chr14:56597604
|
G | A | 2 | a0004c0008t0004g0128a0004c0008t0004g0129 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.345-6211G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56597604 | ||||||
chr14:56597651
|
G | T | 121 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(118): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.345-6164G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56597651 | ||||||
chr14:56598139
|
C | G | 1 | a0001c0002t0001g0073 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.345-5676C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56598139 | ||||||
chr14:56598148
|
G | A | 56 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(53): Show | 59 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.345-5667G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56598148 | ||||||
chr14:56598601
|
T | C | 9 | a0003c0007t0001g0249a0003c0007t0001g0250a0003c0007t0001g0253others(6): Show | 9 | HG00140.hp1 HG00735.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-5214T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56598601 | ||||||
chr14:56598625
|
A | G | 9 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(6): Show | 9 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-5190A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56598625 | ||||||
chr14:56598819
|
T | C | 1 | a0010c0016t0001g0092 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.345-4996T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56598819 | ||||||
chr14:56598892
|
A | C | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.345-4923A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56598892 | ||||||
chr14:56598955
|
G | A | 1 | a0004c0008t0004g0129 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.345-4860G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56598955 | ||||||
chr14:56599056
|
T | C | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-4759T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599056 | ||||||
chr14:56599225
|
G | A | 1 | a0002c0006t0003g0308 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.345-4590G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599225 | ||||||
chr14:56599342
|
T | C | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.345-4473T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599342 | ||||||
chr14:56599449
|
A | G | 57 | a0001c0001t0002g0278a0001c0004t0003g0281a0001c0004t0003g0295others(54): Show | 60 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.345-4366A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599449 | ||||||
chr14:56599516
|
T | C | 10 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(7): Show | 10 | HG00639.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-4299T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599516 | ||||||
chr14:56599969
|
G | C | 1 | a0001c0002t0001g0096 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.345-3846G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599969 | ||||||
chr14:56599974
|
G | T | 1 | a0001c0002t0001g0072 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.345-3841G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599974 | ||||||
chr14:56599981
|
A | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0155 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.345-3834A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599981 | ||||||
chr14:56599990
|
C | G | 1 | a0003c0007t0001g0252 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.345-3825C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599990 | ||||||
chr14:56600002
|
T | C | 3 | a0001c0001t0001g0276a0001c0001t0001g0277a0002c0005t0001g0275 | 3 | HG02257.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.345-3813T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600002 | ||||||
chr14:56600027
|
A | G | 1 | a0003c0007t0001g0252 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.345-3788A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600027 | ||||||
chr14:56600096
|
T | G | 1 | a0003c0007t0001g0265 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.345-3719T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600096 | ||||||
chr14:56600122
|
A | G | 3 | a0001c0001t0006g0244a0004c0008t0004g0128a0004c0008t0004g0129 | 3 | HG02280.hp2 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.345-3693A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600122 | ||||||
chr14:56600190
|
C | T | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-3625C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600190 | ||||||
chr14:56600212
|
C | T | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-3603C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600212 | ||||||
chr14:56600260
|
G | A | 310 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(307): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.345-3555G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600260 | ||||||
chr14:56600264
|
G | A | 6 | a0001c0001t0006g0244a0001c0001t0006g0245a0001c0001t0006g0246others(3): Show | 6 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-3551G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600264 | ||||||
chr14:56600279
|
T | C | 57 | a0001c0001t0002g0278a0001c0004t0003g0281a0001c0004t0003g0295others(54): Show | 60 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.345-3536T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600279 | ||||||
chr14:56600282
|
C | T | 1 | a0003c0007t0001g0256 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.345-3533C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600282 | ||||||
chr14:56600406
|
G | A | 1 | a0001c0001t0009g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.345-3409G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600406 | ||||||
chr14:56600610
|
C | G | 56 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0122others(53): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.345-3205C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600610 | ||||||
chr14:56600652
|
A | G | 1 | a0002c0005t0012g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.345-3163A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600652 | ||||||
chr14:56600748
|
C | G | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.345-3067C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600748 | ||||||
chr14:56600977
|
C | A | 85 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0005g0324others(82): Show | 88 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.345-2838C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600977 | ||||||
chr14:56601006
|
G | A | 56 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(53): Show | 59 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.345-2809G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601006 | ||||||
chr14:56601084
|
A | G | 8 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(5): Show | 8 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.345-2731A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601084 | ||||||
chr14:56601135
|
T | G | 2 | a0001c0002t0001g0043a0001c0002t0001g0080 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.345-2680T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601135 | ||||||
chr14:56601152
|
T | G | 1 | a0001c0004t0004g0189 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.345-2663T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601152 | ||||||
chr14:56601157
|
C | T | 56 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(53): Show | 59 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.345-2658C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601157 | ||||||
chr14:56601220
|
T | C | 8 | a0002c0005t0001g0011a0002c0005t0001g0012a0002c0005t0001g0168others(5): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-2595T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601220 | ||||||
chr14:56601228
|
C | G | 5 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(2): Show | 5 | HG02809.hp2 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-2587C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601228 | ||||||
chr14:56601253
|
G | C | 1 | a0001c0011t0001g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.345-2562G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601253 | ||||||
chr14:56601294
|
T | C | 1 | a0001c0002t0001g0052 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.345-2521T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601294 | ||||||
chr14:56601436
|
T | C | 1 | a0001c0001t0002g0226 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.345-2379T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601436 | ||||||
chr14:56601523
|
A | G | 56 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(53): Show | 59 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.345-2292A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601523 | ||||||
chr14:56601847
|
C | T | 1 | a0001c0004t0014g0017 | 2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.345-1968C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601847 | ||||||
chr14:56601871
|
C | T | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-1944C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601871 | ||||||
chr14:56601895
|
C | T | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-1920C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601895 | ||||||
chr14:56601922
|
T | A | 1 | a0002c0003t0001g0093 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.345-1893T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601922 | ||||||
chr14:56601942
|
T | A | 56 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(53): Show | 59 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.345-1873T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601942 | ||||||
chr14:56601961
|
C | T | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-1854C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601961 | ||||||
chr14:56602077
|
A | G | 79 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0005g0324others(76): Show | 82 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.345-1738A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56602077 | ||||||
chr14:56602163
|
G | T | 310 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(307): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.345-1652G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56602163 | ||||||
chr14:56602214
|
A | G | 1 | a0001c0001t0005g0327 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.345-1601A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56602214 | ||||||
chr14:56602227
|
T | C | 1 | a0002c0003t0001g0057 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.345-1588T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56602227 | ||||||
chr14:56602348
|
G | T | 1 | a0002c0005t0002g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.345-1467G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56602348 | ||||||
chr14:56602557
|
T | C | 230 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(227): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.345-1258T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56602557 | ||||||
chr14:56602628
|
A | G | 4 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(1): Show | 4 | HG02809.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-1187A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56602628 | ||||||
chr14:56602746
|
C | CAG | 311 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(308): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.345-1068_345-1067i others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56602746 | |||||
chr14:56603254
|
G | GA | 224 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(221): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.345-553dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56603254 | |||||
chr14:56603358
|
A | G | 9 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(6): Show | 9 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-457A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56603358 | ||||||
chr14:56603586
|
T | G | 1 | a0010c0016t0001g0092 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.345-229T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56603586 | ||||||
chr14:56603689
|
A | G | 7 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(4): Show | 7 | HG01358.hp1 HG02559.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-126A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56603689 | ||||||
chr14:56603713
|
C | A | 13 | a0002c0006t0003g0284a0002c0006t0003g0285a0002c0006t0003g0286others(10): Show | 13 | NA18965.hp2 NA18979.hp2 NA18980.hp2 others(10): Show |
intron_variant | MODIFIER | c.345-102C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56603713 | ||||||
chr14:56603728
|
A | G | 1 | a0004c0008t0006g0114 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.345-87A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56603728 | ||||||
chr14:56603748
|
A | G | 1 | a0004c0008t0018g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.345-67A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56603748 | ||||||
chr14:56603783
|
A | G | 311 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(308): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.345-32A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56603783 | ||||||
chr14:56604091
|
A | T | 1 | a0001c0002t0001g0088 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.522+99A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604091 | ||||||
chr14:56604254
|
G | A | 6 | a0001c0001t0006g0244a0001c0001t0006g0245a0001c0001t0006g0246others(3): Show | 6 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.522+262G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604254 | ||||||
chr14:56604286
|
A | G | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.522+294A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604286 | ||||||
chr14:56604323
|
T | A | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.522+331T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604323 | ||||||
chr14:56604431
|
G | A | 1 | a0001c0011t0001g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.522+439G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604431 | ||||||
chr14:56604489
|
T | C | 1 | a0003c0007t0001g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.522+497T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604489 | ||||||
chr14:56604744
|
A | T | 1 | a0002c0005t0001g0168 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.522+752A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604744 | ||||||
chr14:56604751
|
A | G | 4 | a0001c0001t0008g0124a0001c0001t0008g0125a0001c0001t0008g0126others(1): Show | 4 | HG02523.hp1 NA18943.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+759A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604751 | ||||||
chr14:56604815
|
C | T | 298 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(295): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.523-755C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604815 | ||||||
chr14:56604859
|
G | C | 5 | a0001c0001t0006g0244a0001c0001t0006g0245a0001c0001t0006g0246others(2): Show | 5 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.523-711G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604859 | ||||||
chr14:56604929
|
T | A | 295 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(292): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.523-641T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604929 | ||||||
chr14:56605108
|
C | T | 1 | a0010c0016t0001g0092 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.523-462C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605108 | ||||||
chr14:56605180
|
G | C | 1 | a0003c0007t0022g0260 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.523-390G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605180 | ||||||
chr14:56605262
|
G | A | 1 | a0003c0007t0001g0016 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.523-308G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605262 | ||||||
chr14:56605444
|
C | T | 1 | a0001c0004t0016g0304 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.523-126C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605444 | ||||||
chr14:56605467
|
C | CTT | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.523-103_523-102ins others(2): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605467 | ||||||
chr14:56605471
|
A | G | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.523-99A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605471 | ||||||
chr14:56605476
|
A | G | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.523-94A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605476 | ||||||
chr14:56605485
|
T | A | 144 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 158 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.523-85T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605485 | ||||||
chr14:56605544
|
A | AG | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.523-26_523-25insG | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605544 | ||||||
chr14:56605545
|
A | T | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.523-25A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605545 | ||||||
chr14:56605703
|
A | G | 1 | a0001c0001t0002g0207 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.636+20A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56605703 | ||||||
chr14:56605799
|
A | G | 2 | a0003c0007t0001g0258a0003c0007t0022g0260 | 2 | HG02698.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.636+116A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56605799 | ||||||
chr14:56605923
|
T | G | 2 | a0001c0002t0001g0065a0001c0002t0001g0067 | 2 | NA18957.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.636+240T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56605923 | ||||||
chr14:56605925
|
A | C | 41 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(38): Show | 42 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.636+242A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56605925 | ||||||
chr14:56605941
|
A | T | 1 | a0002c0003t0001g0099 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.636+258A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56605941 | ||||||
chr14:56605975
|
C | T | 55 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(52): Show | 58 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.636+292C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56605975 | ||||||
chr14:56606107
|
G | A | 1 | a0001c0002t0001g0072 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.636+424G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56606107 | ||||||
chr14:56606263
|
T | C | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.636+580T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56606263 | ||||||
chr14:56606281
|
T | C | 314 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(311): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.636+598T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56606281 | ||||||
chr14:56606564
|
A | G | 311 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(308): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.636+881A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56606564 | ||||||
chr14:56606759
|
G | A | 14 | a0002c0005t0001g0011a0002c0005t0001g0012a0002c0005t0001g0168others(11): Show | 16 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.636+1076G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56606759 | ||||||
chr14:56606770
|
C | G | 55 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(52): Show | 58 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.636+1087C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56606770 | ||||||
chr14:56606833
|
T | C | 41 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(38): Show | 42 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.636+1150T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56606833 | ||||||
chr14:56606928
|
A | G | 146 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(143): Show | 160 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.636+1245A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56606928 | ||||||
chr14:56607000
|
T | A | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.636+1317T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607000 | ||||||
chr14:56607081
|
A | G | 1 | a0014c0010t0001g0087 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.636+1398A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607081 | ||||||
chr14:56607084
|
G | A | 1 | a0012c0014t0024g0035 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.636+1401G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607084 | ||||||
chr14:56607154
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.636+1471A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607154 | ||||||
chr14:56607276
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.636+1593C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607276 | ||||||
chr14:56607485
|
C | T | 1 | a0003c0007t0001g0261 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.637-1621C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607485 | ||||||
chr14:56607584
|
C | T | 3 | a0004c0008t0004g0128a0004c0008t0004g0129a0004c0008t0004g0178 | 3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.637-1522C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607584 | ||||||
chr14:56607618
|
G | A | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-1488G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607618 | ||||||
chr14:56607620
|
G | A | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-1486G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607620 | ||||||
chr14:56607623
|
T | C | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-1483T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607623 | ||||||
chr14:56607625
|
T | A | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-1481T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607625 | ||||||
chr14:56607626
|
A | G | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-1480A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607626 | ||||||
chr14:56607627
|
T | C | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-1479T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607627 | ||||||
chr14:56607629
|
C | A | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-1477C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607629 | ||||||
chr14:56607658
|
A | G | 144 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 158 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.637-1448A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607658 | ||||||
chr14:56607712
|
G | A | 1 | a0001c0002t0001g0034 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.637-1394G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607712 | ||||||
chr14:56607712
|
G | GTA | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.637-1384_637-1383d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 56607712 | |||||
chr14:56607746
|
G | T | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-1360G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607746 | ||||||
chr14:56607802
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG02280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.637-1304G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607802 | ||||||
chr14:56607971
|
T | G | 4 | a0001c0001t0002g0203a0001c0001t0002g0208a0001c0001t0002g0227others(1): Show | 4 | HG00140.hp2 HG00733.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-1135T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607971 | ||||||
chr14:56608041
|
T | C | 14 | a0002c0005t0001g0011a0002c0005t0001g0012a0002c0005t0001g0168others(11): Show | 16 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.637-1065T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56608041 | ||||||
chr14:56608088
|
C | G | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-1018C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56608088 | ||||||
chr14:56608189
|
A | C | 1 | a0004c0008t0018g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.637-917A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56608189 | ||||||
chr14:56608304
|
G | A | 55 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(52): Show | 58 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.637-802G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56608304 | ||||||
chr14:56608636
|
T | TGTAGAAA others(6): Show |
1 | a0002c0003t0001g0081 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.637-469_637-457dup others(13): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 56608636 | |||||
chr14:56608694
|
AATG | A | 54 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0122others(51): Show | 60 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.637-404_637-402del others(3): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 56608694 | |||||
chr14:56609376
|
A | G | 1 | a0001c0004t0004g0187 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.816+91A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609376 | ||||||
chr14:56609453
|
A | T | 39 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0005g0324others(36): Show | 41 | HG00621.hp1 HG01358.hp2 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.816+168A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609453 | ||||||
chr14:56609544
|
T | C | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.816+259T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609544 | ||||||
chr14:56609550
|
C | T | 1 | a0001c0002t0001g0089 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.816+265C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609550 | ||||||
chr14:56609576
|
G | A | 4 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0223others(1): Show | 4 | HG01993.hp1 HG02148.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+291G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609576 | ||||||
chr14:56609678
|
A | C | 20 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(17): Show | 20 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.816+393A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609678 | ||||||
chr14:56609694
|
T | G | 1 | a0003c0007t0001g0252 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+409T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609694 | ||||||
chr14:56609811
|
A | G | 20 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(17): Show | 22 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.816+526A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609811 | ||||||
chr14:56609818
|
T | G | 2 | a0001c0002t0001g0109a0002c0003t0001g0110 | 2 | NA19010.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.816+533T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609818 | ||||||
chr14:56609932
|
A | T | 1 | a0003c0007t0001g0249 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.816+647A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609932 | ||||||
chr14:56609955
|
C | T | 1 | a0001c0001t0002g0204 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.816+670C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609955 | ||||||
chr14:56609958
|
T | G | 1 | a0001c0001t0009g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.816+673T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609958 | ||||||
chr14:56609959
|
T | C | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.816+674T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609959 | ||||||
chr14:56610032
|
A | G | 2 | a0001c0001t0006g0247a0001c0001t0006g0248 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.816+747A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610032 | ||||||
chr14:56610218
|
T | TA | 6 | a0001c0001t0006g0244a0001c0001t0006g0245a0001c0001t0006g0246others(3): Show | 6 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.816+941dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 56610218 | |||||
chr14:56610227
|
G | T | 3 | a0004c0008t0004g0128a0004c0008t0004g0129a0004c0008t0004g0178 | 3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.816+942G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610227 | ||||||
chr14:56610267
|
T | G | 39 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0005g0324others(36): Show | 41 | HG00621.hp1 HG01358.hp2 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.816+982T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610267 | ||||||
chr14:56610270
|
T | C | 1 | a0004c0008t0018g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.816+985T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610270 | ||||||
chr14:56610303
|
C | T | 2 | a0001c0001t0002g0218a0001c0001t0002g0222 | 2 | HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.816+1018C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610303 | ||||||
chr14:56610323
|
C | G | 1 | a0004c0008t0018g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.816+1038C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610323 | ||||||
chr14:56610385
|
C | T | 2 | a0001c0001t0001g0121a0007c0012t0001g0120 | 2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.816+1100C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610385 | ||||||
chr14:56610478
|
G | A | 1 | a0001c0004t0014g0017 | 2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.816+1193G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610478 | ||||||
chr14:56610501
|
C | G | 5 | a0001c0001t0009g0194a0001c0001t0009g0195a0001c0001t0009g0196others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+1216C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610501 | ||||||
chr14:56610508
|
C | T | 41 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(38): Show | 42 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.816+1223C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610508 | ||||||
chr14:56610531
|
C | T | 2 | a0001c0001t0001g0121a0007c0012t0001g0120 | 2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.816+1246C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610531 | ||||||
chr14:56610532
|
G | A | 1 | a0001c0002t0001g0028 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.816+1247G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610532 | ||||||
chr14:56610572
|
G | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(25): Show | 31 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.816+1287G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610572 | ||||||
chr14:56610947
|
TTTTC | T | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.817-1278_817-1275d others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 56610947 | |||||
chr14:56610951
|
C | G | 1 | a0001c0001t0002g0204 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.817-1294C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610951 | ||||||
chr14:56610963
|
C | CT | 6 | a0001c0001t0001g0277a0002c0005t0001g0011a0002c0005t0001g0012others(3): Show | 8 | HG01884.hp2 HG01891.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.817-1279dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 56610963 | |||||
chr14:56610966
|
TC | T | 40 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(37): Show | 41 | HG00609.hp2 HG01071.hp1 HG02015.hp1 others(38): Show |
intron_variant | MODIFIER | c.817-1278delC | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610966 | ||||||
chr14:56610967
|
C | CT | 7 | a0001c0001t0001g0154a0001c0001t0001g0163a0001c0001t0002g0229others(4): Show | 7 | HG02148.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-1261dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 56610967 | |||||
chr14:56610967
|
C | T | 24 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0006g0113others(21): Show | 26 | HG01433.hp1 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.817-1278C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610967 | ||||||
chr14:56610967
|
CT | C | 18 | a0001c0001t0006g0244a0001c0002t0001g0039a0001c0002t0001g0053others(15): Show | 20 | HG01081.hp2 HG01167.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.817-1261delT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 56610967 | |||||
chr14:56611006
|
A | G | 304 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(301): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.817-1239A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611006 | ||||||
chr14:56611006
|
A | T | 3 | a0001c0001t0002g0242a0001c0001t0010g0004a0001c0001t0010g0239 | 6 | HG02074.hp2 NA18942.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.817-1239A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611006 | ||||||
chr14:56611027
|
C | T | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.817-1218C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611027 | ||||||
chr14:56611256
|
G | A | 1 | a0001c0002t0001g0052 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.817-989G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611256 | ||||||
chr14:56611258
|
A | G | 1 | a0001c0002t0001g0052 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.817-987A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611258 | ||||||
chr14:56611306
|
A | G | 1 | a0002c0005t0012g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.817-939A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611306 | ||||||
chr14:56611354
|
C | G | 1 | a0001c0004t0004g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.817-891C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611354 | ||||||
chr14:56611387
|
G | T | 5 | a0001c0001t0009g0194a0001c0001t0009g0195a0001c0001t0009g0196others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-858G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611387 | ||||||
chr14:56611447
|
G | A | 19 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(16): Show | 19 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.817-798G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611447 | ||||||
chr14:56611594
|
T | C | 19 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(16): Show | 19 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.817-651T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611594 | ||||||
chr14:56611741
|
A | G | 2 | a0002c0003t0001g0030a0002c0003t0001g0031 | 2 | NA18956.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.817-504A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611741 | ||||||
chr14:56611758
|
A | G | 1 | a0001c0002t0001g0052 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.817-487A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611758 | ||||||
chr14:56611917
|
C | T | 1 | a0003c0007t0001g0272 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.817-328C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611917 | ||||||
chr14:56612525
|
A | G | 14 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(11): Show | 16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.857+240A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56612525 | ||||||
chr14:56612585
|
T | C | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.857+300T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56612585 | ||||||
chr14:56612699
|
C | CT | 22 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(19): Show | 22 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.857+431dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56612699 | |||||
chr14:56612699
|
CT | C | 8 | a0001c0001t0009g0195a0001c0002t0001g0037a0001c0002t0001g0065others(5): Show | 8 | HG01167.hp2 HG02615.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.857+431delT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56612699 | |||||
chr14:56612699
|
CTT | C | 55 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(52): Show | 58 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.857+430_857+431del others(2): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56612699 | |||||
chr14:56612777
|
T | A | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.857+492T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56612777 | ||||||
chr14:56612793
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.857+508C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56612793 | ||||||
chr14:56612799
|
C | T | 14 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(11): Show | 16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.857+514C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56612799 | ||||||
chr14:56612839
|
G | A | 4 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0091others(1): Show | 4 | HG00639.hp1 HG00738.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.857+554G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56612839 | ||||||
chr14:56612973
|
T | C | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.857+688T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56612973 | ||||||
chr14:56613254
|
T | C | 2 | a0003c0007t0001g0249a0003c0007t0001g0250 | 2 | HG01175.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.857+969T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613254 | ||||||
chr14:56613513
|
A | G | 2 | a0001c0004t0004g0180a0001c0004t0004g0181 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.857+1228A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613513 | ||||||
chr14:56613545
|
C | T | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.857+1260C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613545 | ||||||
chr14:56613741
|
A | T | 14 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(11): Show | 16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.857+1456A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613741 | ||||||
chr14:56613787
|
C | T | 1 | a0001c0002t0001g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.857+1502C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613787 | ||||||
chr14:56613791
|
G | A | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.857+1506G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613791 | ||||||
chr14:56613894
|
G | A | 3 | a0004c0008t0004g0128a0004c0008t0004g0129a0004c0008t0004g0178 | 3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.857+1609G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613894 | ||||||
chr14:56613895
|
C | CA | 202 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(199): Show | 217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.857+1625dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56613895 | |||||
chr14:56613895
|
C | CAA | 10 | a0001c0001t0002g0220a0001c0001t0010g0239a0001c0004t0004g0181others(7): Show | 10 | HG00609.hp2 HG00735.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.857+1624_857+1625d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56613895 | |||||
chr14:56613895
|
C | CAAAAAAA others(14): Show |
4 | a0001c0001t0005g0325a0001c0001t0005g0327a0001c0001t0005g0329others(1): Show | 4 | NA18945.hp2 NA18959.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.857+1625_857+1626i others(23): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56613895 | |||||
chr14:56613895
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0005g0331 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857+1625_857+1626i others(24): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56613895 | |||||
chr14:56613895
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0005g0330 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.857+1625_857+1626i others(25): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56613895 | |||||
chr14:56613910
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0005g0334 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.857+1625_857+1626i others(29): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613910 | ||||||
chr14:56613910
|
A | AAAAAAAA others(15): Show |
3 | a0001c0001t0005g0326a0001c0001t0008g0322a0001c0001t0008g0323 | 3 | HG02040.hp2 NA19009.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.857+1625_857+1626i others(24): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613910 | ||||||
chr14:56613910
|
A | AAAAAAAA others(14): Show |
3 | a0001c0001t0005g0324a0001c0001t0008g0321a0001c0001t0025g0328 | 3 | HG02738.hp2 NA18967.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.857+1625_857+1626i others(23): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613910 | ||||||
chr14:56613910
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0005g0333 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.857+1625_857+1626i others(22): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613910 | ||||||
chr14:56613910
|
A | AAAAAAAA others(10): Show |
3 | a0001c0001t0008g0124a0001c0001t0008g0125a0001c0001t0008g0127 | 3 | HG02523.hp1 NA18943.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.857+1625_857+1626i others(19): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613910 | ||||||
chr14:56613910
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0008g0126 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.857+1625_857+1626i others(18): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613910 | ||||||
chr14:56613988
|
C | T | 4 | a0001c0001t0008g0124a0001c0001t0008g0125a0001c0001t0008g0126others(1): Show | 4 | HG02523.hp1 NA18943.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.857+1703C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613988 | ||||||
chr14:56613989
|
G | A | 1 | a0013c0013t0001g0171 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.857+1704G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613989 | ||||||
chr14:56614022
|
C | T | 1 | a0002c0005t0012g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.857+1737C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56614022 | ||||||
chr14:56614219
|
T | TA | 109 | a0001c0001t0001g0121a0001c0001t0001g0276a0001c0001t0001g0277others(106): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.858-1707dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56614219 | |||||
chr14:56614219
|
TA | T | 50 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0200others(47): Show | 55 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.858-1707delA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56614219 | |||||
chr14:56614295
|
G | A | 55 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(52): Show | 58 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.858-1649G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56614295 | ||||||
chr14:56614597
|
A | G | 3 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0222 | 3 | HG00280.hp2 HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.858-1347A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56614597 | ||||||
chr14:56614648
|
C | T | 1 | a0014c0010t0001g0087 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.858-1296C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56614648 | ||||||
chr14:56614655
|
A | G | 1 | a0002c0005t0001g0275 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.858-1289A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56614655 | ||||||
chr14:56614724
|
CTTCTGTG | C | 74 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(71): Show | 77 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(74): Show |
intron_variant | MODIFIER | c.858-1211_858-1205d others(9): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56614724 | |||||
chr14:56615127
|
T | G | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00639.hp2 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.858-817T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615127 | ||||||
chr14:56615209
|
C | G | 1 | a0001c0002t0001g0106 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.858-735C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615209 | ||||||
chr14:56615377
|
A | G | 1 | a0014c0010t0001g0087 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.858-567A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615377 | ||||||
chr14:56615383
|
A | G | 1 | a0001c0002t0001g0106 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.858-561A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615383 | ||||||
chr14:56615412
|
G | A | 1 | a0003c0007t0001g0270 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.858-532G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615412 | ||||||
chr14:56615414
|
T | A | 1 | a0003c0007t0001g0270 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.858-530T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615414 | ||||||
chr14:56615415
|
T | G | 1 | a0003c0007t0001g0270 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.858-529T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615415 | ||||||
chr14:56615416
|
T | A | 1 | a0003c0007t0001g0270 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.858-528T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615416 | ||||||
chr14:56615500
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.858-444C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615500 | ||||||
chr14:56615577
|
T | C | 1 | a0002c0003t0001g0082 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.858-367T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615577 | ||||||
chr14:56615731
|
G | A | 2 | a0002c0005t0002g0013a0002c0005t0002g0230 | 3 | HG00099.hp2 HG01934.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.858-213G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615731 | ||||||
chr14:56615757
|
C | T | 1 | a0001c0011t0001g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.858-187C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615757 | ||||||
chr14:56615885
|
T | G | 5 | a0001c0001t0009g0194a0001c0001t0009g0195a0001c0001t0009g0196others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.858-59T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615885 | ||||||
chr14:56615930
|
A | G | 195 | a0001c0001t0001g0121a0001c0001t0001g0228a0001c0001t0001g0276others(192): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.858-14A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615930 | ||||||
chr14:56616073
|
A | G | 1 | a0002c0006t0003g0287 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.941+46A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616073 | ||||||
chr14:56616174
|
T | C | 5 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(2): Show | 5 | NA18939.hp1 NA18964.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.941+147T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616174 | ||||||
chr14:56616207
|
A | G | 1 | a0003c0007t0001g0253 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.941+180A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616207 | ||||||
chr14:56616219
|
A | C | 17 | a0001c0001t0001g0276a0001c0001t0001g0277a0002c0005t0001g0011others(14): Show | 19 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.941+192A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616219 | ||||||
chr14:56616252
|
C | A | 1 | a0010c0016t0001g0092 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.941+225C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616252 | ||||||
chr14:56616262
|
C | G | 1 | a0001c0004t0003g0297 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.941+235C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616262 | ||||||
chr14:56616408
|
A | G | 2 | a0001c0001t0002g0238a0002c0005t0002g0014 | 3 | HG00642.hp1 HG00738.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.941+381A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616408 | ||||||
chr14:56616644
|
A | G | 1 | a0001c0004t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.942-539A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616644 | ||||||
chr14:56616893
|
C | T | 3 | a0002c0005t0012g0131a0002c0005t0012g0132a0002c0005t0012g0133 | 3 | HG03017.hp1 HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.942-290C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616893 | ||||||
chr14:56617021
|
T | A | 3 | a0004c0008t0004g0128a0004c0008t0004g0129a0004c0008t0004g0178 | 3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.942-162T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56617021 | ||||||
chr14:56617110
|
T | C | 7 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(4): Show | 7 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.942-73T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56617110 | ||||||
chr14:56617179
|
G | A | 91 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(88): Show | 95 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(92): Show |
splice_region_variant&intron_variant | LOW | c.942-4G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56617179 | ||||||
chr14:56617490
|
T | TTTAA | 224 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(221): Show | 239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.1056+194_1056+197d others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 56617490 | |||||
chr14:56617649
|
C | G | 1 | a0004c0008t0018g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1056+352C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56617649 | ||||||
chr14:56617695
|
G | T | 1 | a0002c0003t0001g0081 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1056+398G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56617695 | ||||||
chr14:56617718
|
A | G | 3 | a0004c0008t0004g0128a0004c0008t0004g0129a0004c0008t0004g0178 | 3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1056+421A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56617718 | ||||||
chr14:56617855
|
C | T | 3 | a0004c0008t0004g0128a0004c0008t0004g0129a0004c0008t0004g0178 | 3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1056+558C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56617855 | ||||||
chr14:56618099
|
A | G | 7 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(4): Show | 7 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1057-495A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56618099 | ||||||
chr14:56618304
|
C | G | 2 | a0001c0004t0003g0281a0001c0004t0003g0301 | 2 | NA18984.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1057-290C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56618304 | ||||||
chr14:56618343
|
A | G | 8 | a0001c0004t0004g0005a0001c0004t0004g0185a0001c0004t0004g0186others(5): Show | 10 | HG01081.hp2 HG01243.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1057-251A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56618343 | ||||||
chr14:56618420
|
A | C | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1057-174A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56618420 | ||||||
chr14:56618511
|
A | G | 1 | a0001c0001t0002g0226 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1057-83A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56618511 | ||||||
chr14:56618870
|
A | G | 3 | a0002c0005t0012g0131a0002c0005t0012g0132a0002c0005t0012g0133 | 3 | HG03017.hp1 HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1226+107A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56618870 | ||||||
chr14:56618939
|
A | G | 54 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(51): Show | 57 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.1226+176A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56618939 | ||||||
chr14:56619039
|
G | C | 33 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0028others(30): Show | 39 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1226+276G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56619039 | ||||||
chr14:56619071
|
A | G | 15 | a0002c0005t0001g0011a0002c0005t0001g0012a0002c0005t0001g0168others(12): Show | 17 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1226+308A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56619071 | ||||||
chr14:56619654
|
ATGGAAGA others(8): Show |
A | 2 | a0005c0009t0001g0164a0005c0009t0001g0169 | 2 | HG01109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1226+897_1226+911d others(17): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr14 | 56619654 | |||||
chr14:56619693
|
G | C | 1 | a0001c0001t0002g0238 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1226+930G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56619693 | ||||||
chr14:56619721
|
T | G | 6 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0205others(3): Show | 6 | HG00408.hp1 NA18945.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1226+958T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56619721 | ||||||
chr14:56619727
|
T | G | 1 | a0001c0001t0002g0200 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1226+964T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56619727 | ||||||
chr14:56619946
|
A | T | 11 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(8): Show | 11 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1226+1183A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56619946 | ||||||
chr14:56620062
|
C | G | 1 | a0002c0003t0001g0099 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1226+1299C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620062 | ||||||
chr14:56620240
|
C | T | 1 | a0001c0004t0003g0307 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1227-1291C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620240 | ||||||
chr14:56620287
|
T | C | 1 | a0001c0001t0005g0326 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1227-1244T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620287 | ||||||
chr14:56620300
|
A | T | 1 | a0003c0007t0001g0263 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1227-1231A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620300 | ||||||
chr14:56620361
|
C | T | 1 | a0004c0008t0018g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1227-1170C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620361 | ||||||
chr14:56620400
|
A | G | 85 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(82): Show | 88 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.1227-1131A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620400 | ||||||
chr14:56620414
|
C | A | 2 | a0001c0001t0001g0121a0007c0012t0001g0120 | 2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1227-1117C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620414 | ||||||
chr14:56620428
|
C | A | 104 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(101): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1227-1103C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620428 | ||||||
chr14:56620588
|
G | A | 4 | a0001c0001t0008g0124a0001c0001t0008g0125a0001c0001t0008g0126others(1): Show | 4 | HG02523.hp1 NA18943.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227-943G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620588 | ||||||
chr14:56620703
|
G | A | 4 | a0001c0001t0008g0124a0001c0001t0008g0125a0001c0001t0008g0126others(1): Show | 4 | HG02523.hp1 NA18943.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227-828G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620703 | ||||||
chr14:56620808
|
T | A | 1 | a0010c0016t0001g0092 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1227-723T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620808 | ||||||
chr14:56621153
|
G | A | 1 | a0001c0002t0001g0078 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1227-378G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56621153 | ||||||
chr14:56621161
|
G | GCAA | 40 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(37): Show | 41 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1227-370_1227-369i others(5): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56621161 | ||||||
chr14:56621168
|
T | C | 3 | a0004c0008t0004g0128a0004c0008t0004g0129a0004c0008t0004g0178 | 3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1227-363T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56621168 | ||||||
chr14:56621252
|
GA | G | 14 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(11): Show | 16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1227-273delA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr14 | 56621252 | |||||
chr14:56621275
|
A | G | 2 | a0001c0001t0001g0121a0007c0012t0001g0120 | 2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1227-256A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56621275 | ||||||
chr14:56621330
|
A | AT | 54 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(51): Show | 57 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.1227-193dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr14 | 56621330 | |||||
chr14:56621352
|
A | T | 205 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(202): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1227-179A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56621352 | ||||||
chr14:56621363
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1227-168A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56621363 | ||||||
chr14:56621451
|
T | A | 1 | a0004c0008t0018g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1227-80T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56621451 | ||||||
chr14:56621715
|
A | T | 54 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(51): Show | 57 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.1398+13A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56621715 | ||||||
chr14:56621788
|
C | T | 78 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(75): Show | 81 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.1398+86C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56621788 | ||||||
chr14:56622180
|
A | G | 6 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(3): Show | 6 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1398+478A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622180 | ||||||
chr14:56622297
|
C | T | 3 | a0004c0008t0004g0128a0004c0008t0004g0129a0004c0008t0004g0178 | 3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1398+595C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622297 | ||||||
chr14:56622341
|
T | A | 38 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0297others(35): Show | 39 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1398+639T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622341 | ||||||
chr14:56622342
|
C | A | 40 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(37): Show | 41 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1398+640C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622342 | ||||||
chr14:56622342
|
C | CA | 185 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(182): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1398+663dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr14 | 56622342 | |||||
chr14:56622342
|
C | CAA | 39 | a0001c0001t0001g0142a0001c0001t0001g0162a0001c0001t0002g0207others(36): Show | 39 | HG00438.hp1 HG00621.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.1398+662_1398+663d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr14 | 56622342 | |||||
chr14:56622381
|
C | T | 54 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(51): Show | 57 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.1398+679C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622381 | ||||||
chr14:56622521
|
G | C | 7 | a0002c0003t0001g0038a0002c0003t0001g0057a0002c0003t0001g0059others(4): Show | 7 | HG00423.hp2 HG02074.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+819G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622521 | ||||||
chr14:56622699
|
G | A | 1 | a0002c0005t0001g0275 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1398+997G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622699 | ||||||
chr14:56622752
|
A | G | 1 | a0002c0003t0001g0031 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1398+1050A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622752 | ||||||
chr14:56622821
|
G | A | 1 | a0002c0005t0001g0168 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1398+1119G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622821 | ||||||
chr14:56622827
|
T | G | 1 | a0010c0016t0001g0092 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1398+1125T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622827 | ||||||
chr14:56622879
|
T | G | 216 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(213): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1398+1177T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622879 | ||||||
chr14:56622894
|
C | G | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1398+1192C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622894 | ||||||
chr14:56623191
|
T | C | 55 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(52): Show | 58 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.1398+1489T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623191 | ||||||
chr14:56623308
|
C | T | 1 | a0010c0016t0001g0092 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1398+1606C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623308 | ||||||
chr14:56623446
|
A | G | 1 | a0001c0002t0001g0076 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1398+1744A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623446 | ||||||
chr14:56623446
|
A | T | 1 | a0002c0003t0001g0098 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1398+1744A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623446 | ||||||
chr14:56623675
|
A | G | 1 | a0002c0003t0001g0049 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1399-1707A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623675 | ||||||
chr14:56623682
|
A | G | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02027.hp2 HG02040.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1399-1700A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623682 | ||||||
chr14:56623826
|
T | C | 1 | a0002c0005t0013g0211 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1399-1556T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623826 | ||||||
chr14:56623836
|
C | T | 1 | a0002c0005t0012g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1399-1546C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623836 | ||||||
chr14:56623870
|
A | G | 136 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0005g0324others(133): Show | 149 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.1399-1512A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623870 | ||||||
chr14:56623882
|
C | T | 2 | a0001c0001t0002g0220a0001c0001t0002g0225 | 2 | HG01175.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1399-1500C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623882 | ||||||
chr14:56624109
|
G | A | 1 | a0001c0001t0009g0199 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1399-1273G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624109 | ||||||
chr14:56624193
|
C | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0155 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1399-1189C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624193 | ||||||
chr14:56624205
|
A | G | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1399-1177A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624205 | ||||||
chr14:56624224
|
A | G | 3 | a0004c0008t0004g0128a0004c0008t0004g0129a0004c0008t0004g0178 | 3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1399-1158A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624224 | ||||||
chr14:56624349
|
G | A | 1 | a0001c0004t0004g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1399-1033G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624349 | ||||||
chr14:56624403
|
G | A | 1 | a0002c0003t0001g0050 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1399-979G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624403 | ||||||
chr14:56624410
|
T | C | 315 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(312): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.1399-972T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624410 | ||||||
chr14:56624428
|
T | G | 315 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(312): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.1399-954T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624428 | ||||||
chr14:56624431
|
T | G | 315 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(312): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.1399-951T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624431 | ||||||
chr14:56624441
|
T | G | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1399-941T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624441 | ||||||
chr14:56624452
|
C | A | 1 | a0001c0001t0008g0323 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1399-930C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624452 | ||||||
chr14:56624602
|
C | T | 2 | a0001c0002t0001g0046a0001c0002t0001g0102 | 2 | NA18982.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1399-780C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624602 | ||||||
chr14:56624646
|
A | G | 7 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(4): Show | 7 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1399-736A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624646 | ||||||
chr14:56624665
|
C | T | 2 | a0001c0001t0002g0122a0001c0001t0002g0123 | 2 | NA18945.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1399-717C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624665 | ||||||
chr14:56624671
|
G | A | 1 | a0001c0001t0005g0333 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1399-711G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624671 | ||||||
chr14:56624757
|
C | T | 1 | a0002c0005t0012g0133 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1399-625C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624757 | ||||||
chr14:56624840
|
G | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1399-542G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624840 | ||||||
chr14:56624844
|
G | A | 1 | a0003c0007t0022g0260 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1399-538G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624844 | ||||||
chr14:56624971
|
A | G | 3 | a0001c0001t0002g0202a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | NA18942.hp1 NA18969.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1399-411A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624971 | ||||||
chr14:56625002
|
A | G | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1399-380A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56625002 | ||||||
chr14:56625147
|
G | A | 2 | a0001c0001t0001g0121a0007c0012t0001g0120 | 2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1399-235G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56625147 | ||||||
chr14:56625313
|
A | T | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1399-69A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56625313 | ||||||
chr14:56625320
|
A | G | 119 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0002t0001g0001others(116): Show | 132 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1399-62A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56625320 | ||||||
chr14:56625721
|
T | G | 119 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0002t0001g0001others(116): Show | 132 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1547+191T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56625721 | ||||||
chr14:56625867
|
C | T | 1 | a0001c0001t0002g0207 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1547+337C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56625867 | ||||||
chr14:56626045
|
A | C | 115 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(112): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1547+515A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626045 | ||||||
chr14:56626069
|
C | A | 14 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(11): Show | 16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1547+539C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626069 | ||||||
chr14:56626090
|
C | T | 1 | a0001c0002t0001g0037 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1547+560C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626090 | ||||||
chr14:56626182
|
A | C | 56 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0122others(53): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1547+652A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626182 | ||||||
chr14:56626221
|
C | G | 3 | a0004c0008t0004g0128a0004c0008t0004g0129a0004c0008t0004g0178 | 3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1547+691C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626221 | ||||||
chr14:56626288
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1547+758C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626288 | ||||||
chr14:56626403
|
T | C | 1 | a0001c0002t0001g0096 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1547+873T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626403 | ||||||
chr14:56626435
|
A | G | 217 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(214): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1547+905A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626435 | ||||||
chr14:56626614
|
A | G | 1 | a0003c0007t0022g0260 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1547+1084A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626614 | ||||||
chr14:56626779
|
C | T | 56 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0122others(53): Show | 61 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1547+1249C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626779 | ||||||
chr14:56626827
|
G | A | 1 | a0001c0001t0008g0321 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1547+1297G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626827 | ||||||
chr14:56626914
|
T | C | 14 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1547+1384T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626914 | ||||||
chr14:56626916
|
A | G | 14 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(11): Show | 16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1547+1386A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626916 | ||||||
chr14:56626966
|
A | G | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1547+1436A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626966 | ||||||
chr14:56627086
|
A | G | 4 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0204others(1): Show | 5 | NA18947.hp1 NA18952.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1547+1556A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627086 | ||||||
chr14:56627167
|
AAT | A | 14 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(11): Show | 16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1547+1638_1547+163 others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627167 | ||||||
chr14:56627394
|
C | G | 1 | a0001c0001t0002g0207 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1547+1864C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627394 | ||||||
chr14:56627427
|
T | C | 1 | a0001c0002t0001g0104 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1547+1897T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627427 | ||||||
chr14:56627505
|
C | T | 1 | a0001c0001t0006g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1547+1975C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627505 | ||||||
chr14:56627653
|
AT | A | 4 | a0002c0003t0001g0050a0004c0008t0004g0128a0004c0008t0004g0129others(1): Show | 4 | HG01256.hp1 HG03195.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1547+2128delT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56627653 | |||||
chr14:56627658
|
T | C | 140 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(137): Show | 154 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1547+2128T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627658 | ||||||
chr14:56627658
|
TC | T | 32 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(29): Show | 34 | HG00621.hp1 HG01358.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1547+2135delC | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56627658 | |||||
chr14:56627664
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1547+2134C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627664 | ||||||
chr14:56627669
|
G | C | 4 | a0001c0001t0006g0245a0001c0001t0006g0246a0001c0001t0006g0247others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547+2139G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627669 | ||||||
chr14:56627704
|
G | A | 1 | a0001c0011t0001g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1547+2174G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627704 | ||||||
chr14:56627823
|
T | A | 1 | a0001c0001t0008g0321 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1547+2293T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627823 | ||||||
chr14:56627846
|
A | G | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1547+2316A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627846 | ||||||
chr14:56627900
|
G | A | 1 | a0002c0003t0001g0049 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1547+2370G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627900 | ||||||
chr14:56628204
|
G | T | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1547+2674G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628204 | ||||||
chr14:56628354
|
C | T | 1 | a0001c0001t0006g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1547+2824C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628354 | ||||||
chr14:56628411
|
G | A | 19 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(16): Show | 19 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.1547+2881G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628411 | ||||||
chr14:56628422
|
A | G | 56 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0122others(53): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1547+2892A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628422 | ||||||
chr14:56628511
|
A | G | 1 | a0001c0002t0019g0029 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1547+2981A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628511 | ||||||
chr14:56628520
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1547+2990A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628520 | ||||||
chr14:56628634
|
A | G | 14 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(11): Show | 16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1547+3104A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628634 | ||||||
chr14:56628694
|
T | A | 56 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0122others(53): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1547+3164T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628694 | ||||||
chr14:56628809
|
C | A | 19 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(16): Show | 19 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.1547+3279C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628809 | ||||||
chr14:56628896
|
CT | C | 142 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(139): Show | 156 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.1547+3378delT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56628896 | |||||
chr14:56628940
|
G | A | 1 | a0004c0008t0018g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1547+3410G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628940 | ||||||
chr14:56629029
|
G | T | 1 | a0001c0001t0001g0134 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1547+3499G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629029 | ||||||
chr14:56629271
|
G | GT | 116 | a0001c0001t0001g0121a0001c0001t0001g0166a0001c0001t0001g0167others(113): Show | 123 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1548-3709dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56629271 | |||||
chr14:56629271
|
G | GTT | 23 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0216others(20): Show | 25 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1548-3710_1548-370 others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56629271 | |||||
chr14:56629273
|
T | TG | 3 | a0002c0005t0002g0150a0002c0005t0002g0151a0002c0005t0002g0160 | 3 | HG02698.hp2 HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1548-3722_1548-372 others(5): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629273 | ||||||
chr14:56629377
|
A | T | 1 | a0002c0006t0003g0284 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1548-3618A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629377 | ||||||
chr14:56629628
|
G | A | 54 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(51): Show | 57 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.1548-3367G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629628 | ||||||
chr14:56629680
|
G | T | 291 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(288): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1548-3315G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629680 | ||||||
chr14:56629774
|
A | G | 1 | a0004c0008t0018g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1548-3221A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629774 | ||||||
chr14:56629843
|
T | G | 1 | a0001c0001t0009g0199 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1548-3152T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629843 | ||||||
chr14:56629859
|
ACC | A | 11 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(8): Show | 11 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1548-3134_1548-313 others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56629859 | |||||
chr14:56629867
|
G | A | 1 | a0002c0003t0020g0090 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1548-3128G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629867 | ||||||
chr14:56629902
|
G | C | 6 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(3): Show | 6 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1548-3093G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629902 | ||||||
chr14:56629939
|
G | C | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1548-3056G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629939 | ||||||
chr14:56630021
|
A | G | 2 | a0001c0004t0003g0298a0001c0004t0003g0307 | 2 | HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1548-2974A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630021 | ||||||
chr14:56630042
|
G | GA | 34 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(31): Show | 36 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1548-2942dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56630042 | |||||
chr14:56630042
|
G | GAA | 40 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(37): Show | 41 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1548-2943_1548-294 others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56630042 | |||||
chr14:56630259
|
T | G | 307 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(304): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.1548-2736T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630259 | ||||||
chr14:56630314
|
A | G | 2 | a0001c0001t0002g0202a0001c0001t0002g0215 | 2 | NA18942.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1548-2681A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630314 | ||||||
chr14:56630384
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1548-2611A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630384 | ||||||
chr14:56630421
|
T | G | 1 | a0001c0004t0004g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1548-2574T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630421 | ||||||
chr14:56630423
|
A | G | 4 | a0001c0001t0008g0124a0001c0001t0008g0125a0001c0001t0008g0126others(1): Show | 4 | HG02523.hp1 NA18943.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1548-2572A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630423 | ||||||
chr14:56630466
|
T | C | 1 | a0001c0004t0004g0186 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1548-2529T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630466 | ||||||
chr14:56630472
|
C | CT | 16 | a0001c0001t0001g0276a0001c0001t0001g0277a0002c0005t0001g0011others(13): Show | 18 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1548-2514dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56630472 | |||||
chr14:56630573
|
C | T | 1 | a0003c0007t0001g0265 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1548-2422C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630573 | ||||||
chr14:56630577
|
A | G | 1 | a0002c0006t0003g0317 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1548-2418A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630577 | ||||||
chr14:56630688
|
C | T | 10 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(7): Show | 10 | HG00639.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1548-2307C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630688 | ||||||
chr14:56630904
|
C | T | 3 | a0002c0005t0001g0175a0002c0005t0001g0176a0002c0005t0001g0233 | 3 | HG02257.hp1 HG02895.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1548-2091C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630904 | ||||||
chr14:56630905
|
G | A | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1548-2090G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630905 | ||||||
chr14:56630972
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1548-2023G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630972 | ||||||
chr14:56630975
|
G | A | 14 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(11): Show | 16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1548-2020G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630975 | ||||||
chr14:56630982
|
T | A | 15 | a0002c0005t0001g0011a0002c0005t0001g0012a0002c0005t0001g0168others(12): Show | 17 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1548-2013T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630982 | ||||||
chr14:56631024
|
A | G | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1548-1971A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631024 | ||||||
chr14:56631118
|
A | ACAAGCTC others(1): Show |
15 | a0002c0005t0001g0011a0002c0005t0001g0012a0002c0005t0001g0168others(12): Show | 17 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1548-1877_1548-187 others(12): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631118 | ||||||
chr14:56631177
|
C | T | 14 | a0002c0005t0001g0011a0002c0005t0001g0012a0002c0005t0001g0168others(11): Show | 16 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1548-1818C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631177 | ||||||
chr14:56631226
|
C | T | 15 | a0002c0005t0001g0011a0002c0005t0001g0012a0002c0005t0001g0168others(12): Show | 17 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1548-1769C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631226 | ||||||
chr14:56631262
|
C | T | 1 | a0004c0008t0018g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1548-1733C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631262 | ||||||
chr14:56631361
|
G | A | 51 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0122others(48): Show | 57 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.1548-1634G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631361 | ||||||
chr14:56631400
|
ATCACCTG others(3): Show |
A | 1 | a0006c0019t0001g0045 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1548-1591_1548-158 others(14): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56631400 | |||||
chr14:56631491
|
T | C | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1548-1504T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631491 | ||||||
chr14:56631516
|
C | T | 1 | a0001c0001t0008g0125 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1548-1479C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631516 | ||||||
chr14:56631622
|
C | CA | 177 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(174): Show | 193 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.1548-1357dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56631622 | |||||
chr14:56631629
|
A | AAC | 110 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(107): Show | 119 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1548-1365_1548-136 others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56631629 | |||||
chr14:56631642
|
A | G | 7 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(4): Show | 7 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1548-1353A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631642 | ||||||
chr14:56631700
|
G | C | 1 | a0001c0004t0003g0298 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1548-1295G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631700 | ||||||
chr14:56631748
|
T | C | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(25): Show | 31 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1548-1247T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631748 | ||||||
chr14:56631815
|
A | G | 1 | a0002c0005t0012g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1548-1180A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631815 | ||||||
chr14:56631839
|
G | A | 135 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(132): Show | 148 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1548-1156G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631839 | ||||||
chr14:56631867
|
T | A | 309 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(306): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1548-1128T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631867 | ||||||
chr14:56631872
|
G | A | 2 | a0001c0004t0004g0182a0001c0004t0004g0183 | 2 | HG01243.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1548-1123G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631872 | ||||||
chr14:56631961
|
C | T | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 28 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.1548-1034C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631961 | ||||||
chr14:56632158
|
C | T | 7 | a0002c0003t0001g0038a0002c0003t0001g0057a0002c0003t0001g0059others(4): Show | 7 | HG00423.hp2 HG02074.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.1548-837C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56632158 | ||||||
chr14:56632167
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1548-828G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56632167 | ||||||
chr14:56632185
|
T | G | 18 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1548-810T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56632185 | ||||||
chr14:56632248
|
C | T | 3 | a0004c0008t0004g0128a0004c0008t0004g0129a0004c0008t0004g0178 | 3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1548-747C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56632248 | ||||||
chr14:56632417
|
A | G | 1 | a0003c0007t0001g0250 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1548-578A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56632417 | ||||||
chr14:56632462
|
C | T | 1 | a0010c0016t0001g0092 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1548-533C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56632462 | ||||||
chr14:56632574
|
C | CT | 119 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0002t0001g0001others(116): Show | 132 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1548-414dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56632574 | |||||
chr14:56632619
|
C | CT | 6 | a0001c0002t0001g0021a0001c0002t0001g0033a0001c0002t0001g0070others(3): Show | 6 | NA18939.hp2 NA18959.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.1548-370dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56632619 | |||||
chr14:56632792
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1548-203G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56632792 | ||||||
chr14:56633234
|
T | G | 7 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(4): Show | 7 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1724+63T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633234 | ||||||
chr14:56633235
|
A | G | 1 | a0001c0001t0005g0333 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1724+64A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633235 | ||||||
chr14:56633258
|
A | ATT | 20 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(17): Show | 20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1724+97_1724+98dup others(2): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 56633258 | |||||
chr14:56633258
|
AT | A | 33 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(30): Show | 33 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1724+98delT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 56633258 | |||||
chr14:56633258
|
ATTTT | A | 7 | a0001c0004t0011g0310a0001c0004t0011g0311a0001c0004t0011g0312others(4): Show | 8 | HG01433.hp1 HG02559.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1724+95_1724+98del others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 56633258 | |||||
chr14:56633292
|
T | G | 1 | a0009c0017t0007g0019 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1724+121T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633292 | ||||||
chr14:56633434
|
T | G | 1 | a0001c0001t0002g0123 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1724+263T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633434 | ||||||
chr14:56633550
|
T | A | 1 | a0001c0011t0001g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1724+379T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633550 | ||||||
chr14:56633607
|
T | C | 42 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(39): Show | 42 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.1724+436T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633607 | ||||||
chr14:56633612
|
G | A | 1 | a0002c0003t0001g0057 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1724+441G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633612 | ||||||
chr14:56633614
|
G | A | 20 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(17): Show | 20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1724+443G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633614 | ||||||
chr14:56633731
|
A | T | 20 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(17): Show | 20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1724+560A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633731 | ||||||
chr14:56633794
|
T | TCA | 20 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(17): Show | 20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1724+636_1724+637d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 56633794 | |||||
chr14:56633808
|
A | G | 7 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(4): Show | 7 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1724+637A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633808 | ||||||
chr14:56633874
|
A | G | 1 | a0003c0007t0001g0257 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1724+703A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633874 | ||||||
chr14:56634333
|
A | G | 5 | a0001c0002t0001g0002a0001c0002t0001g0039a0001c0002t0001g0066others(2): Show | 9 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1725-566A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634333 | ||||||
chr14:56634334
|
G | T | 37 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(34): Show | 39 | HG00621.hp1 HG01081.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1725-565G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634334 | ||||||
chr14:56634408
|
A | C | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1725-491A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634408 | ||||||
chr14:56634516
|
A | T | 1 | a0002c0003t0001g0064 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1725-383A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634516 | ||||||
chr14:56634534
|
C | T | 189 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(186): Show | 200 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1725-365C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634534 | ||||||
chr14:56634535
|
C | G | 312 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(309): Show | 336 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(333): Show |
intron_variant | MODIFIER | c.1725-364C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634535 | ||||||
chr14:56634679
|
G | T | 287 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(284): Show | 309 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.1725-220G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634679 | ||||||
chr14:56634694
|
G | T | 295 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(292): Show | 317 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.1725-205G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634694 | ||||||
chr14:56634709
|
G | A | 1 | a0001c0001t0002g0212 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1725-190G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634709 | ||||||
chr14:56634842
|
C | CA | 11 | a0002c0005t0001g0011a0002c0005t0001g0012a0002c0005t0001g0170others(8): Show | 13 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1725-42dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 56634842 | |||||
chr14:56634964
|
A | G | 219 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(216): Show | 239 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1778+12A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56634964 | ||||||
chr14:56635288
|
C | T | 1 | a0002c0005t0012g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1778+336C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56635288 | ||||||
chr14:56635447
|
T | C | 1 | a0001c0001t0009g0199 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1778+495T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56635447 | ||||||
chr14:56635469
|
T | TGTTAAAG others(9): Show |
7 | a0001c0004t0011g0310a0001c0004t0011g0311a0001c0004t0011g0312others(4): Show | 8 | HG01433.hp1 HG02559.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1778+518_1778+533d others(18): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr14 | 56635469 | |||||
chr14:56635738
|
C | T | 20 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(17): Show | 20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1779-770C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56635738 | ||||||
chr14:56635771
|
T | C | 14 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(11): Show | 16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1779-737T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56635771 | ||||||
chr14:56635775
|
G | A | 1 | a0001c0002t0001g0034 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1779-733G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56635775 | ||||||
chr14:56635816
|
G | A | 24 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(21): Show | 27 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.1779-692G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56635816 | ||||||
chr14:56635844
|
A | AAT | 63 | a0001c0001t0001g0163a0001c0001t0002g0006a0001c0001t0002g0122others(60): Show | 69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.1779-650_1779-649d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr14 | 56635844 | |||||
chr14:56635844
|
AAT | A | 44 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(41): Show | 47 | HG00621.hp1 HG01081.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1779-650_1779-649d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr14 | 56635844 | |||||
chr14:56635980
|
G | GCATAATT others(16): Show |
5 | a0002c0006t0003g0284a0002c0006t0003g0291a0002c0006t0003g0292others(2): Show | 5 | NA18979.hp2 NA19002.hp1 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.1779-527_1779-505d others(25): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr14 | 56635980 | |||||
chr14:56636012
|
G | A | 1 | a0001c0001t0006g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1779-496G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56636012 | ||||||
chr14:56636158
|
G | A | 4 | a0001c0001t0005g0325a0001c0001t0005g0326a0001c0001t0005g0327others(1): Show | 4 | NA18959.hp1 NA18967.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.1779-350G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56636158 | ||||||
chr14:56636225
|
T | TAACAATA others(6): Show |
7 | a0001c0004t0011g0310a0001c0004t0011g0311a0001c0004t0011g0312others(4): Show | 8 | HG01433.hp1 HG02559.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1779-281_1779-269d others(15): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr14 | 56636225 | |||||
chr14:56636504
|
C | G | 11 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(8): Show | 11 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.1779-4C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56636504 | ||||||
chr14:56636661
|
A | G | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+63A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56636661 | ||||||
chr14:56636663
|
A | G | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+65A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56636663 | ||||||
chr14:56636780
|
G | A | 4 | a0002c0005t0013g0211a0003c0007t0013g0259a0003c0007t0013g0262others(1): Show | 4 | HG03831.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1869+182G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56636780 | ||||||
chr14:56636794
|
GAAT | G | 7 | a0001c0004t0011g0310a0001c0004t0011g0311a0001c0004t0011g0312others(4): Show | 8 | HG01433.hp1 HG02559.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1869+201_1869+203d others(5): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56636794 | |||||
chr14:56637007
|
C | T | 25 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(22): Show | 25 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1869+409C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637007 | ||||||
chr14:56637044
|
G | A | 5 | a0001c0004t0011g0310a0001c0004t0011g0311a0001c0004t0011g0312others(2): Show | 5 | HG01433.hp1 HG02559.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1869+446G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637044 | ||||||
chr14:56637068
|
T | C | 1 | a0001c0002t0001g0109 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1869+470T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637068 | ||||||
chr14:56637230
|
T | C | 1 | a0001c0011t0001g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1869+632T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637230 | ||||||
chr14:56637268
|
C | T | 296 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(293): Show | 318 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.1869+670C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637268 | ||||||
chr14:56637321
|
G | C | 2 | a0001c0002t0001g0109a0002c0003t0001g0110 | 2 | NA19010.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1869+723G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637321 | ||||||
chr14:56637392
|
A | C | 4 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0223others(1): Show | 4 | HG01993.hp1 HG02148.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1869+794A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637392 | ||||||
chr14:56637409
|
G | A | 20 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(17): Show | 20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1869+811G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637409 | ||||||
chr14:56637423
|
C | T | 106 | a0001c0001t0001g0149a0001c0001t0001g0228a0001c0002t0001g0001others(103): Show | 117 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1869+825C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637423 | ||||||
chr14:56637435
|
T | C | 1 | a0004c0008t0004g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1869+837T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637435 | ||||||
chr14:56637522
|
A | G | 8 | a0002c0005t0001g0011a0002c0005t0001g0012a0002c0005t0001g0170others(5): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1869+924A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637522 | ||||||
chr14:56637714
|
G | A | 1 | a0002c0006t0003g0282 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1869+1116G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637714 | ||||||
chr14:56637853
|
T | TCCCTGCT others(13): Show |
20 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(17): Show | 20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1869+1269_1869+127 others(24): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56637853 | |||||
chr14:56637877
|
G | C | 3 | a0004c0008t0004g0128a0004c0008t0004g0129a0004c0008t0004g0178 | 3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1869+1279G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637877 | ||||||
chr14:56637923
|
TTGTGAGT others(2): Show |
T | 4 | a0001c0001t0005g0325a0001c0001t0005g0326a0001c0001t0005g0327others(1): Show | 4 | NA18959.hp1 NA18967.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.1869+1332_1869+134 others(13): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56637923 | |||||
chr14:56637948
|
AG | A | 3 | a0004c0008t0004g0128a0004c0008t0004g0129a0004c0008t0004g0178 | 3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1869+1353delG | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56637948 | |||||
chr14:56638073
|
G | GCTAACCA others(21): Show |
33 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(30): Show | 33 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1869+1476_1869+150 others(32): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56638073 | |||||
chr14:56638133
|
A | G | 253 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(250): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1869+1535A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638133 | ||||||
chr14:56638191
|
A | G | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+1593A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638191 | ||||||
chr14:56638257
|
C | A | 1 | a0004c0008t0018g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1869+1659C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638257 | ||||||
chr14:56638268
|
A | G | 5 | a0001c0001t0001g0276a0001c0001t0001g0277a0004c0008t0004g0128others(2): Show | 5 | HG02257.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1869+1670A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638268 | ||||||
chr14:56638476
|
C | T | 20 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(17): Show | 20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1869+1878C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638476 | ||||||
chr14:56638511
|
T | C | 6 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(3): Show | 6 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1869+1913T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638511 | ||||||
chr14:56638612
|
A | C | 111 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(108): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1869+2014A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638612 | ||||||
chr14:56638638
|
A | AATGAGGC others(45): Show |
1 | a0003c0007t0001g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1869+2041_1869+209 others(56): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56638638 | |||||
chr14:56638749
|
A | G | 1 | a0001c0004t0011g0311 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1869+2151A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638749 | ||||||
chr14:56638766
|
G | C | 1 | a0001c0001t0009g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1869+2168G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638766 | ||||||
chr14:56638793
|
AGCAGG | A | 4 | a0002c0005t0013g0211a0003c0007t0013g0259a0003c0007t0013g0262others(1): Show | 4 | HG03831.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1869+2203_1869+220 others(9): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56638793 | |||||
chr14:56638799
|
G | A | 4 | a0001c0001t0002g0202a0001c0001t0002g0215a0001c0001t0002g0216others(1): Show | 4 | NA18942.hp1 NA18969.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1869+2201G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638799 | ||||||
chr14:56638804
|
G | A | 1 | a0001c0004t0003g0297 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1869+2206G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638804 | ||||||
chr14:56638806
|
G | A | 20 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(17): Show | 20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1869+2208G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638806 | ||||||
chr14:56638826
|
A | G | 1 | a0001c0001t0006g0113 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1869+2228A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638826 | ||||||
chr14:56638918
|
A | T | 7 | a0001c0004t0011g0310a0001c0004t0011g0311a0001c0004t0011g0312others(4): Show | 8 | HG01433.hp1 HG02559.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1869+2320A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638918 | ||||||
chr14:56638925
|
A | G | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+2327A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638925 | ||||||
chr14:56638929
|
C | T | 5 | a0001c0004t0011g0310a0001c0004t0011g0311a0001c0004t0011g0312others(2): Show | 5 | HG01433.hp1 HG02559.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1869+2331C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638929 | ||||||
chr14:56638948
|
C | G | 1 | a0002c0003t0001g0050 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1869+2350C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638948 | ||||||
chr14:56639022
|
A | G | 6 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(3): Show | 6 | HG01358.hp1 HG02559.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1869+2424A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639022 | ||||||
chr14:56639192
|
A | G | 2 | a0004c0008t0004g0128a0004c0008t0004g0178 | 2 | HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1869+2594A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639192 | ||||||
chr14:56639234
|
ACAGGGTA others(12): Show |
A | 39 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(36): Show | 42 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1869+2656_1869+267 others(23): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56639234 | |||||
chr14:56639243
|
C | A | 1 | a0002c0003t0007g0036 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1869+2645C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639243 | ||||||
chr14:56639298
|
CTA | C | 13 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(10): Show | 15 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1869+2701_1869+270 others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639298 | ||||||
chr14:56639372
|
A | G | 1 | a0004c0008t0004g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1869+2774A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639372 | ||||||
chr14:56639574
|
C | T | 25 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(22): Show | 25 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1869+2976C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639574 | ||||||
chr14:56639583
|
C | T | 14 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(11): Show | 14 | HG00639.hp2 HG01109.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1869+2985C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639583 | ||||||
chr14:56639584
|
G | A | 1 | a0009c0017t0007g0019 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1869+2986G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639584 | ||||||
chr14:56639590
|
T | C | 1 | a0004c0008t0018g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1869+2992T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639590 | ||||||
chr14:56639704
|
C | T | 5 | a0001c0001t0006g0244a0001c0001t0006g0245a0001c0001t0006g0246others(2): Show | 5 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1869+3106C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639704 | ||||||
chr14:56639705
|
G | A | 1 | a0002c0005t0001g0275 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1869+3107G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639705 | ||||||
chr14:56639777
|
T | TCCCACCC others(16): Show |
1 | a0002c0006t0003g0292 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1869+3181_1869+320 others(27): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56639777 | |||||
chr14:56639784
|
C | T | 25 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(22): Show | 25 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1869+3186C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639784 | ||||||
chr14:56639839
|
C | G | 1 | a0001c0001t0009g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1869+3241C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639839 | ||||||
chr14:56639991
|
C | T | 1 | a0001c0001t0008g0322 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1869+3393C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639991 | ||||||
chr14:56640001
|
A | G | 25 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(22): Show | 25 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1869+3403A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640001 | ||||||
chr14:56640017
|
C | G | 2 | a0001c0001t0009g0194a0001c0001t0009g0197 | 2 | HG01891.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1869+3419C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640017 | ||||||
chr14:56640030
|
G | C | 11 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(8): Show | 11 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1869+3432G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640030 | ||||||
chr14:56640310
|
CA | C | 25 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(22): Show | 25 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1869+3714delA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56640310 | |||||
chr14:56640322
|
T | A | 25 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(22): Show | 25 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1869+3724T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640322 | ||||||
chr14:56640346
|
G | A | 1 | a0011c0015t0001g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1869+3748G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640346 | ||||||
chr14:56640640
|
C | T | 1 | a0002c0003t0007g0020 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1869+4042C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640640 | ||||||
chr14:56640657
|
G | A | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4059G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640657 | ||||||
chr14:56640673
|
G | C | 1 | a0001c0004t0003g0306 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1869+4075G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640673 | ||||||
chr14:56640689
|
C | T | 11 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(8): Show | 11 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1869+4091C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640689 | ||||||
chr14:56640796
|
C | T | 4 | a0002c0005t0013g0211a0003c0007t0013g0259a0003c0007t0013g0262others(1): Show | 4 | HG03831.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1869+4198C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640796 | ||||||
chr14:56640807
|
C | T | 1 | a0001c0011t0001g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1869+4209C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640807 | ||||||
chr14:56640818
|
GA | G | 34 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(31): Show | 34 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1869+4224delA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56640818 | |||||
chr14:56640832
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1869+4234G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640832 | ||||||
chr14:56640899
|
G | A | 1 | a0003c0007t0001g0250 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1869+4301G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640899 | ||||||
chr14:56640928
|
G | T | 1 | a0002c0005t0002g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1869+4330G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640928 | ||||||
chr14:56640956
|
GAAAC | G | 14 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(11): Show | 16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1869+4366_1869+436 others(8): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56640956 | |||||
chr14:56640975
|
A | C | 16 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(13): Show | 16 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.1869+4377A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640975 | ||||||
chr14:56640982
|
T | G | 3 | a0001c0002t0001g0047a0001c0002t0001g0052a0001c0002t0001g0104 | 3 | HG00741.hp2 HG01993.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1869+4384T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640982 | ||||||
chr14:56641032
|
T | C | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4434T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641032 | ||||||
chr14:56641058
|
C | T | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4460C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641058 | ||||||
chr14:56641059
|
A | G | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4461A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641059 | ||||||
chr14:56641060
|
G | C | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4462G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641060 | ||||||
chr14:56641062
|
A | G | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4464A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641062 | ||||||
chr14:56641069
|
G | C | 106 | a0001c0001t0001g0149a0001c0001t0001g0228a0001c0002t0001g0001others(103): Show | 117 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1869+4471G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641069 | ||||||
chr14:56641099
|
C | T | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4501C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641099 | ||||||
chr14:56641104
|
T | C | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4506T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641104 | ||||||
chr14:56641115
|
T | C | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4517T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641115 | ||||||
chr14:56641121
|
C | T | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4523C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641121 | ||||||
chr14:56641130
|
T | G | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4532T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641130 | ||||||
chr14:56641138
|
G | A | 97 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(94): Show | 100 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(97): Show |
intron_variant | MODIFIER | c.1869+4540G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641138 | ||||||
chr14:56641140
|
A | G | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4542A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641140 | ||||||
chr14:56641145
|
A | G | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4547A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641145 | ||||||
chr14:56641166
|
A | G | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4568A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641166 | ||||||
chr14:56641207
|
TGATTGTC others(1): Show |
T | 6 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(3): Show | 6 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1869+4614_1869+462 others(12): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56641207 | |||||
chr14:56641256
|
A | T | 4 | a0002c0005t0013g0211a0003c0007t0013g0259a0003c0007t0013g0262others(1): Show | 4 | HG03831.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1869+4658A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641256 | ||||||
chr14:56641454
|
C | T | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4856C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641454 | ||||||
chr14:56641518
|
C | T | 34 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(31): Show | 34 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1869+4920C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641518 | ||||||
chr14:56641650
|
A | G | 20 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(17): Show | 20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1869+5052A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641650 | ||||||
chr14:56641723
|
A | G | 1 | a0001c0002t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1869+5125A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641723 | ||||||
chr14:56641751
|
G | A | 1 | a0001c0001t0005g0324 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1869+5153G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641751 | ||||||
chr14:56641817
|
G | A | 1 | a0002c0003t0001g0084 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1869+5219G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641817 | ||||||
chr14:56641884
|
TTAAA | T | 14 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(11): Show | 16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1869+5287_1869+529 others(8): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641884 | ||||||
chr14:56641902
|
G | A | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+5304G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641902 | ||||||
chr14:56641909
|
CAAAG | C | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+5314_1869+531 others(8): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56641909 | |||||
chr14:56641986
|
A | T | 2 | a0003c0007t0001g0253a0003c0007t0001g0270 | 2 | HG00140.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1870-5257A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641986 | ||||||
chr14:56642112
|
T | C | 21 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(18): Show | 24 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1870-5131T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642112 | ||||||
chr14:56642125
|
C | A | 3 | a0004c0008t0004g0128a0004c0008t0004g0129a0004c0008t0004g0178 | 3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1870-5118C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642125 | ||||||
chr14:56642148
|
C | T | 96 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(93): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1870-5095C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642148 | ||||||
chr14:56642149
|
G | C | 14 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(11): Show | 16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1870-5094G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642149 | ||||||
chr14:56642153
|
C | T | 35 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(32): Show | 35 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.1870-5090C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642153 | ||||||
chr14:56642154
|
G | A | 8 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0222others(5): Show | 8 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1870-5089G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642154 | ||||||
chr14:56642188
|
A | C | 2 | a0002c0005t0001g0012a0002c0005t0001g0170 | 3 | HG01891.hp2 HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1870-5055A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642188 | ||||||
chr14:56642220
|
G | A | 297 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(294): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.1870-5023G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642220 | ||||||
chr14:56642265
|
A | C | 1 | a0001c0001t0005g0334 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1870-4978A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642265 | ||||||
chr14:56642292
|
A | G | 1 | a0001c0004t0003g0296 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1870-4951A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642292 | ||||||
chr14:56642296
|
A | G | 14 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(11): Show | 16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1870-4947A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642296 | ||||||
chr14:56642366
|
A | G | 14 | a0001c0001t0002g0232a0001c0001t0002g0234a0001c0001t0002g0235others(11): Show | 14 | HG01358.hp1 HG01891.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.1870-4877A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642366 | ||||||
chr14:56642460
|
C | A | 4 | a0002c0005t0013g0211a0003c0007t0013g0259a0003c0007t0013g0262others(1): Show | 4 | HG03831.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1870-4783C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642460 | ||||||
chr14:56642461
|
G | A | 6 | a0001c0004t0004g0179a0001c0004t0004g0180a0001c0004t0004g0181others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1870-4782G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642461 | ||||||
chr14:56642497
|
A | G | 1 | a0002c0003t0021g0042 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1870-4746A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642497 | ||||||
chr14:56642530
|
G | A | 1 | a0002c0003t0007g0112 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1870-4713G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642530 | ||||||
chr14:56642578
|
C | A | 1 | a0003c0007t0001g0016 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1870-4665C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642578 | ||||||
chr14:56642620
|
C | T | 1 | a0002c0005t0001g0275 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1870-4623C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642620 | ||||||
chr14:56642673
|
G | A | 1 | a0002c0003t0007g0112 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1870-4570G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642673 | ||||||
chr14:56642874
|
A | G | 4 | a0001c0001t0008g0124a0001c0001t0008g0125a0001c0001t0008g0126others(1): Show | 4 | HG02523.hp1 NA18943.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1870-4369A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642874 | ||||||
chr14:56642882
|
G | A | 1 | a0001c0002t0001g0062 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1870-4361G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642882 | ||||||
chr14:56642944
|
G | A | 14 | a0001c0002t0001g0034a0001c0002t0001g0044a0001c0002t0001g0051others(11): Show | 16 | HG00423.hp1 HG00673.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1870-4299G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642944 | ||||||
chr14:56642944
|
G | T | 1 | a0003c0007t0001g0252 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1870-4299G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642944 | ||||||
chr14:56643037
|
A | G | 5 | a0001c0001t0009g0194a0001c0001t0009g0195a0001c0001t0009g0196others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1870-4206A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643037 | ||||||
chr14:56643059
|
T | G | 1 | a0001c0002t0001g0034 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1870-4184T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643059 | ||||||
chr14:56643063
|
T | C | 1 | a0001c0002t0001g0109 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1870-4180T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643063 | ||||||
chr14:56643117
|
G | T | 10 | a0001c0001t0001g0121a0001c0001t0001g0149a0001c0004t0003g0281others(7): Show | 12 | HG02258.hp2 HG02486.hp1 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.1870-4126G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643117 | ||||||
chr14:56643199
|
A | G | 98 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(95): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1870-4044A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643199 | ||||||
chr14:56643250
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1870-3993A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643250 | ||||||
chr14:56643288
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1870-3955A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643288 | ||||||
chr14:56643358
|
C | T | 1 | a0001c0001t0002g0231 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1870-3885C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643358 | ||||||
chr14:56643415
|
A | G | 1 | a0002c0006t0003g0294 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1870-3828A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643415 | ||||||
chr14:56643418
|
A | C | 2 | a0001c0002t0001g0096a0001c0002t0001g0097 | 2 | NA19002.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1870-3825A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643418 | ||||||
chr14:56643484
|
A | C | 21 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(18): Show | 21 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.1870-3759A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643484 | ||||||
chr14:56643494
|
T | C | 1 | a0002c0005t0001g0275 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1870-3749T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643494 | ||||||
chr14:56643506
|
A | G | 1 | a0001c0002t0001g0033 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1870-3737A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643506 | ||||||
chr14:56643577
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1870-3666A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643577 | ||||||
chr14:56643582
|
C | G | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1870-3661C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643582 | ||||||
chr14:56643624
|
A | G | 1 | a0002c0005t0002g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1870-3619A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643624 | ||||||
chr14:56643693
|
T | C | 5 | a0001c0001t0009g0194a0001c0001t0009g0195a0001c0001t0009g0196others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1870-3550T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643693 | ||||||
chr14:56643735
|
T | C | 38 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(35): Show | 41 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1870-3508T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643735 | ||||||
chr14:56643800
|
A | G | 4 | a0002c0005t0012g0131a0002c0005t0012g0132a0002c0005t0012g0133others(1): Show | 4 | HG02970.hp2 HG03017.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1870-3443A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643800 | ||||||
chr14:56643906
|
A | G | 2 | a0005c0009t0001g0164a0005c0009t0001g0169 | 2 | HG01109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1870-3337A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643906 | ||||||
chr14:56643929
|
C | T | 2 | a0001c0001t0001g0121a0007c0012t0001g0120 | 2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1870-3314C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643929 | ||||||
chr14:56644020
|
T | A | 1 | a0002c0003t0021g0042 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1870-3223T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644020 | ||||||
chr14:56644075
|
T | G | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1870-3168T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644075 | ||||||
chr14:56644271
|
A | G | 1 | a0002c0003t0017g0318 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1870-2972A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644271 | ||||||
chr14:56644272
|
C | G | 1 | a0003c0007t0001g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1870-2971C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644272 | ||||||
chr14:56644286
|
A | G | 1 | a0001c0001t0002g0243 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1870-2957A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644286 | ||||||
chr14:56644369
|
T | G | 20 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(17): Show | 20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1870-2874T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644369 | ||||||
chr14:56644498
|
T | A | 11 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(8): Show | 11 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1870-2745T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644498 | ||||||
chr14:56644499
|
T | A | 11 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(8): Show | 11 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1870-2744T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644499 | ||||||
chr14:56644585
|
G | C | 191 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(188): Show | 203 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1870-2658G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644585 | ||||||
chr14:56644605
|
G | A | 31 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(28): Show | 31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1870-2638G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644605 | ||||||
chr14:56644668
|
T | A | 20 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(17): Show | 20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1870-2575T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644668 | ||||||
chr14:56644707
|
G | C | 33 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(30): Show | 33 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1870-2536G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644707 | ||||||
chr14:56644723
|
G | A | 1 | a0001c0001t0006g0245 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1870-2520G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644723 | ||||||
chr14:56644744
|
A | G | 2 | a0001c0001t0008g0126a0004c0008t0018g0119 | 2 | NA19081.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1870-2499A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644744 | ||||||
chr14:56644776
|
T | A | 1 | a0001c0002t0001g0088 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1870-2467T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644776 | ||||||
chr14:56645028
|
A | G | 12 | a0001c0004t0004g0005a0001c0004t0004g0179a0001c0004t0004g0180others(9): Show | 14 | HG01081.hp2 HG01243.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1870-2215A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645028 | ||||||
chr14:56645086
|
T | C | 123 | a0001c0001t0001g0149a0001c0001t0001g0228a0001c0001t0002g0232others(120): Show | 135 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1870-2157T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645086 | ||||||
chr14:56645167
|
T | C | 11 | a0001c0001t0006g0113a0001c0001t0006g0115a0001c0001t0006g0116others(8): Show | 11 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1870-2076T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645167 | ||||||
chr14:56645208
|
G | A | 2 | a0001c0011t0001g0320a0004c0008t0005g0268 | 2 | HG01943.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1870-2035G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645208 | ||||||
chr14:56645244
|
C | CA | 150 | a0001c0001t0001g0149a0001c0001t0001g0228a0001c0001t0006g0113others(147): Show | 161 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.1870-1997dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56645244 | |||||
chr14:56645257
|
A | T | 2 | a0001c0002t0001g0109a0002c0003t0001g0110 | 2 | NA19010.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1870-1986A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645257 | ||||||
chr14:56645360
|
G | A | 140 | a0001c0001t0001g0149a0001c0001t0001g0228a0001c0002t0001g0001others(137): Show | 151 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.1870-1883G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645360 | ||||||
chr14:56645387
|
G | A | 9 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(6): Show | 9 | HG00639.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1870-1856G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645387 | ||||||
chr14:56645452
|
A | G | 2 | a0001c0001t0002g0006a0015c0021t0002g0006 | 3 | NA18952.hp2 NA19004.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1870-1791A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645452 | ||||||
chr14:56645481
|
G | T | 312 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(309): Show | 336 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(333): Show |
intron_variant | MODIFIER | c.1870-1762G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645481 | ||||||
chr14:56645501
|
G | A | 5 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(2): Show | 5 | NA18939.hp1 NA18964.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1870-1742G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645501 | ||||||
chr14:56645502
|
G | C | 8 | a0001c0004t0004g0005a0001c0004t0004g0185a0001c0004t0004g0186others(5): Show | 10 | HG01081.hp2 HG01243.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1870-1741G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645502 | ||||||
chr14:56645504
|
T | G | 1 | a0002c0003t0007g0112 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1870-1739T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645504 | ||||||
chr14:56645505
|
A | T | 1 | a0002c0003t0007g0112 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1870-1738A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645505 | ||||||
chr14:56645505
|
AG | A | 122 | a0001c0001t0001g0149a0001c0001t0001g0228a0001c0002t0001g0001others(119): Show | 135 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1870-1732delG | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56645505 | |||||
chr14:56645506
|
G | A | 1 | a0002c0003t0007g0112 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1870-1737G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645506 | ||||||
chr14:56645517
|
T | C | 4 | a0002c0005t0012g0131a0002c0005t0012g0132a0002c0005t0012g0133others(1): Show | 4 | HG02970.hp2 HG03017.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1870-1726T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645517 | ||||||
chr14:56645567
|
A | G | 20 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(17): Show | 20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1870-1676A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645567 | ||||||
chr14:56645627
|
AAAACTT | A | 103 | a0001c0001t0001g0149a0001c0001t0001g0228a0001c0002t0001g0001others(100): Show | 114 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1870-1612_1870-160 others(10): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56645627 | |||||
chr14:56645634
|
A | C | 1 | a0001c0001t0001g0143 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1870-1609A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645634 | ||||||
chr14:56645685
|
A | G | 38 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(35): Show | 41 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1870-1558A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645685 | ||||||
chr14:56645918
|
A | G | 2 | a0005c0009t0001g0164a0005c0009t0001g0169 | 2 | HG01109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1870-1325A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645918 | ||||||
chr14:56646065
|
G | A | 1 | a0003c0007t0001g0016 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1870-1178G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56646065 | ||||||
chr14:56646104
|
T | C | 33 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(30): Show | 33 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1870-1139T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56646104 | ||||||
chr14:56646490
|
TTTTG | T | 35 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 38 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1870-746_1870-743d others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56646490 | |||||
chr14:56646555
|
C | T | 1 | a0001c0001t0005g0326 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1870-688C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56646555 | ||||||
chr14:56646783
|
G | C | 4 | a0002c0005t0013g0211a0003c0007t0013g0259a0003c0007t0013g0262others(1): Show | 4 | HG03831.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1870-460G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56646783 | ||||||
chr14:56646852
|
G | GT | 48 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(45): Show | 52 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1870-379dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56646852 | |||||
chr14:56646852
|
GT | G | 39 | a0001c0002t0001g0074a0001c0004t0003g0281a0001c0004t0003g0295others(36): Show | 39 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1870-379delT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56646852 | |||||
chr14:56646852
|
GTT | G | 37 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(34): Show | 39 | HG00621.hp1 HG01081.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.1870-380_1870-379d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56646852 | |||||
chr14:56646887
|
A | G | 4 | a0002c0005t0013g0211a0003c0007t0013g0259a0003c0007t0013g0262others(1): Show | 4 | HG03831.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1870-356A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56646887 | ||||||
chr14:56646932
|
A | T | 1 | a0001c0002t0001g0022 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1870-311A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56646932 | ||||||
chr14:56647076
|
G | A | 82 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(79): Show | 85 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(82): Show |
intron_variant | MODIFIER | c.1870-167G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56647076 | ||||||
chr14:56647098
|
T | A | 4 | a0002c0005t0013g0211a0003c0007t0013g0259a0003c0007t0013g0262others(1): Show | 4 | HG03831.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1870-145T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56647098 | ||||||
chr14:56647133
|
G | A | 33 | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(30): Show | 33 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1870-110G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56647133 | ||||||
chr14:56647178
|
T | A | 1 | a0001c0002t0001g0072 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1870-65T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56647178 |